Penam Derivatives for Treating Bacterial Infections - Patent application

Abstract

The novel iron-chelating group-conjugated penam derivatives described herein exhibit antibacterial activity and can be used as antibacterial agents or as beta-lactamase inhibitors (BLIs), which are valuable in combination with other antibacterial agents. TIFF2022548067000174.tif2637

Description

[Technical field]

[0001] This application claims priority to U.S. Provisional Patent Application No. 62 / 898,598, filed Sep. 11, 2019, entitled "Penam Derivatives for Treating Bacterial Infections," the entire contents of which are incorporated herein by reference.

[0002] The present disclosure relates to penam compounds having antibacterial or β-lactamase inhibitory activity, and to pharmaceutical compositions having said activity. [Background technology]

[0003] Penicillin antibiotics are one of the most effective modern medicines, effective against many bacterial infections. Commercially available β-lactam antibiotics are still widely used today, but their widespread use has led to the evolution of resistance in many types of bacteria. Antibiotic resistance presents a serious threat to human health (Neu, HC, 1992. Science, 257 (5073), 1064-1073; Bassetti, M. et al., 2017. Intensive care medicine, 43 (10), 1464-1475). The development of drug resistance in Gram-negative pathogens has become a major challenge worldwide. In 2017, the WHO published a prioritized list of 12 pathogens that pose the greatest threat to human health and for which new antibiotics are urgently needed. Among them, three carbapanem-resistant Gram-negative bacteria (Acinetobacter baumannii, Pseudomonas aeruginosa and Enterobacteriaceae) are prioritized as important pathogens. Summary of the Invention

[0004] The present disclosure relates generally to iron chelating group conjugated penam derivatives that are valuable for use as antibacterial compounds or as beta-lactamase inhibitors (BLIs) to enhance or restore the efficacy of beta-lactam antibacterial agents.

[0005] Inactivation of β-lactam antibiotics by β-lactamases is one of the most widespread drug resistance mechanisms among Gram-negative pathogens. Thousands of different β-lactamases have been identified worldwide. Based on their amino acid sequences, β-lactamases are classified into four classes (Ambler classification), of which A, C, and D include serine hydrolases and B includes metallo-β-lactamases.

[0006] The strategy of developing β-lactamase inhibitors to restore the antibacterial activity of β-lactams has been successful in compressing antibiotic resistance. Figure 1 shows a group of representative β-lactam ring-containing β-lactamase inhibitors. Currently, three β-lactam ring-containing β-lactamase inhibitors, clavulanic acid (1), sulbactam (2), and tazobactam (3), are used clinically to treat bacterial infections. A series of 6-alkenylpenam compounds, including compounds containing iron chelating groups such as compounds (4, LN-I-255), (5) and (6), have been reported to have β-lactamase inhibitory activity (Buynak, JD et al., 1999. Bioorganic & medicinal chemistry letters, 9(14), 1997-2002; U.S. Patent No. 8,299,051 (issued October 30, 2012)). Another iron chelating group-containing compound (7), which contains a hydroxylpyridone group as an iron chelator, has also been reported (Setti, EL et al., 1995. The Journal of antibiotics, 48 ​​(11), 1320-1329).

[0007] Low outer membrane permeability is also a major factor in antibiotic resistance in Gram-negative bacteria (Tsai, YK et al. 2011. Antimicrobial agents and chemotherapy, 55(4), 1485-1493). One way to increase drug permeability is to exploit the iron uptake pathway of Gram-negative bacteria by conjugating iron-chelating groups to antibiotics by mimicking siderophores (Mollmann, U. et al. 2009. Biometals, 22(4), 615-624). Siderophores are small, high-affinity iron-chelating compounds secreted by microorganisms such as bacteria and fungi that can bring iron into bacterial cells via specific receptors to support growth (Neilands, JB 1995. Journal of Biological Chemistry, 270(45), 26723-26726).

[0008] Conjugation of iron-chelating moieties to antibiotics has proven to be a promising solution to improve the activity of antibiotics, especially β-lactam antibiotics that are active in the periplasmic space of Gram-negative bacteria. BAL30072 (8) is an investigational siderophore (hydroxypyridone moiety) conjugated monobactam with activity against multidrug-resistant (MDR) Gram-negative bacteria (Page, MG et al., 2010. Antimicrobial agents and chemotherapy, 54(6), 2291-2302). Cefiderocol (9) is an iron-chelating group (catechol moiety) conjugated cephalosporin in late-stage clinical trials. Cefiderocol has demonstrated potent antibacterial activity against Pseudomonas aeruginosa and Acinetobacter baumannii, including carbapenem-resistant strains (Ito, A. et al., 2016. Antimicrobial agents and chemotherapy, 60(12), 7396-7401; Portsmouth, S. et al., 2018. The Lancet Infectious Diseases, 18(12), 1319-1328).

[0009] Sulbactam was initially developed as a β-lactamase inhibitor. Recently, this compound has been used to treat Acinetobacter baumannii infections, especially those caused by multidrug-resistant strains. However, resistance of Acinetobacter baumannii to sulbactam is common, especially in carbapenem-resistant clinical isolates (Karageorgopoulos, DE et al., 2008. The Lancet infectious diseases, 8(12), 751-762).

[0010] Thus, the present disclosure relates to iron chelating group-conjugated penam derivatives. The compounds exhibit antibacterial activity or are valuable for use in combination with antibiotics and may be used as beta-lactamase inhibitors (BLIs). Details of one or more embodiments of the invention are described herein. Other features, objects, and advantages of the invention will be apparent from the following description, including the claims. [Brief description of the drawings]

[0011] [Figure 1] Representative β-lactamase inhibitors are shown below.

[0012] [Diagram 2] Illustrated is Scheme A, a synthetic scheme for preparing representative compounds according to preferred embodiments disclosed herein.

[0013] [Diagram 3] Illustrated is Scheme B, a synthetic scheme for preparing representative compounds according to preferred embodiments disclosed herein.

[0014] [Figure 4] Illustrated is Scheme C, a synthetic scheme for preparing representative compounds according to preferred embodiments disclosed herein.

[0015] [Diagram 5] 1 provides synthetic schemes for preparing representative compounds according to preferred embodiments disclosed herein. [Figure 6] 1 provides synthetic schemes for preparing representative compounds according to preferred embodiments disclosed herein. [Figure 7] 1 provides synthetic schemes for preparing representative compounds according to preferred embodiments disclosed herein. [Figure 8] 1 provides synthetic schemes for preparing representative compounds according to preferred embodiments disclosed herein. [Figure 9]1 provides synthetic schemes for preparing representative compounds according to preferred embodiments disclosed herein. [Figure 10] 1 provides synthetic schemes for preparing representative compounds according to preferred embodiments disclosed herein. [Figure 11] 1 provides synthetic schemes for preparing representative compounds according to preferred embodiments disclosed herein. [Figure 12] 1 provides synthetic schemes for preparing representative compounds according to preferred embodiments disclosed herein. [Figure 13] 1 provides synthetic schemes for preparing representative compounds according to preferred embodiments disclosed herein. [Figure 14] 1 provides synthetic schemes for preparing representative compounds according to preferred embodiments disclosed herein. [Figure 15] 1 provides synthetic schemes for preparing representative compounds according to preferred embodiments disclosed herein. [Figure 16] 1 provides synthetic schemes for preparing representative compounds according to preferred embodiments disclosed herein. [Figure 17] 1 provides synthetic schemes for preparing representative compounds according to preferred embodiments disclosed herein. [Figure 18] 1 provides synthetic schemes for preparing representative compounds according to preferred embodiments disclosed herein. [Figure 19] 1 provides synthetic schemes for preparing representative compounds according to preferred embodiments disclosed herein. DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

[0016] The present disclosure relates to penam derivatives and their use as antimicrobial compounds or beta-lactamase inhibitors (BLIs).

[0017] Preferred embodiments disclosed herein include compounds of general formula I: [ka] [wherein R1 is hydrogen, a pharma- ceutically acceptable salt-forming agent, or an ester residue such as a carboxylic acid protecting group, which ester is readily metabolized or hydrolyzed in the body to form a carboxylate, including those esters; Y is independently a group selected from -S-, -SO-, and -SO2-; L is the following group: 1) (C1-C8) alkylene, 2) (C3-C8) cycloalkylene, 3) arylene, 4) heteroarylene, 5) (C3-C8)heterocycloalkylene containing 1 to 3 heteroatoms and which may be optionally unsaturated; 6) -C(=O)-, 7)-O-, 8)-S(O) n - (n is an integer 0, 1, or 2), 9)-N(R2)-, 10)-C(R3)=C(R4)-, 11) -C=N-, and wherein R2, R3 and R4 are selected from hydrogen, (C1-C8) alkyl, (C3-C8) cycloalkyl, (C1-C8) alkyloxyl, aryl, heteroaryl, or (C3-C8) heterocycloalkyl; R3 and R4 together may form a bond, and a carbon or nitrogen atom of the linker group may be optionally substituted with 1 to 3 substituents; Z is [ka] or [ka] an iron chelating moiety having at least two hydroxyl groups selected from: wherein R5, R6 and R7 are independently a group selected from hydrogen, hydroxyl, halogen, nitrile, nitro, amino, CF3, OCF3, alkyl, alkylamino, alkoxy, aryl, heteroaryl; Two of the three substituents R5, R6 and R7 may optionally be joined together to form an optionally substituted 5-8 membered ring. or a stereoisomer, a pharma- ceutically acceptable salt, a solvate, a prodrug, or a deuterium-exchanged compound thereof.

[0018] In a further preferred embodiment of the penam derivatives of general formula I above, Y is -SO2-.

[0019] In a further preferred embodiment of the penam derivatives of general formula I above, L is: -CH=NN(R2)-X-, -CH2OC(O)-N(R2)-X-, -CH=NOX-, -CH2OC(O)-X-, -CH2N(R2)-X-, [ka] Selected from Where X is: i) (C1-C8) alkylene, ii) (C3-C8)cycloalkylene; iii) (C3-C8)heterocycloalkylene; iv) arylenes, v) heteroarylene, vi) -O-, vii) -N(R2)-, and viii)-C(O)- is selected from a combination of 1 to 5 groups selected from where R2 is as defined above.

[0020] In a further preferred embodiment of the penam derivatives of general formula I above, Z is: [ka] [ka] is selected from.

[0021] Further preferred embodiments of the penam derivatives are identified in Table 1 below. Table 1 [Table 1] [Table 2] [Table 3]

[0022] [Table 4] [Table 5] [Table 6]

[0023] [Table 7] [Table 8] [Table 9]

[0024] [Table 10] [Table 11] [Table 12]

[0025] [Table 13] [Table 14] [Table 15]

[0026] [Table 16] [Table 17] [Table 18]

[0027] The terms and phrases used herein have meanings and definitions as known in the art. Some of the more commonly used phrases are described in more detail below.

[0028] The amount of carbon atoms in various hydrocarbon-containing moieties is indicated by prefixes that specify the minimum and maximum number of carbon atoms in the moiety, i.e., the prefix C i -C j represents the portion of carbon atoms from integer "i" to integer "j," inclusive. Thus, for example, C1-C6 alkyl refers to alkyl of 1 to 6 carbon atoms, inclusive.

[0029] The term "alkyl" as used herein refers to a monovalent radical of a saturated straight or branched chain hydrocarbon group. Examples of alkyl groups include methyl, ethyl, propyl, isopropyl, n-butyl, isobutyl, tert-butyl, neopentyl, and n-hexyl. The alkyl groups of the present invention may be optionally substituted. Preferred alkyl groups of the present invention have 1 to 8 carbons. The alkyl groups of the present invention may be optionally substituted.

[0030] The term "alkenyl" as used herein refers to a monovalent radical of an unsaturated straight or branched chain hydrocarbon group having at least one C=C double bond. Examples of alkenyl groups include allyl or propenyl, butenyl, isobutenyl, pentenyl, and the like. Alkenyl groups of the present invention may be optionally substituted.

[0031] The term "alkynyl" as used herein refers to a monovalent radical of an unsaturated straight or branched chain hydrocarbon group having at least one C≡C triple bond. Examples of alkynyl groups include propargyl, butynyl, isobutynyl, pentynyl, and the like. Alkynyl groups of the present invention can be optionally substituted.

[0032] The terms "alkylene", "alkenylene" or "alkynylene" as used herein refer to a divalent radical of an alkyl, alkenyl, or alkynyl group, as defined above. Examples of alkylene groups include methylene, ethylene, propylene, isopropylene, n-butylene, isobutylene, n-hexylene, and the like. Examples of alkenylene groups include ethenylene, propenylene, and the like. Examples of alkynylene groups include ethynylene, propynylene, and the like. The "alkylene", "alkenylene" or "alkynylene" groups of the present invention may be optionally substituted.

[0033] The term "alkylamino" as used herein refers to an amino group (-NH2) in which one hydrogen atom has been replaced by an alkyl group. Examples of alkylamino include methylamino, ethylamino, propylamino, and isopropylamino.

[0034] The term "alkoxy" as used herein refers to an alkyl group, as defined above, attached to an oxygen atom. Examples of alkoxy include methoxy, ethoxy, propoxy, isopropoxy, n-butoxy, tert-butoxy, neo-pentoxy and n-hexyloxy. The alkoxy groups of the present invention may be optionally substituted.

[0035] As used herein, the term "aryl" refers to a monovalent radical of a carbocyclic aromatic group, including phenyl, naphthyl, and anthracenyl. The aryl groups of this invention can be optionally substituted.

[0036] The term "arylene," as used herein, refers to a divalent radical of an optionally substituted aryl group, as defined above, such as phenylene.

[0037] As used herein, the term "cycloalkyl" refers to a monovalent radical of a saturated carbocyclic group having three to eight carbons, such as cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, and cyclooctyl. The cycloalkyl groups of the present invention can be optionally substituted.

[0038] The term "cycloalkylene," as used herein, refers to a divalent radical of a saturated carbocyclic ring group having from 3 to 8 carbons. The cycloalkylene groups of the present invention can be optionally substituted.

[0039] As used herein, the term "halogen" or "halide" refers to fluorine, chlorine, bromine, and iodine atoms, and the term "halo" refers to --F, --Cl, --Br, and --I as a substituent.

[0040] The term "heteroaryl" as used herein refers to a cyclic aromatic group having 5 or 6 ring atoms, in which at least one ring atom is selected from the group consisting of oxygen, sulfur and nitrogen, and the remaining ring atoms are carbon. Heteroaryl groups of the present invention include groups derived from furan, imidazole, isothiazole, isoxazole, oxazole, pyrazine, pyrazole, pyridazine, pyridine, pyrimidine, pyrrole, quinoline, thiazole, 1,3,4-thiadiazole, triazole, and tetrazole. Heteroaryl groups of the present invention may be optionally substituted.

[0041] As used herein, the term "heteroarylene" refers to a divalent cyclic aromatic group having five or six ring atoms, in which at least one ring atom is selected from the group consisting of oxygen, sulfur and nitrogen, and the remaining ring atoms are carbon. Heteroarylene groups may be optionally substituted.

[0042] The term "heteroatom" as used herein refers to an oxygen, nitrogen, or sulfur atom.

[0043] The term "heterocycloalkyl" as used herein refers to a non-aromatic 5-, 6-, 7-, or 8-membered ring or bi- or tricyclic group having one or more heteroatoms independently selected from oxygen, sulfur, and nitrogen, where each 5-membered ring has 0 to 1 double bond and each 6-membered ring has 0 to 2 double bonds. The nitrogen and sulfur heteroatoms may be optionally oxidized, the nitrogen heteroatom may be optionally quaternized, and any of the above heterocyclic rings may be fused to an aryl or heteroaryl ring. Representative heterocycloalkyls include, but are not limited to, pyrrolidinyl, pyrazolinyl, pyrazolidinyl, imidazolinyl, imidazolidinyl, piperidinyl, piperazinyl, oxazolidinyl, isoxazolidinyl, morpholinyl, thiazolidinyl, morpholinyl, isothiazolidinyl, and tetrahydrofuranyl.Heterocycloalkyl groups of the invention may optionally be -F, -Cl, -OH, -NO2, -CN, -C(O)-alkyl, -C(O)-aryl, -C(O)-heteroaryl, -CO2-alkyl, -CO2-aryl, -CO2-heteroaryl, -C(O)NH2, -C(O)NH-alkyl, -C(O)NH-aryl, -C(O)NH-heteroaryl, -OC(O)-alkyl, -OC(O)-aryl, -OC(O)-heteroaryl, -OC(O)NH2, -OC(O)NH-alkyl, -OC(O)NH-aryl, -OCONH-heteroaryl, -NHC(O)-alkyl, -NHC(O)-aryl, -NHC(O)-heteroaryl, -NHCO2-alkyl, -NHCO2-aryl, -NHCO2-heteroaryl, -NHC(O)NH2, -NHC(O)NH-alkyl, -NHC and optionally substituted by one, two or three substituents independently selected from (O)NH-aryl, -NHC(O)NH-heteroaryl, -SO2-alkyl, -SO2-aryl, -SO2-heteroaryl, -SON2NH2, -SON2NH-alkyl, -SON2NH-aryl, -SON2NH-heteroaryl, -alkyl, -cycloalkyl, -cycloheteroalkyl, -CF3, -CH2OH, -CH2NH2, -aryl, -heteroaryl, -benzyl, -benzyloxy, -aryloxy, -heteroaryloxy, -alkoxy, -methoxymethoxy, -methoxyethoxy, -amino, -benzylamino, -arylamino, -heteroarylamino, -alkylamino, -thio, -arylthio, -heteroarylthio, -benzylthio, -alkylthio, or -methylthiomethyl.

[0044] The term "heterocycloalkylene" as used herein refers to a divalent heterocycloalkyl group, as defined above. The heterocycloalkylene groups of the present invention may be optionally substituted.

[0045] The term "hydroxyl" as used herein refers to --OH.

[0046] As used herein, the term "substituted" refers to one or more substituents being covalently attached.

[0047] The term "prodrug" as used herein refers to a prodrug of a compound of the present invention that is suitable for use in humans and animals with acceptable toxicity, irritation, allergic reactions, etc., and is effective for its intended use, commensurate with a reasonable benefit-to-risk ratio. As used herein, the term "prodrug" refers to a compound that can be converted in vivo into the parent compound as defined above.

[0048] The term "salt" as used herein refers to those salts that are suitable for use in humans and animals with acceptable toxicity, irritation, allergic reactions, etc., and are commensurate with a reasonable benefit-to-risk ratio. Pharmaceutically acceptable salts are well known in the art. The salts can be prepared by reacting the compounds of the present invention with an acid or base (an agent that forms a pharma-ceutically acceptable salt), or can be prepared in situ during the final isolation step. Examples of pharma-ceutically acceptable salts are salts of acid groups formed with inorganic bases such as sodium hydroxide, sodium carbonate, sodium phosphate, etc. Examples of pharma-ceutically acceptable salts are salts of amino groups formed with inorganic acids such as hydrochloric acid, hydrobromic acid, phosphoric acid, and sulfuric acid, or organic acids such as acetic acid, oxalic acid, maleic acid, tartaric acid, citric acid, succinic acid, or malonic acid. Other metal salts include lithium, potassium, calcium, and magnesium. Further pharma- ceutically acceptable salts include ammonium cations formed with counterions such as halides, hydroxides, carboxylates, sulfates, phosphates, nitrates, lower alkylsulfonates, and arylsulfonates.

[0049] The term "solvate" as used herein refers to a compound in which the solvent is bound in molecular form, i.e., the solvent is coordinately bonded, and can be represented, for example, by the formula R·(solvent), where R is a compound disclosed herein. A given compound may form one or more solvates, including, for example, monosolvates (R·(solvent)), or multiple solvates (R·n(solvent)), including, for example, disolvates (R·2(solvent)), trisolvates (R·3(solvent)), etc., where n is an integer greater than 1, or hemisolvates, for example, R·n / 2(solvent), R·n / 3(solvent), R·n / 4(solvent), etc., where n is an integer. Solvents herein include mixed solvents, e.g., methanol / water, and thus solvates may incorporate one or more solvents within the solvate.

[0050] As used herein, the term "deuterium exchanged compound" refers to a compound in which one or more hydrogen atoms have been replaced with deuterium atoms. Deuterated compounds can be produced chemically in reactions with deuterium oxide, or biologically by growing organisms such as bacteria in media containing deuterium oxide, or by growing plants by replacing their water source with deuterium oxide.

[0051] The term "agent that forms a pharma-ceutically acceptable salt" as used herein refers to an acid or base that can react with the compound of the present invention to form a pharma-ceutically acceptable salt. Examples of bases are inorganic bases such as sodium hydroxide, sodium carbonate, or sodium phosphate, and organic bases such as pyridine, triethylamine, or N,N-diisopropylmethylamine. Examples of acids are inorganic acids such as hydrochloric acid, hydrobromic acid, phosphoric acid, and sulfuric acid, or organic acids such as acetic acid, oxalic acid, maleic acid, tartaric acid, citric acid, succinic acid, or malonic acid.

[0052] Compounds that have the same molecular formula but differ in the nature or sequence of bonding of their atoms or in the arrangement of their atoms in space are called "isomers". Isomers that differ in the arrangement of their atoms in space are called "stereoisomers". Stereoisomers that are not mirror images of each other are called "diastereomers", and isomers that are non-superimposable mirror images of each other are called "enantiomers". When a compound has an asymmetric center, for example, when a carbon atom is bonded to four different groups, a pair of enantiomers is possible. Enantiomers are characterized by the absolute configuration of their asymmetric center and are described according to the R- and S-sequencing rules of Cahn and Prelog, or by the way the molecule rotates the plane of polarized light and are called dextrorrotatory or levorotatory (i.e., (+) or (-)-isomers, respectively). Chiral compounds can exist as individual enantiomers or as mixtures thereof. A mixture containing equal proportions of enantiomers is called a "racemic mixture". The compounds of the present invention may possess one or more asymmetric centers; thus, such compounds may be produced as individual (R)- or (S)-stereoisomers, or as mixtures thereof. Unless otherwise specified, the description or name of a particular compound in the specification and claims is intended to encompass both individual enantiomers, and vice versa, mixtures thereof, racemates.

[0053] "Pharmaceutically acceptable carrier" means a carrier that is generally safe, non-toxic, biologically or otherwise desirable and useful in preparing pharmaceutical compositions, and includes carriers that are acceptable for veterinary use, as well as for human pharmaceutical use. As used in the specification and claims, "pharmaceutically acceptable carrier" includes both one and more than one such carrier.

[0054] "Treating" a disease or "treatment" of a disease includes preventing the disease, i.e., causing clinical symptoms of the disease to not develop in a mammal that is exposed to or susceptible to the disease but that has not yet experienced or displayed symptoms of the disease; inhibiting the disease, i.e., arresting or reducing the onset of the disease or its clinical symptoms; or alleviating the disease, i.e., causing regression of the disease or its clinical symptoms.

[0055] "Therapeutically effective amount" means the amount of a compound that, when administered to a mammal for treating a disease, is sufficient to effect such treatment for the disease. The "therapeutically effective amount" will vary depending on the compound, the disease and its severity, and the age, weight, etc., of the mammal being treated.

[0056] The compounds of the present invention are generally named according to the IUPAC or CAS nomenclature system. Abbreviations well known to those skilled in the art may be used (e.g., "Ph" for phenyl, "Me" for methyl, "Et" for ethyl, "h" for hours, and "rt" for room temperature).

[0057] The compounds of the preferred embodiments described herein can be better understood in connection with their synthetic schemes. The synthetic procedures of Schemes A to C shown in Figures 2 to 4 are for illustrative purposes and are not intended to limit the scope of the invention. It will be apparent to those skilled in the art that the compounds of the present invention can be prepared by various synthetic routes, including, but not limited to, substituting appropriate reagents, solvents or catalysts, changing the reaction sequence, and converting protecting groups.

[0058] Scheme A shown in Figure 2 illustrates the preparation of a preferred embodiment of the penam derivative compound of formula I described herein. (2S,3R,5R)-benzhydryl 3-formyl-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate 4,4-dioxide (1A, synthesis reported in US Patent No. 5,686,441) is an important starting aldehyde that can be reacted with hydrazides or substituted hydrazides (2A) bearing different iron chelating moieties via a condensation reaction to give compounds (3A). A series of compounds of formula I (4A) can be synthesized by deprotecting the protecting group of (3A).

[0059] Scheme B shown in Figure 3 illustrates the preparation of another set of preferred embodiments of the penam derivative compounds of formula I disclosed herein. (2S,3R,5R)-benzhydryl-3-methyl-3-((((4-nitrophenoxy)carbonyl)oxy)methyl)-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate 4,4-dioxide (3B) is prepared by reacting (1B) (a known compound reported in Hyodo, A. et al., 1996. The Journal of Antibiotics, 49 (9), 944-946) with 4-nitrophenyl carbonochloridate (2B) via a displacement reaction. Compound (3B) is a key intermediate with a leaving group for the next step (see US Pat. 2010 / 9954 A1; US ​​Pat. No. 8,299,051 B2; US Pat. 2013 / 79318 A1; US ​​Pat. No. 8,575,144 B2 for the synthesis of compounds similar to 3B), which can be reacted with several nucleophilic compounds (4B) via substitution reaction to give compounds (5B). Compound (4B) is selected from hydrazides or substituted hydrazides with iron chelating moieties; primary amines, secondary amines or cyclic amines with iron chelating moieties. A series of compounds of formula I (6B) can be synthesized via deprotection of the protecting group of (5B).

[0060] Scheme C shown in Figure 4 illustrates the preparation of yet another set of preferred embodiments of the penam derivative compounds of formula I disclosed herein. (2S,3R,5R)-benzhydryl-3-((E)-(hydroxyimino)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate 4,4-dioxide (1C) (known compound reported in Phillips, OA et al., 2005. Bioorganic & medicinal chemistry, 13(8), 2847-2858) is reacted with NCS to give (2S,3R,5R)-benzhydryl-3-((Z)-chloro(hydroxyimino)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate 4,4-dioxide (2C). Cyclization of (2C) with (3C) gives intermediate compound (4C), which is an alkene or alkyne bearing an iron chelating moiety. A series of compounds of formula I (5C) can be synthesized by deprotecting the protecting group of (4C).

[0061] The preferred embodiments described herein also include pharmaceutical compositions comprising a pharma- ceutical effective amount of a penam derivative compound of formula I in combination with a pharma- ceutical acceptable carrier, optionally in combination with other antibacterial agents.

[0062] Preferred embodiments described herein also include methods of treating or preventing a microbial infection in a subject in need of treatment by administering a pharmaceutical composition of formula I.

[0063] Preferred embodiments of the pharmaceutical compositions of the present invention comprise a therapeutically effective amount of a compound of the penam derivative described herein, formulated with one or more pharma- ceutical acceptable carriers, such as injectable preparations or sterile injectable solutions, compositions for rectal or vaginal administration, liquid or solid dosage forms for oral administration, dosage forms for topical or transdermal administration, powders and sprays.

[0064] In accordance with the methods of treatment using the penam derivative compounds described herein, bacterial infections are treated or prevented in a patient, such as a human or animal, by administering to the patient a therapeutically effective amount of a compound of the invention in an amount and for a period of time necessary to achieve the desired therapeutic effect.

[0065] A preferred embodiment of the compounds of the present invention are the penam derivatives of formula I as specified above. In one aspect, the compounds of the present invention contain several asymmetric and geometric centers. In some cases, one or more of the asymmetric and geometric centers can be converted to their opposite configuration. These stereoisomers are within the scope of the present invention. The examples are merely illustrative and are not intended to limit the scope of the present invention.

[0066] The abbreviations used herein have the meanings known to those skilled in the art, specifically, Ac stands for acetyl group, Boc stands for t-butoxycarbonyl group, Bn stands for benzyl group, Cbz stands for benzyloxycarbonyl group, DCM stands for dichloromethane, DMAP stands for 4-N,N-dimethylaminopyridine, DMF stands for N,N-dimethylformamide, DMSO stands for dimethylsulfoxide, EDCI stands for 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride, Et stands for ethyl group, EtOAc stands for acetic acid. Ethyl is ethyl, EtOH is ethanol, HOBT is 1-hydroxybenzotriazole, Me is methyl, NCS is N-chlorosuccinimide, NMM is N-methylmorpholine, OMe is methoxyl, PE is petroleum ether, PMB is para-methoxybenzyl, Ph is phenyl, Pr is propyl, TEA is triethylamine, TFA is trifluoroacetic acid, and THF is tetrahydrofuran. The following abbreviations are also used: millimole (mmol), milliliter (mL), milligram (mg), microliter (μL), and microgram (μg).

[0067] (Example) The following examples describe how to make various compounds and how to carry out various methods of the present invention and are to be construed as merely illustrative and not limiting the preceding disclosure in any way whatsoever. Those skilled in the art will recognize appropriate variations from the procedures, both with respect to reagents and with respect to reaction conditions and techniques.

[0068] Example 1 (2S,3R,5R)-3-((E)-(2-(2-chloro-4,5-dihydroxybenzoyl)hydrazono)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0069] FIG. 5 shows a synthetic scheme for preparing this compound. Step 1: (2S,3R,5R)-Benzhydryl 3-((E)-(2-(2-chloro-4,5-dihydroxybenzoyl)hydrazono)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate 4,4-dioxide To a solution of (3R,5R)-benzhydryl 3-formyl-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate 4,4-dioxide (1.7 g, 4.1 mmol) in DCM (10 mL) and EtOH (10 mL) was added 2-chloro-4,5-dihydroxybenzohydrazide (0.87 g, 4.3 mmol). The mixture was stirred at room temperature for 6 hours. The solvent was then evaporated under vacuum and the residue was purified by flash chromatography (DCM:MeOH=20:1) to give the title product (1.0 g, 41% yield) as a white solid. MS(ESI): m / z=598(M+H) +

[0070] Step 2: (2S,3R,5R)-3-((E)-(2-(2-chloro-4,5-dihydroxybenzoyl)hydrazono)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide A solution of (2S,3R,5R)-benzhydryl 3-((E)-(2-(2-chloro-4,5-dihydroxybenzoyl)hydrazono)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate 4,4-dioxide (1.0 g, 1.7 mmol) in m-cresol (5 mL) was stirred at 50° C. for 5 hours. The solution was poured into PE (10 mL). The solid obtained by filtration was purified by column chromatography (silica gel, DCM:MeOH=20:1) to give a white solid (400 mg, 56% yield). 1 H NMR (400MHz, DMSO-d6)δ 12.10(s,H), 10.20(s,1H), 9.41(s,1H), 7.79(s,1H), 7.12(s,1H), 6.94(d,1H), 6.83(d,1H), 6.62(s,1H), 5.30(d,1H), 5.01(s,1H), 3.74(t,3H), 3.31(m,1H), 2.20(s,1H), 1.62(s,3H);LC-MS(ESI):m / z=432(M+H) +

[0071] Example 2 (2S,3R,5R)-3-Methyl-7-oxo-3-((E)-(2-(2,3,4-trihydroxybenzoyl)hydrazono)methyl)-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0072] The title compound was prepared using a similar procedure as described in Example 1, except using 2,3,4-trihydroxybenzohydrazide instead of 2-chloro-4,5-dihydroxybenzohydrazide. 1H NMR (400MHz, DMSO-d6)δ 13.84(br,1H), 12.08(s,1H), 12.05(s,1H), 9.79(s,1H), 8.61(s,1H), 7.92(s,1H), 7.31(d,1H), 6.39( d,1H), 5.28(d,1H), 4.90(s,1H), 3.72(dd,1H), 3.26(dd,1H), 1.61(s,3H);LC-MS(ESI):m / z=414(M+H) +

[0073] Example 3 (2S,3R,5R)-3-((E)-(2-(2-chloro-3,4-dihydroxybenzoyl)-2-methylhydrazono)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0074] The title compound was prepared using a similar procedure as described in Example 1, except using 2-chloro-3,4-dihydroxy-N-methylbenzohydrazide instead of 2-chloro-4,5-dihydroxybenzohydrazide.

[0075] 1 H NMR (400MHz, DMSO-d6)δ 13.81(br,1H), 9.98(s,1H), 9.19(s,1H), 7.44(s,1H), 6.75(d,1H), 6.61(d,1H), 5.16(d,1H), 4.68(d,1H), 4.57(s,1H), 4.54(d,1H), 3.61(dd,1H), 3.31(s,3H), 3.26(dd,1H), 1.61(s,3H);LC-MS(ESI):m / z=446(M+H) +

[0076] Example 4 (2S,3R,5R)-3-((E)-(2-(2,5-dichloro-3,4-dihydroxybenzoyl)hydrazono)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0077] The title compound was prepared using a similar procedure as described in Example 1, except using 2,5-dichloro-3,4-dihydroxybenzohydrazide instead of 2-chloro-4,5-dihydroxybenzohydrazide. 1 H NMR (400MHz, DMSO-d6)δ 13.88(br,1H), 12.13(s,1H), 10.08(br,2H), 7.74(s,1H), 7.15(s,1H), 5.29(d,1H) , 4.90(s,1H), 3.78(dd,1H), 3.26(dd,1H), 1.61(s,3H);LC-MS(ESI):m / z=466(M+H) +

[0078] Example 5 (2S,3R,5R)-3-((E)-(2-(3,4-dihydroxybenzoyl)hydrazono)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0079] The title compound was prepared using a similar procedure as described in Example 1, except using 3,4-dihydroxybenzohydrazide instead of 2-chloro-4,5-dihydroxybenzohydrazide.

[0080] 1H NMR (400MHz, DMSO-d6):δ 13.84(br,1H), 11.92(s,1H), 9.69(s,1H), 9.27(s,1H), 7.90(s,1H), 7.34(s,1H), 7.29(d,1H), 6.82( d,1H), 5.28(d,1H), 4.90(s,1H), 3.72(dd,1H), 3.26(dd,1H), 1.61(s,3H);LC-MS(ESI):m / z=398(M+H) +

[0081] Example 6 (2S,3R,5R)-3-Methyl-7-oxo-3-((E)-(2-(3,4,5-trihydroxybenzoyl)hydrazono)methyl)-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0082] The title compound was prepared using a similar procedure as described in Example 1, except using 3,4,5-trihydroxybenzohydrazide instead of 2-chloro-4,5-dihydroxybenzohydrazide.

[0083] 1 H NMR (400MHz, DMSO-d6)δ 13.79(br,1H), 11.90(s,1H), 9.21(s,2H), 7.88(s,1H), 6.90(s,2H), 5.28(d,1H), 4.90(s,1H), 3.72(dd,1H), 3.26(dd,1H), 1.61(s,3H);LC-MS(ESI):m / z=414(M+H) +

[0084] Example 7 (2S,3R,5R)-3-((E)-(2-(3,4-dihydroxybenzoyl)-2-methylhydrazono)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0085] The title compound was prepared using a similar procedure as described in Example 1, except using 3,4-dihydroxy-N-methylbenzohydrazide instead of 2-chloro-4,5-dihydroxybenzohydrazide.

[0086] 1 H NMR (400MHz, DMSO-d6)δ 13.83(br,1H), 9.54(s,1H), 9.11(s,1H), 7.42(s,1H), 7.13(s,1H), 7.05(d,1H), 6.71(d,1H), 5.16(d,1H), 4.68(d ,1H), 4.57(s,1H), 4.54(d,1H), 3.61(dd,1H), 3.34(s,3H), 3.26(dd,1H), 1.61(s,3H);LC-MS(ESI):m / z=412(M+H) +

[0087] Example 8 (2S,3R,5R)-3-((E)-(2-(2-hydroxy-3-methylbenzoyl)hydrazono)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0088] The title compound was prepared using a similar procedure as described in Example 1, except using 2-hydroxy-3-methylbenzohydrazide instead of 2-chloro-4,5-dihydroxybenzohydrazide. 1H NMR (400MHz, DMSO-d6)δ 13.84(br,1H), 12.38(s,1H), 12.32(s,1H), 7.98(s,1H), 7.78(d,1H), 7.39(d,1H), 8.86(t,1H), 5.29( d,1H), 4.90(s,1H), 3.78(dd,1H), 3.26(dd,1H), 2.18(s,3H), 1.61(s,3H);LC-MS(ESI):m / z=396(M+H) +

[0089] Example 9 (2S,3R,5R)-3-((E)-(2-(2-hydroxybenzoyl)hydrazono)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0090] The title compound was prepared using a similar procedure as described in Example 1, except using 2-hydroxybenzohydrazide instead of 2-chloro-4,5-dihydroxybenzohydrazide. 1 H NMR (400MHz, DMSO-d6)δ 13.84(br,1H), 12.09(s,1H), 11.52(s,1H), 7.97(s,1H), 7.83(d,1H), 7.48(t,1H), 6.97(dd,2H) , 5.29(d,1H), 4.90(s,1H), 3.78(dd,1H), 3.26(dd,1H), 1.61(s,3H);LC-MS(ESI):m / z=382(M+H) +

[0091] Example 10 (2S,3R,5R)-3-((E)-(2-(2-bromo-3,4-dihydroxybenzoyl)hydrazono)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0092] The title compound was prepared using a similar procedure as described in Example 1, except using 2-bromo-3,4-dihydroxybenzohydrazide instead of 2-chloro-4,5-dihydroxybenzohydrazide. 1 H NMR (400MHz, DMSO-d6)δ 13.82(br,1H), 11.97(s,1H), 10.21(s,1H), 9.38(s,1H), 7.72(s,1H), 6.81(d,2H), 5.29( d,1H), 4.90(s,1H), 3.78(dd,1H), 3.26(dd,1H), 1.61(s,3H);LC-MS(ESI):m / z=476(M+H) +

[0093] Example 11 (2S,3R,5R)-3-Methyl-7-oxo-3-((E)-(2-(2,3,6-trichloro-4,5-dihydroxybenzoyl)hydrazono)methyl)-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0094] The title compound was prepared using a similar procedure as described in Example 1, except using 2,3,6-trichloro-4,5-dihydroxybenzohydrazide instead of 2-chloro-4,5-dihydroxybenzohydrazide. 1 H NMR (400MHz, DMSO-d6)δ 13.91(br,1H), 12.37(s,1H), 7.71(s,1H), 5.14(d,1H), 5.00(s,1H), 3.78(dd,1H), 3.26(dd,1H), 1.61(s,3H);LC-MS(ESI):m / z=500(M+H) +

[0095] Example 12 (2S,3R,5R)-3-((E)-(2-isonicotinoylhydrazono)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0096] The title compound was prepared using a similar procedure as described in Example 1, except using isonicotinohydrazide instead of 2-chloro-4,5-dihydroxybenzohydrazide. 1 H NMR (400MHz, DMSO-d6)δ 13.76(br,1H), 12.42(s,1H), 8.79(d,2H), 7.98(s,1H), 7.80(d,2H), 5.23(d,1H), 4.89(s,1H), 3.73(dd,1H), 3.32(dd,1H), 1.63(s,3H);LC-MS(ESI):m / z=367(M+H) +

[0097] Example 13 (2S,3R,5R)-3-Methyl-3-((E)-(2-nicotinoylhydrazono)methyl)-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0098] The title compound was prepared using a similar procedure as described in Example 1, except using nicotinohydrazide instead of 2-chloro-4,5-dihydroxybenzohydrazide. 1 H NMR (400MHz, DMSO-d6)δ 13.76(br,1H), 8.33(d,2H), 7.62(s,1H), 7.22(br,1H), 7.02(t,1H), 6.55(s,1H), 5.23( d,1H), 4.89(s,1H), 3.73(dd,1H), 3.32(dd,1H), 1.63(s,3H);LC-MS(ESI):m / z=367(M+H)+

[0099] Example 14 (2S,3R,5R)-3-((E)-(2-(2,6-dichloro-3,4-dihydroxybenzoyl)hydrazono)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0100] The title compound was prepared using a similar procedure as described in Example 1, except using 2,6-dichloro-3,4-dihydroxybenzohydrazide instead of 2-chloro-4,5-dihydroxybenzohydrazide. 1 H NMR (400MHz, DMSO-d6)δ 14.00(br,1H), 12.15(s,1H), 10.40(s,1H), 10.13(s,1H), 7.72(s,1H), 6.88(s,1H), 5.29 (d,1H), 4.90(s,1H), 3.78(dd,1H), 3.26(dd,1H), 1.61(s,3H);LC-MS(ESI):m / z=466(M+H) +

[0101] Example 15 (2S,3R,5R)-3-((E)-(2-(2-fluoro-3,4-dihydroxybenzoyl)hydrazono)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0102] The title compound was prepared using a similar procedure as described in Example 1, except using 2-fluoro-3,4-dihydroxybenzohydrazide instead of 2-chloro-4,5-dihydroxybenzohydrazide. 1H NMR (400MHz, DMSO-d6)δ 13.89(br,1H), 11.88(s,1H), 10.12(s,1H), 9.33(s,1H), 7.81(s,1H), 6.98(s,1H), 6.88(d,1H) , 5.29(d,1H), 4.90(s,1H), 3.78(dd,1H), 3.26(dd,1H), 1.61(s,3H);LC-MS(ESI):m / z=416(M+H) +

[0103] Example 16 (2S,3R,5R)-3-((E)-(2-(3,4-dihydroxy-2-methylbenzoyl)hydrazono)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0104] The title compound was prepared using a similar procedure as described in Example 1, except using 3,4-dihydroxy-2-methylbenzohydrazide instead of 2-chloro-4,5-dihydroxybenzohydrazide. 1 H NMR (400MHz, DMSO-d6)δ 13.69(br,1H), 11.83(s,1H), 9.73(s,1H), 8.44(s,1H), 7.78(s,1H), 6.78(d,1H), 6.67(dd,1H), 5.28( s,1H), 4.85(s,1H), 3.78(dd,1H), 3.26(dd,1H), 2.17(s,3H), 1.61(s,3H);LC-MS(ESI):m / z=412(M+H) +

[0105] Example 17 (2S,3R,5R)-3-Methyl-7-oxo-3-((E)-(2-picolinoylhydrazono)methyl)-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0106] The title compound was prepared using a similar procedure as described in Example 1, except using picolinohydrazide instead of 2-chloro-4,5-dihydroxybenzohydrazide. 1 H NMR (400MHz, DMSO-d6)δ 13.79(br,1H), 12.51(s,1H), 8.71(d,1H), 8.16(s,1H), 8.11(d,1H), 8.06(t,1H), 7.69(t,1H), 5.23(d,1H), 4.89(s,1H), 3.73(dd,1H), 3.32(dd,1H), 1.63(s,3H);LC-MS(ESI):m / z=367(M+H) +

[0107] Example 18 (2S,3R,5R)-3-Methyl-7-oxo-3-((E)-(2-(pyrimidine-5-carbonyl)hydrazono)methyl)-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0108] The title compound was prepared using a similar procedure as described in Example 1, except using pyrimidine-5-carbohydrazide instead of 2-chloro-4,5-dihydroxybenzohydrazide. 1 H NMR (400MHz, DMSO-d6)δ 13.75(br,1H), 9.35(s,1H), 9.09(d,1H), 8.12(s,1H), 8.07(d,1H), 5.23(d,1H), 4.89(s,1H), 3.73(dd,1H), 3.32(dd,1H), 1.63(s,3H);LC-MS(ESI):m / z=368(M+H) +

[0109] Example 19 (2S,3R,5R)-3-Methyl-7-oxo-3-((E)-(2-(pyrazine-2-carbonyl)hydrazono)methyl)-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0110] The title compound was prepared using a similar procedure as described in Example 1, except using pyrazine-2-carbohydrazide instead of 2-chloro-4,5-dihydroxybenzohydrazide. 1 H NMR (400MHz, DMSO-d6)δ 13.83(br,1H), 9.22(d,1H), 8.91(d,1H), 8.78(s,1H), 8.12(s,1H), 5.23(d,1H), 4.89(s,1H), 3.67(dd,1H), 3.31(dd,1H), 1.61(s,3H);LC-MS(ESI):m / z=368(M+H) +

[0111] Example 20 (2S,3R,5R)-3-((E)-(2-(2-(3,4-dihydroxyphenyl)acetyl)hydrazono)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0112] The title compound was prepared using a similar procedure as described in Example 1, except using 2-(3,4-dihydroxy-2-methylphenyl)acetohydrazide instead of 2-chloro-4,5-dihydroxybenzohydrazide. 1H NMR (400MHz, DMSO-d6)δ 13.73(br,1H), 11.81(s,1H), 8.87(s,1H), 8.74(s,1H), 7.70(s,1H), 6.68(d,1H), 6.61(dd,1H), 6.51(dd,1H), 5.28 (d,1H), 4.90(s,1H), 3.72(d,1H), 3.61(dd,1H), 3.31(d,1H), 3.26(dd,1H), 1.61(s,3H);LC-MS(ESI):m / z=412(M+H) +

[0113] Example 21 (2S,3R,5R)-3-((E)-(2-((R)-2-((tert-butoxycarbonyl)amino)-3-(3,4-dihydroxyphenyl)propanoyl)hydrazono)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0114] The title compound is 2-chloro-4,5-dihydroxybenzohydrazide. This was prepared using a procedure similar to that described in Example 1, except that (R)-tert-butyl (3-(3,4-dihydroxy-2-methylphenyl)-1-hydrazinyl-1-oxopropan-2-yl)carbamate was used instead of (R)-tert-butyl (3-(3,4-dihydroxy-2-methylphenyl)-1-hydrazinyl-1-oxopropan-2-yl)carbamate. 1 H NMR (400MHz, DMSO-d6)δ 13.75(br,1H), 11.62(s,1H), 8.68(br,2H), 7.73(s,1H), 7.64(s,1H), 7.06(d,1H), 6.51(d,1H), 5.28(d,1H), 4.90(s,1H), 3.72(d,1H), 3.61(dd,1H), 3.26(dd,1H), 4.80(m,1H), 3.71(br,1H), 2.74(m,1H), 2.59(d,1H), 1.61(s,3H), 1.10(s,9H);LC-MS(ESI):m / z=541(M+H) +

[0115] Example 22 (2S,3R,5R)-3-((E)-(2-(3-chloro-4,5-dihydroxybenzoyl)hydrazono)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0116] The title compound was prepared using a similar procedure as described in Example 1, except using 3-chloro-4,5-dihydroxybenzohydrazide instead of 2-chloro-4,5-dihydroxybenzohydrazide. 1 H NMR (400MHz, DMSO-d6)δ 12.11(s,H), 10.20(s,1H), 9.41(s,1H), 7.83(s,1H), 7.10(s,1H), 6.92(d,1H), 6.82(d,1H), 6.64(s,1H), 5.28(d,1H), 5.01(s,1H), 3.73(t,3H), 3.33(m,1H), 2.20(s,1H), 1.62(s,3H);LC-MS(ESI):m / z=432(M+H) +

[0117] Example 23 (2S,3R,5R)-3-((E)-(2-(2-chloro-3,4-dihydroxybenzoyl)hydrazono)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0118] The title compound was prepared using a similar procedure as described in Example 1, except using 2-chloro-3,4-dihydroxybenzohydrazide instead of 2-chloro-4,5-dihydroxybenzohydrazide. 1H NMR (400MHz, DMSO-d6)δ 12.12(s,H), 10.21(s,1H), 9.43(s,1H), 7.84(s,1H), 7.13(d,1H), 6.89(d,1H), 6.60(s,1H), 5.33( d,1H), 5.04(s,1H), 3.75(t,1H), 3.36(m,1H), 2.23(s,1H), 1.64(s,3H);LC-MS(ESI):m / z=432(M+H) +

[0119] Example 24 (2S,3R,5R)-3-((E)-(2-(3,6-difluoropicolinoyl)hydrazono)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0120] The title compound was prepared using a similar procedure as described in Example 1, except using 3,6-difluoropicolinohydrazide instead of 2-chloro-4,5-dihydroxybenzohydrazide. 1 H NMR (400MHz, DMSO-d6)δ 13.87(br,1H), 12.42(s,1H), 8.17(m,1H), 8.01(s,1H), 7.58(d,1H), 7.28(m,1H), 5.23( d,1H), 4.89(s,1H), 3.71(dd,1H), 3.33(dd,1H), 1.63(s,3H);LC-MS(ESI):m / z=368(M+H) +

[0121] Example 25 (2S,3R,5R)-3-((E)-(2-(3-(3,4-dihydroxyphenyl)propanoyl)hydrazono)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0122] The title compound was prepared using a similar procedure as described in Example 1, except 3-(3,4-dihydroxy-2-methylphenyl)propanehydrazide was used instead of 2-chloro-4,5-dihydroxybenzohydrazide. 1 H NMR (400MHz, DMSO-d6)δ 13.76(br,1H), 11.65(s,1H), 8.65(br,2H), 7.67(s,1H), 6.65(d,1H), 6.62(s,1H), 6.48(d,1H), 5.28(d,1H) , 4.90(s,1H), 3.72(d,1H), 3.31(dd,1H), 2.70(m,3H), 2.42(m,1H), 1.61(s,3H);LC-MS(ESI):m / z=426(M+H) +

[0123] Example 26 (2S,3R,5R)-3-((E)-(2-(2-(benzo[d][1,3]dioxol-5-yl)acetyl)hydrazono)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0124] The title compound was prepared using a similar procedure as described in Example 1, except using 2-(benzo[d][1,3]dioxol-5-yl)acetohydrazide instead of 2-chloro-4,5-dihydroxybenzohydrazide. 1 H NMR (400MHz, DMSO-d6)δ 13.76(br,1H), 9.92(s,1H), 9.35(s,1H), 6.67(s,1H), 6.63(d,1H), 6.84(s,1H), 5.97(s,2H), 5.13(d,1H), 4 .87(s,1H), 3.88(dd,1H), 3.35(s,2H), 3.26(dd,1H), 3.21(dd,1H), 1.61(s,3H);LC-MS(ESI):m / z=424(M+H) +

[0125] Example 27 (2S,3R,5R)-3-((E)-(2-(2,5-dihydroxy-3,6-dimethylbenzoyl)hydrazono)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0126] The title compound was prepared using a similar procedure as described in Example 1, except using 2,5-dihydroxy-3,6-dimethylbenzohydrazide instead of 2-chloro-4,5-dihydroxybenzohydrazide. 1 H NMR (400MHz, DMSO-d6)δ 9.64(s,1H), 8.98(s,1H), 7.50(s,1H), 6.97(s,1H), 6.68(s,1H), 5.24(s,1H), 4.70(t,1H), 3.46(m ,1H), 3.32(s,1H), 3.21(m,1H), 2.36(s,3H), 2.31(s,3H), 1.53(s,3H);LC-MS(ESI):m / z=426(M+H) +

[0127] Example 28 (2S,3R,5R)-3-((E)-(2-(2,3-dihydroxybenzoyl)hydrazono)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0128] The title compound was prepared using a similar procedure as described in Example 1, except using 2,3-dihydroxybenzohydrazide instead of 2-chloro-4,5-dihydroxybenzohydrazide. 1H NMR (400MHz, DMSO-d6)δ 12.12(s,H), 10.22(s,1H), 9.42(s,1H), 7.84(s,1H), 7.33(t,1H), 7.11(d,1H), 6.89(d,1H), 6.60( s,1H), 5.30(d,1H), 5.01(s,1H), 3.74(t,1H), 3.35(m,1H), 1.65(s,3H);LC-MS(ESI):m / z=398(M+H) +

[0129] Example 29 (2S,3R,5R)-3-((E)-(2-(4-hydroxybenzoyl)hydrazono)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0130] The title compound was prepared using a similar procedure as described in Example 1, except using 4-hydroxybenzohydrazide instead of 2-chloro-4,5-dihydroxybenzohydrazide. 1 H NMR (400MHz, DMSO-d6)δ 12.12(s,H), 10.20(s,1H), 9.40(s,1H), 7.83(m,2H), 7.11(s,1H), 6.91(m,2H), 6.60(m,1H), 5.33(d,1H), 5.02(s,1H), 3.74(t,1H), 3.34(m,1H), 1.65(s,3H);LC-MS(ESI):m / z=382(M+H) +

[0131] Example 30 (2S,3R,5R)-3-((E)-(2-(2-chloro-3,4-dimethoxybenzoyl)hydrazono)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0132] The title compound was prepared using a similar procedure as described in Example 1, except using 2-chloro-3,4-dimethoxybenzohydrazide instead of 2-chloro-4,5-dihydroxybenzohydrazide. 1 H NMR (400MHz, DMSO-d6)δ 12.12(s,H), 7.82(s,1H), 7.43(s,1H), 7.13(m,2H), 5.32(s,1H), 4.81(s,1H), 3.89(s ,3H), 3.85(s,3H), 3.74(m,1H), 3.34(m,1H), 1.64(s,3H);LC-MS(ESI):m / z=460(M+H) +

[0133] Example 31 (2S,3R,5R)-3-Methyl-3-((E)-(2-(4-methylbenzoyl)hydrazono)methyl)-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0134] The title compound was prepared using a similar procedure as described in Example 1, except using 4-methylbenzohydrazide instead of 2-chloro-4,5-dihydroxybenzohydrazide. 1 H NMR (400MHz, DMSO-d6)δ 12.13(s,1H), 7.94(s,1H), 7.81(d,2H), 7.34(d,2H), 5.31(d,1H), 4.91(s,1H), 3.76(dd,1H), 3.34(d,2H), 2.38(s,3H), 1.63(s,3H);LC-MS(ESI):m / z=380(M+H) +

[0135] Example 32 (2S,3R,5R)-3-Methyl-7-oxo-3-((E)-(2-(4-(trifluoromethyl)benzoyl)hydrazono)methyl)-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0136] The title compound was prepared using a similar procedure as described in Example 1, except using 4-(trifluoromethyl)benzohydrazide instead of 2-chloro-4,5-dihydroxybenzohydrazide. 1 H NMR (400MHz, DMSO-d6)δ 12.40(s,1H), 8.11(d,2H), 7.96(s,1H), 7.93(d,2H), 5.32(d,1H), 4.97(s ,1H), 3.76(dd,1H), 3.34(d,2H), 1.64(s,3H);LC-MS(ESI):m / z=434(M+H) +

[0137] Example 33 (2S,3R,5R)-3-((E)-(2-(4-fluorobenzoyl)hydrazono)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0138] The title compound was prepared using a similar procedure as described in Example 1, except using 4-fluorobenzohydrazide instead of 2-chloro-4,5-dihydroxybenzohydrazide. 1 H NMR (400MHz, DMSO-d6)δ 12.2(s,1H), 7.97(t,3H), 7.38(m,2H), 5.3(d,1H), 4.92(s,1H), 3.91(dd,1H), 3.33(d,2H), 1.63(s,3H);LC-MS(ESI):m / z=384(M+H) +

[0139] Example 34 (2S,3R,5R)-3-((E)-(2-benzoylhydrazono)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0140] The title compound was prepared using a similar procedure as described in Example 1, except using benzohydrazide instead of 2-chloro-4,5-dihydroxybenzohydrazide. 1 H NMR (400MHz, DMSO-d6)δ 12.22(s,1H), 7.95(s,1H), 7.90(d,2H), 7.61(d,1H), 7.55(m,2H), 5.32(d,1H), 4.94(s,1H), 3.77(dd,1H), 3.34(d,2H), 1.64(s,3H);LC-MS(ESI):m / z=366(M+H) +

[0141] Example 35 (2S,3R,5R)-3-((E)-(2-(4-methoxybenzoyl)hydrazono)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0142] The title compound was prepared using a similar procedure as described in Example 1, except using 4-methoxybenzohydrazide instead of 2-chloro-4,5-dihydroxybenzohydrazide. 1H NMR (400MHz, DMSO-d6)δ 12.07(s,1H), 7.93(m,3H), 7.06(d,2H), 5.31(d,1H), 4.91(s,1H), 3.83(s ,3H), 3.76(dd,1H), 3.34(d,2H), 1.62(s,3H);LC-MS(ESI):m / z=396(M+H) +

[0143] Example 36 (2S,3R,5R)-3-((E)-(2-(4-chlorobenzoyl)hydrazono)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0144] The title compound was prepared using a similar procedure as described in Example 1, except using 4-chlorobenzohydrazide instead of 2-chloro-4,5-dihydroxybenzohydrazide. 1 H NMR (400MHz, DMSO-d6)δ 12.25(s,1H), 7.95(m,3H), 7.61(d,2H), 5.3(d,1H), 4.93(s,1H), 3.76(dd,1H), 3.33(d,2H), 1.63(s,3H);LC-MS(ESI):m / z=400(M+H) +

[0145] Example 37 (2S,3R,5R)-3-((E)-(2-(3-ethyl-7-oxo-4,7-dihydropyrazolo[1,5-a]pyrimidine-5-carbonyl)hydrazono)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0146] The title compound was prepared using a procedure similar to that described in Example 1, except that 3-ethyl-7-oxo-4,7-dihydropyrazolo[1,5-a]pyrimidine-5-carbohydrazide was used instead of 2-chloro-4,5-dihydroxybenzohydrazide. 1 H NMR (400MHz, DMSO-d6)δ 13.86(br,1H), 12.58(s,1H), 7.98(s,1H), 7.90(s,1H), 6.25(s,1H), 5.16(d,1H), 4.57(s,1H), 3.61(dd,1H), 3.26(dd,1H), 2.69(q,2H), 1.64(s,3H), 1.20(t,3H);LC-MS(ESI):m / z=451(M+H) +

[0147] Example 38 (2S,3R,5R)-3-((E)-(2-(1-(2-chloro-3,4-dihydroxybenzoyl)pyrrolidine-3-carbonyl)hydrazono)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0148] FIG. 6 shows a synthetic scheme for preparing this compound. Step 1. Methyl 1-(2-chloro-3,4-bis((4-methoxybenzyl)oxy)benzoyl)pyrrolidine-3-carboxylate 2-Chloro-3,4-bis((4-methoxybenzyl)oxy)benzoic acid (1 g, 2.3 mmol) and methyl pyrrolidine-3-carboxylate (0.3 g, 2.3 mmol) were dissolved in 10 mL of DMF in a round-bottom flask. EDCI (0.7 g, 4.6 mmol), HOBT (0.3 g, 2.3 mmol) and then NMM (0.7 g, 6.9 mmol) were added to the flask. The mixture was stirred at room temperature for 6 hours. The solvent was then poured into ice water to give a white solid, and the crude product was filtered and dried under vacuum (1.0 g, 81% yield); LC-MS (ESI): m / z=540 (M+H).+

[0149] Step 2. 1-(2-chloro-3,4-bis((4-methoxybenzyl)oxy)benzoyl)pyrrolidine-3-carbohydrazide Methyl 1-(2-chloro-3,4-bis((4-methoxybenzyl)oxy)benzoyl)pyrrolidine-3-carboxylate (1.0 g, 1.8 mmol) was dissolved in 30 mL of EtOH. Hydrazine hydrate (0.5 g, 9.3 mmol) was added and the solution was refluxed for 8 hours. The reaction solution was then cooled to room temperature. The white solid was filtered and dried as the crude product (0.7 g, 76% yield); LC-MS (ESI): m / z=540 (M+H). +

[0150] Step 3. (2S,3R,5R)-Benzhydryl 3-((E)-(2-(1-(2-chloro-3,4-bis((4-methoxybenzyl)oxy)benzoyl)pyrrolidine-3-carbonyl)hydrazono)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate 4,4-dioxide (2S,5R)-Benzhydryl 3-formyl-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate 4,4-dioxide (0.6 g, 1.3 mmol) and 1-(2-chloro-3,4-bis((4-methoxybenzyl)oxy)benzoyl)pyrrolidine-3-carbohydrazide (0.7 g, 1.3 mmol) were dissolved in 20 mL of DMF and the solution was stirred at room temperature for 8 hours. The solvent was then evaporated under vacuum and the residue was purified on silica gel (ethyl acetate:petroleum ether=1:1) to give a white solid (0.7 g, 51% yield). LC-MS (ESI): m / z=935 (M+H) +

[0151] Step 4: (2S,3R,5R)-3-((E)-(2-(1-(2-chloro-3,4-dihydroxybenzoyl)pyrrolidine-3-carbonyl)hydrazono)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide (2S,5R)-Benzhydryl 3-((E)-(2-(1-(2-chloro-3,4-bis((4-methoxybenzyl)oxy)benzoyl)pyrrolidine-3-carbonyl)hydrazono)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate 4,4-dioxide (0.7 g, 0.9 mmol) was dissolved in 30 mL of THF, Pd / C (10%, 100 mg) was added, and the solution was stirred under a hydrogen-charged balloon for 8 h. Palladium was removed by filtration. The solvent was then evaporated under vacuum, and the residue was purified by column chromatography (silica gel, DCM:MeOH=20:1) to give the title compound as a white solid (321 mg, 67% yield). 1 H NMR (400MHz, DMSO-d6)δ 8.31(s,1H), 7.50(s,1H), 7.17(d,1H), 6.66(d,1H), 5.43(s,1H), 4.70(t,1H), 4.46(s,1H), 4.27(s,1H), 3.89(m,1H), 3.71(m,1H), 3.64(m,1H), 3.55(m,1H), 3.46(m,1H), 3.21(m,1H), 2.95(m,1H), 2.19(m,1H), 1.6(s,3H), 1.91(m,1H);LC-MS(ESI):m / z=529(M+H) +

[0152] Example 39 (2S,3R,5R)-3-((E)-(2-(1-(2-chloro-3,4-dihydroxybenzoyl)azetidine-3-carbonyl)hydrazono)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0153] The title compound was prepared using a similar procedure as described in Example 38, except using methyl azetidine-3-carboxylate instead of methyl pyrrolidine-3-carboxylate. 1 H NMR (400MHz, DMSO-d6)δ 8.97(s,1H), 7.11(s,1H), 6.80(s,1H), 6.22(s,1H), 5.16(s,1H), 5.02(s,1H), 4.31(t,1H), 3.85-3.79(m,2H), 3.59-3.54(m,2H), 3.19(m,1H), 3.07(m,1H), 2.89(s,1H), 2.82(m,1H), 1.62(m,3H);LC-MS(ESI):m / z=515(M+H) +

[0154] Example 40 (2S,3R,5R)-3-((E)-(2-(1-(2-chloro-3,4-dihydroxybenzoyl)pyrrolidine-2-carbonyl)hydrazono)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0155] The title compound was prepared using a similar procedure as described in Example 38, except using methyl pyrrolidine-2-carboxylate instead of methyl pyrrolidine-3-carboxylate. 1 H NMR (400MHz, DMSO-d6)δ 9.66(s,1H), 7.50(s,1H), 7.03(d,1H), 6.62(d,1H), 5.15(s,1H), 5.08(s,1H), 4.70(t,1H), 3.83(m,1H), 3.47(m,2H), 3.21(m,1H), 2.92(m,1H), 2.83(m,1H), 2.18(m,1H), 1.93(d,2H), 1.86(s,1H), 1.50(s,3H);LC-MS(ESI):m / z=529(M+H) +

[0156] Example 41 (2S,3R,5R)-3-((E)-(2-(5-(3,4-dihydroxybenzamido)picolinoyl)hydrazono)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0157] The title compound was prepared using a procedure similar to that described in Example 38. 1 H NMR (400MHz, DMSO-d6)δ 13.81(br,1H), 12.43(s,1H), 10.48(s,1H), 9.79(s,1H), 9.34(s,1H), 9.08(d,1H), 8.44(dd,1H), 8.14(s,1H), 8.11(d,1H), 7.44( dd,1H), 7.42(dd,1H), 6.87(d,1H), 5.32(d,1H), 4.81(s,1H), 3.78(dd,1H), 3.26(dd,1H), 1.63(s,3H);LC-MS(ESI):m / z=518(M+H) +

[0158] Example 42 (2S,3R,5R)-3-((E)-(2-(1-(2-chloro-3,4-dihydroxybenzoyl)piperidine-4-carbonyl)hydrazono)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0159] The title compound was prepared using a similar procedure as described in Example 38, except using methyl piperidine-4-carboxylate instead of methyl pyrrolidine-3-carboxylate. 1H NMR (400MHz, DMSO)δ 8.28(s,1H), 7.50(s,1H), 7.19(d,1H), 6.66(d,1H), 5.43(s,1H), 4.70(t,1H), 4.47(s,1H), 4.26(s,1H), 3.72-3.68( m,2H), 3.44(m,4H), 3.21(m,4H), 2.53(s,1H), 2.07(m,2H), 1.88-1.84(m,2H), 1.6(s,3H);LC-MS(ESI):m / z=543(M+H) +

[0160] Example 43 (2S,3R,5R)-3-((E)-(2-(2-(2-chloro-3,4-dihydroxybenzamido)-3-hydroxypropanoyl)hydrazono)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0161] The title compound was prepared using a similar procedure as described in Example 38, except using (S)-methyl 2-amino-3-hydroxypropanoate instead of methyl pyrrolidine-3-carboxylate. 1 H NMR (400MHz, DMSO-d6)δ 9.77(s,1H), 7.50(s,1H), 7.40(s,1H), 7.22(d,1H), 6.67(d,1H), 6.60(s,1H), 5.54(s,1H), 4.70(t,1H), 4.53(s ,1H), 4.28(m,2H), 4.11(m,1H), 3.81(m,1H), 3.46(m,1H), 3.21(m,1H), 1.70(s,3H);LC-MS(ESI):m / z=519(M+H) +

[0162] Example 44 (2S,3R,5R)-3-((E)-(2-(2-(2-chloro-3,4-dihydroxybenzamido)-3-phenylpropanoyl)hydrazono)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0163] The title compound was prepared using a similar procedure as described in Example 38, except using (S)-methyl 2-amino-3-phenylpropanoate instead of methyl pyrrolidine-3-carboxylate. 1 H NMR (400MHz, DMSO-d6)δ 7.01(s,1H), 6.84-6.76(m,3H), 6.76-6.65(m,3H), 6.62(s,1H), 6.13(d,1H), 4.97(s,1H), 4.62(t,1H), 4.21(t,1H), 4 .09(s,1H), 3.76(s,1H), 2.97(m,1H), 2.72(m,1H), 2.67(m,1H), 2.45(s,1H), 1.59(s,3H);LC-MS(ESI):m / z=579(M+H) +

[0164] Example 45 (2S,3R,5R)-3-((E)-(2-(4-((2-chloro-3,4-dihydroxybenzamido)methyl)benzoyl)hydrazono)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0165] The title compound was prepared using a similar procedure as described in Example 38, except using methyl 4-(aminomethyl)benzoate instead of methyl pyrrolidine-3-carboxylate. 1H NMR (400MHz, DMSO-d6)δ 9.80(s,1H), 7.64(s,1H), 7.50(s,1H), 7.29-7.25(m,2H), 7.17(s,1H), 6.77(m,1H), 5.54(s,1H), 4.70(t,1H), 4.42(t,1H) ), 4.28(s,1H), 4.03(m,1H), 3.80(m,1H), 3.57(s,1H), 3.46(s,1H), 3.21(s,1H), 1.74(s,3H);LC-MS(ESI):m / z=485(M+H) +

[0166] Example 46 (2S,3R,5R)-3-((E)-(2-(4-((3,4-dihydroxybenzamido)methyl)benzoyl)hydrazono)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0167] The title compound was prepared using a procedure similar to that described in Example 38, except for substituting methyl 4-(aminomethyl)benzoate for methyl pyrrolidine-3-carboxylate and 3,4-bis((4-methoxybenzyl)oxy)benzoic acid for 2-chloro-3,4-bis((4-methoxybenzyl)oxy)benzoic acid. 1 H NMR (400MHz, DMSO-d6)δ 9.86(s,1H), 8.86(s,1H), 7.95-7.80(m,2H), 7.52-7.41(m,3H), 7.30(m,1H), 7.19(s,1H), 6.73(d,1H), 6.36(s,1H), 5.05(s,1H) ), 4.70(t,1H), 4.61(s,1H), 4.53(s,1H), 3.87(s,1H), 3.51-3.44(m,2H), 3.21(m,1H), 1.53(s,3H);LC-MS(ESI):m / z=485(M+H) +

[0168] Example 47 ((2S,3R,5R)-3-((E)-(2-(2-(3,4-dihydroxybenzamido)-3-methylbutanoyl)hydrazono)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0169] The title compound was prepared using a procedure similar to that described in Example 38, except for the use of (S)-methyl 2-amino-3-methylbutanoate instead of methyl pyrrolidine-3-carboxylate and 3,4-bis((4-methoxybenzyl)oxy)benzoic acid instead of 2-chloro-3,4-bis((4-methoxybenzyl)oxy)benzoic acid. 1 H NMR (400MHz, DMSO-d6)δ 9.94(s,1H), 7.50(s,1H), 7.39(s,1H), 7.27(d,J=12.4Hz,2H), 6.78(s,1H), 5.60(s,1H), 4.70(s,1H), 4.56(s,1H), 4.26(s, 1H), 3.54(s,1H), 3.46(s,1H), 3.21(s,1H), 2.43(s,1H), 1.68(s,3H), 1.10(s,3H), 0.96(s,3H);LC-MS(ESI):m / z=497(M+H) +

[0170] Example 48 (2S,3R,5R)-3-((E)-(2-(2-(2-chloro-3,4-dihydroxybenzamido)-3-methylbutanoyl)hydrazono)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0171] The title compound was prepared using a similar procedure as described in Example 38, except using (S)-methyl 2-amino-3-methylbutanoate instead of methyl pyrrolidine-3-carboxylate. 1 H NMR (400MHz, DMSO-d6)δ 9.82(s,1H), 8.31(s,1H), 7.50(s,1H), 7.20(s,1H), 7.01(d,1H), 6.66(d,1H), 5.65(s,1H), 4.70(s,1H), 4.52(s,1H), 4.40(d ,1H), 4.27(s,1H), 3.46(m,1H), 3.21(m,1H), 2.48(m,1H), 1.76(s,3H), 1.11(s,3H), 0.97(s,3H);LC-MS(ESI):m / z=531(M+H) +

[0172] Example 49 (2S,3R,5R)-3-((E)-(2-(1-(2-chloro-3,4-dihydroxybenzoyl)piperidine-3-carbonyl)hydrazono)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0173] The title compound was prepared using a similar procedure as described in Example 38, except using methyl piperidine-3-carboxylate instead of methyl pyrrolidine-3-carboxylate. 1 H NMR (400MHz, DMSO-d6)δ 8.76(s,1H), 7.50(s,1H), 7.16(d,1H), 6.64(d,1H), 5.90(s,1H), 4.70(t,1H), 3.98(m,1H), 3.93(s,1H), 3.55-3.44(m,5H) ), 3.21(m,1H), 2.50(m,1H), 2.12(m,1H), 1.95(m,1H), 1.88(m,1H), 1.82(m,1H), 1.61(s,3H);LC-MS(ESI):m / z=543(M+H) +

[0174] Example 50 (2S,3R,5R)-3-((E)-(2-(2-(3,4-dihydroxybenzamido)-3-hydroxypropanoyl)hydrazono)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0175] The title compound was prepared using a procedure similar to that described in Example 38, except for the use of (S)-methyl 2-amino-3-phenylpropanoate instead of methyl pyrrolidine-3-carboxylate and 3,4-bis((4-methoxybenzyl)oxy)benzoic acid instead of 2-chloro-3,4-bis((4-methoxybenzyl)oxy)benzoic acid. 1 H NMR (400MHz, DMSO-d6)δ 9.80(s,1H), 7.64(s,1H), 7.50(s,1H), 7.29-7.25(m,2H), 7.17(s,1H), 6.77(m,1H), 5.54(s,1H), 4.70(t,1H), 4.42(t,1H) ), 4.28(s,1H), 4.03(m,1H), 3.80(m,1H), 3.57(s,1H), 3.46(s,1H), 3.21(s,1H), 1.74(s,3H);LC-MS(ESI):m / z=485(M+H) +

[0176] Example 51 (2S,3R,5R)-3-((E)-(2-(2-(3,4-dihydroxybenzamido)-3-phenylpropanoyl)hydrazono)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0177] The title compound was prepared using a procedure similar to that described in Example 38, except for the use of (S)-methyl 2-amino-3-phenylpropanoate instead of methyl pyrrolidine-3-carboxylate and 3,4-bis((4-methoxybenzyl)oxy)benzoic acid instead of 2-chloro-3,4-bis((4-methoxybenzyl)oxy)benzoic acid. 1 H NMR (400MHz, DMSO-d6)δ 9.49(s,1H), 7.09(s,1H), 6.92(d,1H), 6.88(m,4H), 6.76(s,1H), 6.74(d,2H), 6.30(d,1H), 5.35(s,1H), 5.20(s,1H), 4.39(t,1H), 4.29(t,1H), 3.79(s,1H), 3.06(s,1H), 3.00(m,1H), 2.83(m,2H), 2.78(m,1H), 2.61(m,1H), 1.56(s,3H);LC-MS(ESI):m / z=545(M+H) +

[0178] Example 52 (2S,3R,5R)-3-((E)-(2-(1-(3,4-dihydroxybenzamido)cyclopropanecarbonyl)hydrazono)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0179] The title compound was prepared using a procedure similar to that described in Example 38, except for using methyl 1-aminocyclopropanecarboxylate instead of methyl pyrrolidine-3-carboxylate and 3,4-bis((4-methoxybenzyl)oxy)benzoic acid instead of 2-chloro-3,4-bis((4-methoxybenzyl)oxy)benzoic acid. 1H NMR (400MHz, DMSO-d6)δ 9.81(s,1H), 7.50(s,1H), 7.22(d,2H), 6.73(d,2H), 5.58(s,1H), 4.70(t,1H), 4.22(s,1H), 3.46( m,2H), 3.21(m,1H), 1.68(s,3H), 0.99-0.94(m,2H), 0.74-0.69(m,2H)LC-MS(ESI): m / z=481(M+H) +

[0180] Example 53 (2S,3R,5R)-3-((E)-(2-(1-(2-chloro-3,4-dihydroxybenzamido)cyclopropanecarbonyl)hydrazono)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0181] The title compound was prepared using a similar procedure as described in Example 38, except using methyl 1-aminocyclopropanecarboxylate instead of methyl pyrrolidine-3-carboxylate. 1 H NMR (400MHz, DMSO-d6)δ 9.42(s,1H), 8.09(s,1H), 7.90(s,1H), 7.28(s,1H), 7.02(d,1H), 6.41(d,1H), 5.43(s,1H), 4.48(t,1H), 4.23(s ,1H), 3.29(s,1H), 3.24(m,1H), 2.99(m,1H), 1.77(s,3H), 0.75(m,2H), 0.50(m,2H);LC-MS(ESI):m / z=515(M+H) +

[0182] Example 54 (2S,3R,5R)-3-((E)-(2-(4-((3,4-dihydroxybenzoyl)oxy)benzoyl)hydrazono)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0183] The title compound was prepared using a similar procedure as described in Example 1, except using 4-(hydrazinecarbonyl)phenyl 3,4-bis(benzyloxy)benzoate instead of 2-chloro-4,5-dihydroxybenzohydrazide. 1 H NMR (400MHz, DMSO-d6)δ 9.20(s,1H), 7.98-7.84(m,2H), 7.58-7.47(m,3H), 7.35-7.21(m,2H), 6.75(d,1H), 5.76(s,1H), 4.70 (t,1H), 3.68(s,1H), 3.54(s,1H), 3.46(m,1H), 3.21(m,1H), 1.80(s,3H);LC-MS(ESI):m / z=518(M+H) +

[0184] Example 55 (2S,3R,5R)-3-((E)-(2-(2-((tert-butoxycarbonyl)amino)-3-((2-chloro-3,4-dihydroxybenzoyl)oxy)propanoyl)hydrazono)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0185] The title compound was prepared using a procedure similar to that described in Example 1, except that 2-((tert-butoxycarbonyl)amino)-3-hydrazinyl-3-oxopropyl 2-chloro-3,4-bis((4-methoxybenzyl)oxy)benzoate was used instead of 2-chloro-4,5-dihydroxybenzohydrazide. 1H NMR (400MHz, DMSO-d6)δ 7.34(s,1H), 7.04(d,1H), 6.44(d,1H), 5.36(s,1H), 5.28(s,1H), 5.02(t,1H), 4.89(m,1H), 4.67(m,1H), 4.54(t ,1H), 4.25(s,1H), 4.13(s,1H), 3.30(m,1H), 3.05(m,1H), 1.89(s,3H), 1.30(s,9H);LC-MS(ESI):m / z=619(M+H) +

[0186] Example 56 (2S,3R,5R)-3-((E)-(2-(3',4'-dihydroxy-[1,1'-biphenyl]-4-carbonyl)hydrazono)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0187] The title compound is 2-chloro-4,5-dihydroxybenzohydrazide. This was prepared using a procedure similar to that described in Example 1, except that 3',4'-dihydroxy-[1,1'-biphenyl]-4-carbohydrazide was used instead of

[0188] 1 H NMR (400MHz, DMSO-d6)δ 12.22(s,1H), 9.20(d,2H), 8.04(m,3H), 7.76(d,2H), 7.24(s,1H), 7.13(m,1H), 6.92(d,1H), 6.6 2(m,1H), 5.32(s,1H), 4.89(s,1H), 3.77(d,1H), 3.32(d,3H), 1.72(s,3H);LC-MS:m / z=474(M+H) +

[0189] Example 57 (2S,3R,5R)-3-((E)-(2-(4-((2-chloro-3,4-dihydroxybenzoyl)oxy)benzoyl)hydrazono)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0190] The title compound is 2-chloro-4,5-dihydroxybenzohydrazide. This was prepared using a procedure similar to that described in Example 1, except using 4-(hydrazinecarbonyl)phenyl 3,4-bis(benzyloxy)-2-chlorobenzoate instead of 1 H NMR (400MHz, DMSO-d6)δ 7.70-7.56(m,2H), 7.20(s,1H), 7.17-7.02(m,3H), 6.32(d,1H), 5.11(s,1H), 4.40(t,1H), 4 .07(s,1H), 3.88(s,1H), 3.16(m,1H), 2.91(m,1H), 1.66(s,3H);LC-MS(ESI):m / z=552(M+H) +

[0191] Example 58 (2S,3R,5R)-3-((E)-(2-(5-(2-chloro-3,4-dihydroxybenzamido)picolinoyl)hydrazono)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0192] The title compound was prepared using a procedure similar to that described in Example 38. 1H NMR (400MHz, DMSO-d6):δ 13.81(br,1H), 12.42(s,1H), 10.81(s,1H), 10.23(s,1H), 9.44(s,1H), 9.00(s,1H), 8.38(d,1H), 8.15(s,1H), 8.11(d,1H) , 6.98(d,1H), 6.85(d,1H), 5.32(d,1H), 4.81(s,1H), 3.78(dd,1H), 3.26(dd,1H), 1.63(s,3H);LC-MS(ESI):m / z=552(M+H) +

[0193] Example 59 (2S,3R,5R)-3-((E)-(2-(2-(2-chloro-3,4-dihydroxybenzamido)acetyl)hydrazono)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0194] FIG. 7 shows a synthetic scheme for preparing this compound. Step 1: Methyl 2-(2-chloro-3,4-bis((4-methoxybenzyl)oxy)benzamide)acetate To a solution of 2-chloro-3,4-bis((4-methoxybenzyl)oxy)benzoic acid (2.2 g, 5.1 mmol) in DMF (40 mL) was added methyl 2-aminoacetate hydrochloride (0.63 g, 5.0 mmol), EDCI (1.9 g, 10 mmol), HOBT (0.7 g, 5.0 mmol) followed by NMM (0.5 g, 5.0 mmol). The mixture was stirred at room temperature for 6 h. The solution was then poured into ice water. The mixture was stirred for 0.5 h and filtered under reduced pressure. The filter cake was collected and dried by lyophilization to give the title compound as a pale solid (2.3 g, 90% yield); LC-MS (ESI): m / z=500 (M+H). +

[0195] Step 2: 2-chloro-N-(2-hydrazinyl-2-oxoethyl)-3,4-bis((4-methoxybenzyl)oxy)benzamide To a solution of methyl 2-(2-chloro-3,4-bis((4-methoxybenzyl)oxy)benzamido)acetate (2.0 g, 4.0 mmol) in EtOH (50 mL) was added hydrazine hydrate (85% in water, 3.0 g, 51 mmol). The mixture was stirred at 80° C. for 16 h. The temperature was allowed to cool to room temperature. A lot of solid precipitated. The mixture was filtered under reduced pressure. The filter cake was collected and dried under vacuum to give a white solid (2 g, 100% yield); LC-MS (ESI): m / z=500 (M+H). +

[0196] Step 3: 2-Chloro-N-(2-hydrazinyl-2-oxoethyl)-3,4-dihydroxybenzamide hydrochloride A solution of 2-chloro-N-(2-hydrazinyl-2-oxoethyl)-3,4-bis((4-methoxybenzyl)oxy)benzamide (1.0 g, 2.0 mmol) in HCl / EtOH (10 mL, 4.0 M) was stirred at room temperature for 5 h. The solvent was evaporated under vacuum. The crude (600 mg) was used in the next step without further purification. LC-MS: m / z=260 (M+H). +

[0197] Step 4: (2S,3R,5R)-Benzhydryl 3-((E)-(2-(2-(2-chloro-3,4-dihydroxybenzamido)acetyl)hydrazono)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate 4,4-dioxide To a solution of 2-chloro-N-(2-hydrazinyl-2-oxoethyl)-3,4-dihydroxybenzamide hydrochloride (1.0 g, 3.4 mmol) in EtOH / DCM (10 / 10 mL) was added (2S,3R,5R)-benzhydryl 3-formyl-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate 4,4-dioxide (1.5 g, 3.6 mmol) and pyridine (0.1 g, 1.3 mmol). The solution was stirred at room temperature for 3 hours. The solvent was evaporated under vacuum. The residue was purified by column chromatography (silica gel, DCM:MeOH=20:1) to give the title compound as a white solid (400 mg, 18% yield); LC-MS (ESI): m / z=655 (M+H). +

[0198] Step 5: (2S,3R,5R)-3-((E)-(2-(2-(2-chloro-3,4-dihydroxybenzamido)acetyl)hydrazono)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide A solution of (2S,3R,5R)-benzhydryl 3-((E)-(2-(2-(2-chloro-3,4-dihydroxybenzamido)acetyl)hydrazono)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate 4,4-dioxide (400 mg, 0.6 mmol) in m-cresol (5 mL) was stirred at 50° C. for 5 hours. The solution was poured into PE (10 mL). The solid obtained by filtration was purified by column chromatography (silica gel, DCM:MeOH=20:1) to give the title compound as a white solid (90 mg, 30% yield). 1H NMR (400MHz, DMSO-d6)δ 11.86(s,1H), 9.50(s,1H), 9.23(s,1H), 7.33(s,1H), 7.04(d,1H), 6.82(d,1H), 6.65(m,2H), 5.33(s,1H), 5.00(s,1H), 4.22(d,1H), 3.72(d,1H), 3.62(s,1H), 2.20(s,2H), 1.61(s,3H);LC-MS(ESI):m / z=489(M+H) +

[0199] Example 60 (2S,3R,5R)-3-((E)-(2-(3-(2-chloro-3,4-dihydroxybenzamido)propanoyl)hydrazono)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0200] The title compound was prepared using a similar procedure as described in Example 59, except using methyl 3-aminopropanoate·hydrochloride instead of methyl 2-aminoacetate·hydrochloride. 1 H NMR (400MHz, DMSO-d6)δ 11.85(s,1H), 9.50(s,1H), 9.31(s,1H), 8.22(s,1H), 7.02(d,1H), 6.63(m,2H), 5.32(s,1H), 5.04( s,1H), 3.84(d,1H), 3.53(m,2H), 3.33(d,1H), 2.20(m,2H), 1.62(s,3H);LC-MS(ESI):m / z=503(M+H) +

[0201] Example 61 (2S,3R,5R)-3-((E)-(2-(6-(2-chloro-3,4-dihydroxybenzamido)hexanoyl)hydrazono)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0202] The title compound was prepared using a similar procedure as described in Example 59, except using methyl 6-aminohexanoate·hydrochloride instead of methyl 3-aminopropanoate·hydrochloride. 1 H NMR (400MHz, DMSO-d6)δ 11.85(s,1H), 9.54(s,1H), 9.34(s,1H), 8.13(s,1H), 7.56(s,1H), 6.74(d,2H), 6.56(s,1H), 5.34(s,1H), 5.05(s,1H), 3.83(d,1H), 3.23(m,3H), 2.20(m,2H), 1.60(s,3H), 1.44(m,6H);LC-MS(ESI):m / z=545(M+H) +

[0203] Example 62 (2S,3R,5R)-3-((E)-(2-((S)-2-(2-chloro-3,4-dihydroxybenzamido)propanoyl)hydrazono)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0204] The title compound was prepared using a similar procedure as described in Example 59, except using (S)-methyl 2-aminopropanoate·hydrochloride instead of methyl 2-aminoacetate·hydrochloride. 1H NMR (400MHz, DMSO-d6)δ 11.85(s,1H), 9.55(s,1H), 9.22(s,1H), 7.33(s,1H), 7.02(d,1H), 6.85(s,1H), 6.64(d,1H), 5.33(s,1H), 5.03( s,1H), 4.23(d,1H), 3.73(d,1H), 3.66(s,1H), 2.23(m,1H), 1.60(s,3H), 1.44(d,3H);LC-MS(ESI):m / z=503(M+H) +

[0205] Example 63 (2S,3R,5R)-3-((E)-(2-(4-(2-chloro-3,4-dihydroxybenzamido)butanoyl)hydrazono)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0206] The title compound was prepared using a similar procedure as described in Example 59, except using methyl 4-aminobutanoate hydrochloride instead of (S)-methyl 2-aminopropanoate hydrochloride. 1 H NMR (400MHz, DMSO-d6)δ 11.84(s,1H), 9.54(s,1H), 9.32(s,1H), 8.23(s,1H), 7.33(s,1H), 6.82(s,1H), 6.61(m,2H), 5.32(s,1H), 5.01(s ,1H), 3.85(d,1H), 3.34(m,1H), 2.54(m,2H), 2.20(m,2H), 1.82(br,2H), 1.60(s,3H);LC-MS(ESI):m / z=517(M+H) +

[0207] Example 64 (2S,3R,5R)-3-((E)-(2-(2-(3,4-dihydroxybenzamido)acetyl)hydrazono)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0208] FIG. 9 shows a synthetic scheme for preparing this compound. Step 1: Methyl 2-(3,4-bis((4-methoxybenzyl)oxy)benzamido)acetate To a solution of 3,4-bis((4-methoxybenzyl)oxy)benzoic acid (2.0 g, 5.1 mmol) in DMF (40 mL) was added methyl 2-aminoacetate hydrochloride (0.63 g, 5.0 mmol), EDCI (1.9 g, 10 mmol), HOBT (0.7 g, 5.0 mmol) followed by NMM (0.5 g, 5.0 mmol). The mixture was stirred at room temperature for 6 h. The solution was then poured into ice water. The mixture was stirred for 0.5 h and filtered under reduced pressure. The filter cake was collected and dried by lyophilization to give the title compound as a pale solid (2.3 g, 97% yield); LC-MS (ESI): m / z=466 (M+H). +

[0209] Step 2: N-(2-hydrazinyl-2-oxoethyl)-3,4-bis((4-methoxybenzyl)oxy)benzamide To a solution of methyl 2-(3,4-bis((4-methoxybenzyl)oxy)benzamido)acetate (2.3 g, 5.0 mmol) in EtOH (50 mL) was added hydrazine hydrate (85% in water, 3.0 g, 51 mmol). The mixture was stirred at 80° C. for 16 h. The temperature was allowed to cool to room temperature. A lot of solid precipitated. The system was filtered under reduced pressure. The filter cake was collected and dried under vacuum to give a white solid (2.3 g, 100% yield); LC-MS (ESI): m / z=466 (M+H). +

[0210] Step 3: N-(2-hydrazinyl-2-oxoethyl)-3,4-dihydroxybenzamide A solution of N-(2-hydrazinyl-2-oxoethyl)-3,4-bis((4-methoxybenzyl)oxy)benzamide (0.96 g, 2.0 mmol) in HCl / EtOH (10 mL, 4.0 M) was stirred at room temperature for 5 h. The solvent was evaporated under vacuum. The residue was used in the next step without further purification (600 mg); LC-MS (ESI): m / z=226 (M+H). +

[0211] Step 4: (2S,3R,5R)-Benzhydryl 3-((E)-(2-(2-(3,4-dihydroxybenzamido)acetyl)hydrazono)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate 4,4-dioxide To a solution of N-(2-hydrazinyl-2-oxoethyl)-3,4-dihydroxybenzamide (1.0 g, 3.8 mmol) in EtOH / DCM (10 / 10 mL), (2S,3R,5R)-benzhydryl 3-formyl-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate 4,4-dioxide (1.5 g, 3.6 mmol) and pyridine (0.1 g, 1.3 mmol) were added. The solution was stirred at room temperature for 3 hours. The solvent was evaporated under vacuum. The residue was purified by column chromatography (silica gel, DCM:MeOH=20:1) to give the title compound as a white solid (400 mg, 18% yield); LC-MS (ESI): m / z=621 (M+H). +

[0212] Step 5: (2S,3R,5R)-3-((E)-(2-(2-(3,4-dihydroxybenzamido)acetyl)hydrazono)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide A solution of (E)-benzhydryl 3-((2-(2-(3,4-dihydroxybenzamido)acetyl)hydrazono)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate 4,4-dioxide (400 mg, 0.6 mmol) in m-cresol (5 mL) was stirred at 50° C. for 5 hours. The solution was poured into PE (10 mL). The solid obtained by filtration was purified by silica gel column (DCM:MeOH=20:1) to obtain a white solid (90 mg, 30% yield). 1 H NMR (400MHz, DMSO-d6)δ 11.84(s,1H), 9.54(d,1H), 9.24(d,1H), 8.33(s,1H), 7.44(s,1H), 7.14(d,1H), 6.81(s,1H), 6.62(m,2H), 5.30( s,1H), 5.03(s,1H), 4.23(d,1H), 3.70(d,1H), 3.62(s,1H), 2.20(s,2H), 1.60(s,3H);LC-MS(ESI):m / z=455(M+H) +

[0213] Example 65 (2S,3R,5R)-3-((E)-(2-((S)-2-(3,4-dihydroxybenzamido)propanoyl)hydrazono)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0214] The title compound was prepared using a similar procedure as described in Example 64, except using (S)-methyl 2-aminopropanoate·hydrochloride instead of methyl 4-aminobutanoate·hydrochloride. 1H NMR (400MHz, DMSO-d6)δ 11.78(s,1H), 9.45(s,1H), 9.24(s,1H), 8.25(s,1H), 7.33(s,1H), 7.03(d,1H), 6.82(s,1H), 6.64(d,1H), 5.34(s,1H), 5.01(s,1H), 4.23(d,1H), 3.73(d,1H), 3.63(s,1H), 2.20(m,1H), 1.60(s,3H), 1.44(d,3H);LC-MS(ESI):m / z=469(M+H) +

[0215] Example 66 (2S,3R,5R)-3-((E)-(2-(4-(3,4-dihydroxybenzamido)butanoyl)hydrazono)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0216] The title compound was prepared using a similar procedure as described in Example 64, except using methyl 4-aminobutanoate hydrochloride instead of (S)-methyl 2-aminopropanoate hydrochloride.

[0217] 1 H NMR (400MHz, DMSO-d6)δ 11.80(s,1H), 9.51(s,1H), 9.32(s,1H), 8.21(s,1H), 7.64(s,1H), 7.35(s,1H), 6.86(s,1H), 6.65(m,2H), 5.33(s,1H), 5.07(s,1H), 3.84(d,1H), 3.34(m,1H), 2.50(m,2H), 2.20(m,2H), 1.82(br,2H), 1.61(s,3H);LC-MS(ESI):m / z=483(M+H) +

[0218] Example 67 (2S,3R,5R)-3-((E)-(2-(3-(3,4-dihydroxybenzamido)propanoyl)hydrazono)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0219] The title compound was prepared using a similar procedure as described in Example 64, except using methyl 3-aminopropanoate·hydrochloride instead of methyl 4-aminobutanoate·hydrochloride.

[0220] 1 H NMR (400MHz, DMSO-d6)δ 11.82(s,1H), 9.51(s,1H), 9.32(s,1H), 8.23(s,1H), 7.54(s,1H), 7.03(d,1H), 6.85(d,1H), 6.67(m,2H), 5.35( s,1H), 5.03(s,1H), 3.82(d,1H), 3.52(m,2H), 3.34(d,1H), 2.21(m,2H), 1.60(s,3H);LC-MS(ESI):m / z=469(M+H) +

[0221] Example 68 (2S,3R,5R)-3-((E)-(2-(6-(3,4-dihydroxybenzamido)hexanoyl)hydrazono)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0222] The title compound was prepared using a similar procedure as described in Example 64, except using methyl 6-aminohexanoate·hydrochloride instead of methyl 3-aminopropanoate·hydrochloride. 1H NMR (400MHz, DMSO-d6)δ 11.82(s,1H), 9.54(s,1H), 9.32(s,1H), 8.22(s,1H), 7.63(s,1H), 7.33(s,1H), 6.85(s,1H), 6.62(m,2H), 5.35( s,1H), 5.07(s,1H), 3.82(d,1H), 3.24(m,3H), 2.22(m,2H), 1.60(s,3H), 1.43(m,6H);LC-MS(ESI):m / z=511(M+H) +

[0223] Example 69 (2S,3R,5R)-3-(((2-(3,4-dihydroxybenzoyl)hydrazinecarbonyl)oxy)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0224] FIG. 9 shows a synthetic scheme for preparing this compound. Step 1: (2S,3R,5R)-Benzhydryl 3-methyl-3-((((4-nitrophenoxy)carbonyl)oxy)methyl)-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate 4,4-dioxide. (2S,3R,5R)-Benzhydryl 3-(hydroxymethyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate 4,4-dioxide (54 g, 0.13 mol) was dissolved in tetrahydrofuran (500 mL). The solution was cooled to 0° C. and 4-nitrophenyl carbonochloridate (52.4 g, 0.26 mol) was added. Pyridine (20 mL) and N,N-dimethylpyridin-4-amine (800 mg, 0.0065 mol) were then added. The mixture was stirred for 15 h. The solution was washed with water and extracted twice with ethyl acetate (200 mL). The organic layer was dried over Na2SO4. The solvent was evaporated under vacuum. The residue was purified by column chromatography (silica gel, DCM:Hexene=3:1) to give the title compound (29.4 g, 39.2% yield).

[0225] Step 2: (2S,3R)-Benzhydryl 3-(((2-(3,4-dihydroxybenzoyl)hydrazinecarbonyl)oxy)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate 4,4-dioxide To a solution of 3,4-dihydroxybenzohydrazide (0.4 g, 2.38 mmol) in DMF (5 mL) and pyridine (1 mL) was added (2S,3R)-benzhydryl 3-methyl-3-((((4-nitrophenoxy)carbonyl)oxy)methyl)-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate 4,4-dioxide (1.38 g, 2.38 mmol). The mixture was stirred at room temperature for 12 hours. The solution was washed with water and extracted with ethyl acetate (100 mL). The organic layer was dried over Na2SO4. The solvent was evaporated under vacuum. The residue was purified by column chromatography (silica gel, DCM:MeOH=100:1 to 50:1) to give the title compound (350 mg, 24% yield); LC-MS (ESI): m / z=610 (M+H). +

[0226] Step 3: (2S,3R)-3-(((2-(3,4-dihydroxybenzoyl)hydrazinecarbonyl)oxy)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide (2S,3R)-Benzhydryl 3-(((2-(3,4-dihydroxybenzoyl)hydrazinecarbonyl)oxy)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate 4,4-dioxide (350 mg, 0.57 mmol) was dissolved in THF (5 mL). The mixture was degassed twice with N2, Pd / C (10%, 150 mg) was added, then the flask was degassed twice with H2 and stirred at room temperature for 12 h. The solution was filtered and the filtrate was concentrated. Ethyl acetate (10 mL) was added and stirred for 30 min. The slurry was filtered and the cake was washed with MTBE (20 mL) to give the title compound (110 mg, 43% yield). 1H NMR (400MHz, DMSO-d6)δ 11.88(s,1H), 10.53(s,1H), 9.63(s,1H), 9.33(s,1H), 7.28(d,1H), 6.96(d,1H), 6.72(m,1H), 5.75(s,1H) , 5.16(s,1H), 4.68(d,1H), 4.51(d,1H), 3.66(d,1H), 3.26(d,1H), 1.51(s,3H);LC-MS(ESI):m / z=444(M+H) +

[0227] Example 70 (2S,3R,5R)-3-(((2-(2-chloro-3,4-dihydroxybenzoyl)hydrazinecarbonyl)oxy)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0228] The title compound was prepared using a similar procedure as described in Example 69, except using 2-chloro-3,4-dihydroxybenzohydrazide instead of 3,4-dihydroxybenzohydrazide. 1 H NMR (400MHz, DMSO-d6)δ 10.08(s,1H), 9.94(s,1H), 9.50(s,1H), 9.26(s,1H), 6.78(dd,2H), 5.75(s,1H), 5.16(d,1H), 4.68( d,1H), 4.57(s,1H), 4.54(d,1H), 3.61(dd,1H), 3.26(d,1H), 1.51(s,3H);LC-MS(ESI):m / z=478(M+H) +

[0229] Example 71 (2S,3R,5R)-3-(((2-(2-(3,4-dihydroxyphenyl)acetyl)hydrazinecarbonyl)oxy)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0230] The title compound was prepared using a similar procedure as described in Example 69, except using 2-(3,4-dihydroxyphenyl)acetohydrazide instead of 3,4-dihydroxybenzohydrazide. 1 H NMR (400MHz, DMSO-d6):δ 13.83(br,1H), 9.84(s,1H), 9.31(s,1H), 8.78(s,1H), 8.68(d,1H), 6.70(s,1H), 6.63(d,1H), 6.51(d,1H), 5.13(d,1H), 4.87(s,1H), 4.47(s,1H), 4.44(d,1H), 3.88(dd,1H), 3.26(dd,1H), 3.21(2, 1H), 1.48(s,3H);LC-MS(ESI):m / z=458(M+H) +

[0231] Example 72 (2S,3R,5R)-3-(((2-(2,3-dihydroxybenzoyl)hydrazinecarbonyl)oxy)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0232] The title compound was prepared using a similar procedure as described in Example 69, except using 2,3-dihydroxybenzohydrazide instead of 3,4-dihydroxybenzohydrazide. 1H NMR (400MHz, DMSO-d6)δ 11.88(s,1H), 10.53(s,1H), 9.64(s,1H), 9.34(s,1H), 7.28(d,1H), 6.96(d,1H), 6.73(t,1H), 5.75(s,1H), 5.16( d,1H), 4.68(d,1H), 4.57(s,1H), 4.54(d,1H), 3.61(dd,1H), 3.26(d,1H), 1.51(s,3H);LC-MS(ESI):m / z=444(M+H) +

[0233] Example 73 (2S,3R,5R)-3-Methyl-7-oxo-3-(((2-(3,4,5-trihydroxybenzoyl)hydrazinecarbonyl)oxy)methyl)-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0234] The title compound was prepared using a similar procedure as described in Example 69, except 3,4,5-trihydroxybenzohydrazide was used instead of 3,4-dihydroxybenzohydrazide. 1 H NMR (400MHz, DMSO-d6)δ 9.94(s,1H), 9.29(s,1H), 9.12(br,2H), 8.78(br,1H), 6.84(s,2H), 5.75(s,1H), 5.16(d,1H), 4.68( d,1H), 4.57(s,1H), 4.54(d,1H), 3.61(dd,1H), 3.26(d,1H), 1.51(s,3H);LC-MS(ESI):m / z=460(M+H) +

[0235] Example 74 (2S,3R,5R)-3-(((2-(2-hydroxy-3-methylbenzoyl)hydrazinecarbonyl)oxy)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0236] The title compound was prepared using a similar procedure as described in Example 69, except using 2-hydroxy-3-methylbenzohydrazide instead of 3,4-dihydroxybenzohydrazide. 1 H NMR (400MHz, DMSO-d6)δ 12.47(s,1H), 10.73(s,1H), 9.69(s,1H), 7.69(d,1H), 7.36(d,1H), 6.83(t,1H), 5.75(s,1H), 5.16(d,1H), 4.68(d ,1H), 4.57(s,1H), 4.54(d,1H), 3.61(dd,1H), 3.26(dd,1H), 2.18(s,3H), 1.51(s,3H);LC-MS(ESI):m / z=442(M+H) +

[0237] Example 75 (2S,3R,5R)-3-(((2-(4-hydroxybenzoyl)hydrazinecarbonyl)oxy)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0238] The title compound was prepared using a similar procedure as described in Example 69, except using 4-hydroxybenzohydrazide instead of 3,4-dihydroxybenzohydrazide. 1H NMR (400MHz, DMSO-d6): δ 13.81(br,1H), δ 13.84(br,1H), 10.11(br,2H), 9.38(s,1H), 7.75(d,2H), 6.84(d,1H), 6.63(d,1H), 6.51(d,1H), 5.13(d,1H), 4.87( s,1H), 4.47(s,1H), 4.44(d,1H), 3.88(dd,1H), 3.26(dd,1H), 3.21(2, 1H), 1.48(s,3H);LC-MS(ESI):m / z=428(M+H) +

[0239] Example 76 (2S,3R,5R)-3-(((2-(3,4-dihydroxybenzoyl)-1-methylhydrazinecarbonyl)oxy)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0240] The title compound was prepared using a similar procedure as described in Example 69, except using 3,4-dihydroxy-N'-methylbenzohydrazide instead of 3,4-dihydroxybenzohydrazide. 1 H NMR (400MHz, DMSO-d6)δ 13.82(br,1H), 10.51(s,1H), 9.64(s,1H), 9.27(s,1H), 7.28(d,2H), 6.79(d,1H), 5.16(d,1H), 4.68(d,1H), 4.57(s,1H), 4.54(d,1H), 3.61(dd,1H), 3.26(dd,1H), 3.13(s,3H), 1.51(s,3H);LC-MS(ESI):m / z=458(M+H) +

[0241] Example 77 (2S,3R,5R)-3-(((2-(2-chloro-4,5-dihydroxybenzoyl)hydrazinecarbonyl)oxy)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0242] The title compound was prepared using a similar procedure as described in Example 69, except 2-chloro-3,4-dihydroxy-N-methylbenzohydrazide was used instead of 3,4-dihydroxybenzohydrazide. 1 H NMR (400MHz, DMSO-d6)δ 13.84(br,1H), 10.08(s,1H), 9.86(s,1H), 9.61(s,1H), 6.65(d,1H), 6.55(d,1H), 5.16(d,1H), 4.68(d,1H), 4.57(s,1H), 4.54(d,1H), 3.61(dd,1H), 3.26(dd,1H), 3.10(s,3H), 1.51(s,3H);LC-MS(ESI):m / z=492(M+H) +

[0243] Example 78 (2S,3R,5R)-3-(((2-(2-hydroxybenzoyl)hydrazinecarbonyl)oxy)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0244] The title compound was prepared using a similar procedure as described in Example 69, except using 2-hydroxybenzohydrazide instead of 3,4-dihydroxybenzohydrazide. 1H NMR (400MHz, DMSO-d6)δ 13.84(br,1H), 11.96(s,1H), 10.49(s,1H), 9.62(s,1H), 7.84(d,1H), 7.45(d,1H), 6.95(dd,2H), 5.75(s,1H), 5.16 (d,1H), 4.68(d,1H), 4.57(s,1H), 4.54(d,1H), 3.61(dd,1H), 3.26(dd,1H), 1.51(s,3H);LC-MS(ESI):m / z=428(M+H) +

[0245] Example 79 (2S,3R,5R)-3-(((2-(3-ethyl-7-oxo-4,7-dihydropyrazolo[1,5-a]pyrimidine-5-carbonyl)hydrazinecarbonyl)oxy)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0246] The title compound was prepared using a similar procedure as described in Example 69, except 3-ethyl-7-oxo-4,7-dihydropyrazolo[1,5-a]pyrimidine-5-carbohydrazide was used instead of 3,4-dihydroxybenzohydrazide. 1 H NMR (400MHz, DMSO-d6)δ 13.81(br,1H), 10.81(s,1H), 9.73(s,1H), 7.85(s,1H), 6.18(s,1H), 5.75(s,1H), 5.16(d,1H), 4.68(d,1H), 4.57( s,1H), 4.54(d,1H), 3.61(dd,1H), 3.26(dd,1H), 2.69(q,2H), 1.51(s,3H), 1.17(t,3H);LC-MS(ESI):m / z=497(M+H) +

[0247] Example 80 (2S,3R,5R)-3-(((2-(2-chloro-3,4-dihydroxybenzoyl)-1-methylhydrazinecarbonyl)oxy)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0248] The title compound was prepared using a similar procedure as described in Example 69, except using 2-chloro-3,4-dihydroxy-N'-methylbenzohydrazide instead of 3,4-dihydroxybenzohydrazide. 1 H NMR (400MHz, DMSO-d6)δ 13.82(br,1H), 10.48(s,1H), 10.19(s,1H), 9.37(s,1H), 6.98(d,1H), 6.72(d,1H), 5.16(d,1H), 4.68(d,1H) , 4.57(s,1H), 4.54(d,1H), 3.61(dd,1H), 3.26(dd,1H), 3.08(s,3H), 1.51(s,3H);LC-MS(ESI):m / z=492(M+H) +

[0249] Example 81 (2S,3R,5R)-3-(((2-(3,4-dihydroxybenzoyl)-2-methylhydrazinecarbonyl)oxy)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0250] The title compound was prepared using a similar procedure as described in Example 69, except 3,4-dihydroxy-N-methylbenzohydrazide was used instead of 3,4-dihydroxybenzohydrazide. 1H NMR (400MHz, DMSO-d6)δ 13.82(br,1H), 10.10(s,1H), 9.34(s,1H), 9.10(s,1H), 6.91(s,1H), 6.82(d,1H), 6.68(d,1H), 5.16(d,1H), 4.68( d,1H), 4.57(s,1H), 4.54(d,1H), 3.61(dd,1H), 3.26(dd,1H), 3.07(s,3H), 1.51(s,3H);LC-MS(ESI):m / z=458(M+H) +

[0251] Example 82 (2S,3R,5R)-3-Methyl-7-oxo-3-(((2-(2,3,4-trihydroxybenzoyl)hydrazinecarbonyl)oxy)methyl)-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0252] The title compound was prepared using a similar procedure as described in Example 69, except using 2,3,4-trihydroxybenzohydrazide instead of 3,4-dihydroxybenzohydrazide. 1 H NMR (400MHz, DMSO-d6)δ 13.86(br,1H), 12.24(s,1H), 10.35(s,1H), 9.72(s,1H), 9.54(s,1H), 8.55(s,1H), 7.24(d,1H), 6.36(d,1H), 5.16( d,1H), 4.68(d,1H), 4.57(s,1H), 4.54(d,1H), 3.61(dd,1H), 3.26(dd,1H), 1.51(s,3H);LC-MS(ESI):m / z=460(M+H) +

[0253] Example 83 (2S,3R,5R)-3-(((2-(2,6-dichloro-3,4-dihydroxybenzoyl)hydrazinecarbonyl)oxy)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0254] The title compound was prepared using a similar procedure as described in Example 69, except using 2-chloro-4,5-dihydroxybenzohydrazide instead of 3,4-dihydroxybenzohydrazide. 1 H NMR (400MHz, DMSO-d6)δ 13.87(br,1H), 10.37(s,1H), 10.21(s,1H), 10.04(s,1H), 9.81(s,1H), 6.88(s,1H), 5.17(d,1H), 4.71 (s,1H), 4.58(s,1H), 4.53(d,1H), 3.72(dd,1H), 3.26(dd,1H), 1.51(s,3H);LC-MS(ESI):m / z=512(M+H) +

[0255] Example 84 (2S,3R,5R)-3-(((2-(2,5-dichloro-3,4-dihydroxybenzoyl)hydrazinecarbonyl)oxy)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0256] The title compound was prepared using a similar procedure as described in Example 69, except using 2,5-dichloro-3,4-dihydroxybenzohydrazide instead of 3,4-dihydroxybenzohydrazide. 1H NMR (400MHz, DMSO-d6)δ 13.87(br,1H), 10.35(s,1H), 10.20(s,1H), 10.02(s,1H), 9.59(s,1H), 6.92(s,1H), 5.17(d,1H), 4.71 (s,1H), 4.58(s,1H), 4.53(d,1H), 3.72(dd,1H), 3.26(dd,1H), 1.48(s,3H);LC-MS(ESI):m / z=512(M+H) +

[0257] Example 85 (2S,3R,5R)-3-(((2-(2-fluoro-3,4-dihydroxybenzoyl)hydrazinecarbonyl)oxy)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0258] The title compound was prepared using a similar procedure as described in Example 69, except using 2-fluoro-3,4-dihydroxybenzohydrazide instead of 3,4-dihydroxybenzohydrazide. 1 H NMR (400MHz, DMSO-d6)δ 13.85(br,1H), 10.07(s,1H), 9.83(s,1H), 9.47(s,1H), 9.29(s,1H), 6.99(t,1H), 6.67(d,1H), 5.17(d,1H) , 4.71(s,1H), 4.58(s,1H), 4.53(d,1H), 3.72(dd,1H), 3.26(d,1H), 1.51(s,3H);LC-MS(ESI):m / z=462(M+H) +

[0259] Example 86 (2S,3R,5R)-3-(((2-(3-(3,4-dihydroxyphenyl)propanoyl)hydrazinecarbonyl)oxy)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0260] The title compound was prepared using a similar procedure as described in Example 69, except 3-(3,4-dihydroxyphenyl)propanehydrazide was used instead of 3,4-dihydroxybenzohydrazide. 1 H NMR (400MHz, DMSO-d6)δ 13.83(br,1H), 9.69(s,1H), 9.28(s,1H), 8.84(s,1H), 8.71(s,1H), 6.82(d,1H), 6.57(s,1H), 6.45(d,1H), 5.12(d,1H), 4.65(d ,1H), 4.50(s,1H), 4.38(d,1H), 3.68(dd,1H), 3.26(dd,1H), 2.64(t,2H), 2.31(t,2H), 1.48(s,3H);LC-MS(ESI):m / z=472(M+H) +

[0261] Example 87 (2S,3R,5R)-3-(((2-(2-chloro-4,5-dihydroxybenzoyl)hydrazinecarbonyl)oxy)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0262] The title compound was prepared using a similar procedure as described in Example 69, except using 2-chloro-4,5-dihydroxybenzohydrazide instead of 3,4-dihydroxybenzohydrazide. 1H NMR (400MHz, DMSO-d6)δ 13.85(br,1H), 9.99(s,1H), 9.82(s,1H), 9.56(s,1H), 9.52(s,1H), 6.88(s,1H), 6.80(s,1H), 5.16(d,1H), 4.68(d,1H), 4.57(s,1H), 4.54(d,1H), 3.61(dd,1H), 3.26(dd,1H), 1.50(s,3H);LC-MS(ESI):m / z=478(M+H) +

[0263] Example 88 (2S,3R,5R)-3-((((E)-2-(3,4-dihydroxybenzylidene)hydrazinecarbonyl)oxy)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0264] The title compound was prepared using a similar procedure as described in Example 69, except using (E)-4-(hydrazonomethyl)benzene-1,2-diol instead of 3,4-dihydroxybenzohydrazide. 1 H NMR (400MHz, DMSO-d6)δ 13.84(br,1H), 11.11(s,1H), 9.33(s,1H), 9.22(s,1H), 7.92(s,1H), 7.12(s,1H), 8.84(d,1H), 8.75(d,1H), 5.17( d,1H), 4.71(s,1H), 4.58(s,1H), 4.53(d,1H), 3.72(dd,1H), 3.26(dd,1H), 1.51(s,3H);LC-MS(ESI):m / z=428(M+H) +

[0265] Example 89 (2S,3R,5R)-3-(((2-(3-chloro-4,5-dihydroxybenzoyl)hydrazinecarbonyl)oxy)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0266] The title compound was prepared using a similar procedure as described in Example 69, except using 3,4-bis(benzyloxy)-5-chlorobenzohydrazide instead of 3,4-dihydroxybenzohydrazide. 1 H NMR (400MHz, DMSO-d6)δ 7.28(s,1H), 7.14(s,1H), 7.00(s,1H), 5.57(s,1H), 4.72(d,1H), 4.67(d,2H), 4.39(d,2H), 4.02(s,1H), 3.78(s,1H), 3.46(m,1H), 3.21(m,1H), 1.45(s,3H);LC-MS(ESI):m / z=478(M+H) +

[0267] Example 90 (2S,3R,5R)-3-(((2-(2-(benzo[d][1,3]dioxol-5-yl)acetyl)hydrazinecarbonyl)oxy)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0268] The title compound was prepared using a similar procedure as described in Example 69, except using 2-(benzo[d][1,3]dioxol-5-yl)acetohydrazide instead of 3,4-dihydroxybenzohydrazide. 1H NMR (400MHz, DMSO-d6):δ 13.81(br,1H), 9.92(s,1H), 9.35(s,1H), 6.67(s,1H), 6.63(d,1H), 6.84(s,1H), 5.97(s,2H), 5.13(d,1H), 4.87(s,1H), 4 .47(s,1H), 4.44(d,1H), 3.88(dd,1H), 3.35(s,2H), 3.26(dd,1H), 3.21(dd,1H), 1.48(s,3H);LC-MS(ESI):m / z=470(M+H) +

[0269] Example 91 (2S,3R,5R)-3-(((2-(2-(3,4-dihydroxybenzamido)acetyl)hydrazinecarbonyl)oxy)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0270] The title compound was prepared using procedures similar to those described in Example 95. 1 H NMR (400MHz, DMSO-d6):δ 13.81(br,1H), 9.84(s,1H), 9.12(s,1H), 8.98(s,1H), 8.34(t,1H), 6.87(d,1H), 6.80(s,2H), 6.78(d,1H), 5.13(d,1H), 4.87(s,1H), 4.47(s,1H), 4.44(d,1H), 3.88(dd,1H), 3.67(d,1H), 3.26(dd,1H), 1.48(s,3H);LC-MS(ESI):m / z=501(M+H) +

[0271] Example 92 (2S,3R,5R)-3-(((3-(3,4-dihydroxybenzamido)pyrrolidine-1-carbonyl)oxy)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0272] The title compound was prepared using a similar procedure as described in Example 69, except using 3,4-bis(benzyloxy)-N-(pyrrolidin-3-yl)benzamide instead of 3,4-dihydroxybenzohydrazide. 1 H NMR (400MHz, DMSO-d6)δ 9.87(s,1H), 7.23(d,2H), 6.75(d,1H), 6.67(s,1H), 5.50(s,1H), 4.72(s,1H), 4.67(d,2H), 4.39(d,2H), 3.91(d,2H), 3.81(d,2H), 3.66(d,2H), 3.46(m,1H), 3.21(m,1H), 2.18(m,1H), 1.94(m,1H), 1.45(s,3H);LC-MS(ESI):m / z=498(M+H) +

[0273] Example 93 (2S,3R,5R)-3-(((4-(3,4-dihydroxybenzoyl)piperazine-1-carbonyl)oxy)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0274] The title compound was prepared using a similar procedure as described in Example 69, except using (3,4-bis(benzyloxy)phenyl)(piperazin-1-yl)methanone instead of 3,4-dihydroxybenzohydrazide. 1H NMR (400MHz, DMSO-d6)δ 9.74(s,1H), 7.26(m,1H), 7.19(d,1H), 6.77(d,1H), 4.67(m,2H), 4.39(d,2H), 4.29(s,1H), 3.68-3.5 9(m,4H), 3.59-3.53(m,3H), 3.53-3.44(m,3H), 3.21(m,1H), 1.45(s,3H);LC-MS(ESI):m / z=498(M+H) +

[0275] Example 94 (2S,3R,5R)-3-(((2-(2-(2-chloro-3,4-dihydroxybenzamido)acetyl)hydrazinecarbonyl)oxy)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0276] The title compound was prepared using procedures similar to those described in Example 95. 1 H NMR (400MHz, DMSO-d6):δ 13.83(br,1H), 9.84(s,1H), 9.42(s,1H), 9.25(s,1H), 8.34(t,1H), 6.87(m,3H), 5.13(d,1H), 4.67(d,1H), 4.47(s,1H), 4.44(d,1H), 3.86(d,2H), 3.67(d,1H), 3.26(dd,1H), 1.48(s,3H);LC-MS(ESI):m / z=535(M+H) +

[0277] Example 95 (2S,3R,5R)-3-((((2-(2-chloro-3,4-dihydroxybenzamido)ethyl)carbamoyl)oxy)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0278] FIG. 10 shows a synthetic scheme for preparing this compound. Step 1: tert-Butyl (2-(3,4-bis(benzyloxy)-2-chlorobenzamido)ethyl)carbamate 3,4-Bis(benzyloxy)-2-chlorobenzoic acid (1.0 g, 2.71 mmol) was dissolved in DMF (10 mL). The solution was cooled to 5° C. Then tert-butyl (2-aminoethyl)carbamate (433 mg, 2.71 mmol), 1-hydroxybenzotriazole (439 mg, 3.25 mmol), DIPEA (0.9 mL, 5.42 mmol) and 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (623 mg, 3.25 mmol) were added. The mixture was stirred at room temperature for 12 h. The solution was washed with water and extracted with ethyl acetate (100 mL). The organic layer was dried over Na2SO4. The solvent was evaporated under vacuum to give the title compound (1.2 g, 86.7% yield); LC-MS (ESI): m / z=511 (M+H). +

[0279] Step 2: N-(2-aminoethyl)-3,4-bis(benzyloxy)-2-chlorobenzamide hydrochloride tert-Butyl (2-(3,4-bis(benzyloxy)-2-chlorobenzamido)ethyl)carbamate (1.2 g, 2.35 mmol) was dissolved in ethyl acetate (5 mL). The solution was cooled to 5° C. A solution of hydrogen chloride in ethyl acetate (4 M, 10 mL) was then added. The mixture was stirred for 5 h. The ethyl acetate was then evaporated under vacuum to give N-(2-aminoethyl)-3,4-bis(benzyloxy)-2-chlorobenzamide hydrochloride (763 mg, 72.7% yield); LC-MS (ESI): m / z=411 (M+H). +

[0280] Step 3: (2S,3R,5R)-Benzhydryl 3-((((2-(3,4-bis(benzyloxy)-2-chlorobenzamido)ethyl)carbamoyl)oxy)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate 4,4-dioxide (2S,3R,5R)-Benzhydryl 3-methyl-3-((((4-nitrophenoxy)carbonyl)oxy)methyl)-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate 4,4-dioxide (980 mg, 1.69 mmol) and N-(2-aminoethyl)-3,4-bis(benzyloxy)-2-chlorobenzamide hydrochloride (760 mg, 1.69 mmol) were added to a solution of DMF (20 mL) and pyridine (1 mL). The mixture was stirred at room temperature for 12 h. The solution was washed with water and extracted with ethyl acetate (100 mL). The organic layer was dried over Na2SO4. The solvent was evaporated under vacuum. The residue was purified by column chromatography (silica gel, DCM:MeOH=50:1) to give the title compound (300 mg, 20.7% yield); LC-MS (ESI): m / z=852 (M+H). +

[0281] Step 4: (2S,3R,5R)-3-((((2-(2-chloro-3,4-dihydroxybenzamido)ethyl)carbamoyl)oxy)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide (2S,3R,5R)-Benzhydryl 3-((((2-(3,4-bis(benzyloxy)-2-chlorobenzamido)ethyl)carbamoyl)oxy)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate 4,4-dioxide (300 mg, 0.35 mmol) was dissolved in THF (5 mL). The mixture was degassed twice with N2, Pd / C (10%, 150 mg) was added to the mixture, then the flask was degassed twice with H2 and stirred at room temperature for 12 h. The solution was filtered and the filtrate was concentrated. Ethyl acetate (10 mL) was added and stirred for 30 min. The slurry was filtered and the cake was washed with MTBE (20 ml) to give the title compound (110 mg, 43% yield). 1 H NMR (400MHz, DMSO-d6)δ 13.84(br,1H), 9.92(s,1H), 9.17(s,1H), 8.09(t,1H), 6.67(d,1H), 6.64(d,1H), 5.12(d,1H), 4.65(d,1H), 4.50(s ,1H), 4.38(d,1H), 3.68(dd,1H), 3.26(dd,1H), 3.24(m,1H), 3.15(m,1H), 1.48(s,3H);LC-MS(ESI):m / z=506(M+H) +

[0282] Example 96 (2S,3R,5R)-3-(((4-(3,4-dihydroxybenzamido)piperidine-1-carbonyl)oxy)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0283] The title compound was prepared using a similar procedure as described in Example 69, except using 3,4-bis(benzyloxy)-N-(pyrrolidin-3-yl)benzamide instead of 3,4-dihydroxybenzohydrazide. 1H NMR (400MHz, DMSO-d6)δ 7.28(m,1H), 7.17(s,1H), 6.75(m,1H), 5.50(s,1H), 4.72(t,1H), 4.67(d,2H), 4.39(d,2H), 4.09(m,1H), 3.80(s,1H), 3.77-3.73( m,2H), 3.55-3.50(m,2H), 3.45(d,2H), 3.21(m,1H), 2.25-2.14(m,2H), 1.88-1.80(m,2H), 1.45(s,3H);LC-MS(ESI):m / z=498(M+H) +

[0284] Example 97 (2S,3R,5R)-3-((((1-(3,4-dihydroxybenzoyl)pyrrolidin-3-yl)carbamoyl)oxy)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0285] The title compound was prepared using a similar procedure as described in Example 69, except using 3,4-bis(benzyloxy)-N-(piperidin-4-yl)benzamide instead of 3,4-dihydroxybenzohydrazide. 1 H NMR (400MHz, DMSO-d6)δ 9.88(s,1H), 7.21(d,2H), 6.75(d,1H), 4.94(m,1H), 4.72(t,1H), 4.67(d,2H), 4.39(d,2H), 4.15(s,1H), 3.87(m,1H), 3.76(m,1H), 3.61(d,2H), 3.46(s,1H), 3.21(m,1H), 2.97(s,1H), 2.92(s,1H), 2.16(m,1H), 1.90(m,1H), 1.45(s,3H)LC-MS(ESI): m / z=498(M+H) +

[0286] Example 98 (2S,3R,5R)-3-(((3-(3,4-dihydroxybenzamido)azetidine-1-carbonyl)oxy)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0287] The title compound was prepared using a similar procedure as described in Example 69, except using N-(azetidin-3-yl)-3,4-dihydroxybenzamide instead of 3,4-dihydroxybenzohydrazide. 1 H NMR (400MHz, DMSO-d6)δ 7.23(m,2H), 6.77(d,1H), 6.25(s,1H), 4.70(t,1H), 4.64(d,1H), 4.39(d,2H), 4.32(d,2H), 4.24-4.20( m,1H), 4.02-3.93(m,2H), 3.56(s,1H), 3.46(m,1H), 3.21(m,1H), 1.45(s,3H)LC-MS(ESI): m / z=484(M+H) +

[0288] Example 99 (2S,3R,5R)-3-(5-((2-chloro-3,4-dihydroxybenzamido)methyl)isoxazol-3-yl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0289] FIG. 11 shows a synthetic scheme for preparing this compound. Step 1: 2-chloro-3,4-bis((4-methoxybenzyl)oxy)-N-(prop-2-yn-1-yl)benzamide To a solution of 2-chloro-3,4-bis((4-methoxybenzyl)oxy)benzoic acid (1 g, 2.3 mmol) in DMF (20 mL) was added propargylamine (0.16 g, 2.8 mmol), EDCI (0.72 g, 4.6 mmol), HOBT (0.31 g, 2.3 mmol), followed by NMM (0.71 g, 6.9 mmol). The mixture was stirred at room temperature for 6 hours. The solution was then poured into ice water. The mixture was stirred for 0.5 hours and filtered under reduced pressure. The filter cake was collected and dried to give the title compound as a pale solid (0.91 g, 85% yield).

[0290] Step 2: (2S,3R,5R)-Benzhydryl 3-(5-((2-chloro-3,4-bis((4-methoxybenzyl)oxy)benzamido)methyl)isoxazol-3-yl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate 4,4-dioxide To a solution of (2S)-benzhydryl 3-((Z)-chloro(hydroxyimino)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate 4,4-dioxide (500 mg, 1.07 mmol) in DMF (5 mL), 2-chloro-3,4-bis((4-methoxybenzyl)oxy)-N-(prop-2-yn-1-yl)benzamide (520 mg, 1.2 mmol) and 1,1,1,3,3,3-hexabutyldistannoxane (313 mg, 0.53 mmol) were added. The solution was stirred at room temperature for 2 hours. The solvent was evaporated under vacuum and the residue was purified by column chromatography (silica gel, PE:EtOAc=5:1) to give the title compound as a white solid (524 mg, 56% yield).

[0291] Step 3: (2S,3R,5R)-3-(5-((2-chloro-3,4-dihydroxybenzamido)methyl)isoxazol-3-yl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide To a solution of (2S)-benzhydryl 3-(5-(2-(2-chloro-3,4-bis((4-methoxybenzyl)oxy)phenyl)-2-oxoethyl)isoxazol-3-yl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate 4,4-dioxide (175 mg, 0.20 mmol) in THF (10 mL) was added Pd / C (10%, 50 mg). The solution was stirred at room temperature for 12 hours. The mixture was filtered, the filtrate was evaporated under vacuum, and the residue was washed with MTBE (20 mL) to give a pale solid (74 mg, 79% yield). 1 H NMR (400MHz, DMSO-d6)δ 7.23(d,1H), 6.92(s,1H), 6.66(d,1H), 6.61(s,1H), 4.87(s,1H), 4.70(t,1H), 4.61(s,1H), 4.55(s ,1H), 4.42(s,1H), 4.27(s,1H), 3.46(m,1H), 3.21(m,1H), 1.76(m,3H);LC-MS(ESI):m / z=471(M+H) +

[0292] Example 100 (2S,3R,5R)-3-(5-((3,4-dihydroxybenzamido)methyl)isoxazol-3-yl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0293] The title compound was prepared using a procedure similar to that described in Example 99, except using 3,4-bis((4-methoxybenzyl)oxy)-N-(prop-2-yn-1-yl)benzamide instead of 2-chloro-3,4-bis((4-methoxybenzyl)oxy)-N-(prop-2-yn-1-yl)benzamide. 1H NMR (400MHz, DMSO-d6)δ 7.06(dd,1H), 6.97(d,1H), 6.54(s,1H), 6.37(s,1H), 6.21(s,1H), 4.65(s,1H), 4.48(t,1H), 4.40(s,1H), 4.19(s,1H), 4.05(s,1H), 3.32(s,1H), 3.24(m,1H), 2.99(m,1H), 1.58(s,3H);LC-MS(ESI):m / z=452(M+H) +

[0294] Example 101 (2S,3R,5R)-3-(5-(2-chloro-3,4-dihydroxyphenyl)isoxazol-3-yl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0295] FIG. 12 shows a synthetic scheme for preparing this compound. Step 1: 4,4'-(((3-chloro-4-ethynyl-1,2-phenylene)bis(oxy))bis(methylene))bis(methoxybenzene) To a solution of 2-chloro-3,4-bis((4-methoxybenzyl)oxy)benzaldehyde (2.1 g, 5.1 mmol) in MeOH (10 mL) was added dimethyl (1-diazo-2-oxopropyl)phosphonate (1.2 g, 6.2 mmol). The mixture was stirred at room temperature for 4 h. The solvent was then evaporated under vacuum and the residue was purified by column chromatography (silica gel, PE:EtOAc=20:1) to give a white solid (1.0 g, 48% yield).

[0296] Step 2: (2S,3R,5R)-Benzhydryl 3-(5-(2-chloro-3,4-bis((4-methoxybenzyl)oxy)phenyl)isoxazol-3-yl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate 4,4-dioxide To a solution of (2S,3R,5R)-benzhydryl 3-((Z)-chloro(hydroxyimino)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate 4,4-dioxide (400 mg, 0.86 mmol) in DMF (5 mL) was added a mixture of 4,4'-(((3-chloro-4-ethynyl-1,2-phenylene)bis(oxy))bis(methylene))bis(methoxybenzene) (600 mg, 1.5 mmol) and 1,1,1,3,3,3-hexabutyldistannoxane (260 mg, 0.44 mmol). The solution was stirred at room temperature for 2 hours. The solvent was evaporated under vacuum and the residue was purified by column chromatography (silica gel, PE:EtOAc=5:1) to give a white solid (130 mg, 18% yield). LC-MS: m / z=835 (M+H) +

[0297] Step 3: (2S,3R,5R)-3-(5-(2-chloro-3,4-dihydroxyphenyl)isoxazol-3-yl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide To a solution of (2S,3R,5R)-benzhydryl 3-(5-(2-chloro-3,4-bis((4-methoxybenzyl)oxy)phenyl)isoxazol-3-yl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate 4,4-dioxide (130 mg, 0.16 mmol) in EtOAc (10 mL) was added Pd / C (10%, 50 mg). The solution was stirred at room temperature for 2 hours. The mixture was filtered, the filtrate was evaporated under vacuum, and the residue was washed with MTBE (20 mL) to give a pale solid (20 mg, 29% yield). 1 H NMR (400MHz, DMSO-d6)δ 10.63(s,H), 9.61(s,1H), 7.34(d,2H), 6.90(d,1H), 5.51(s,1H), 5.32(s ,1H), 3.83(m,1H), 3.43(d,1H), 1.94(s,3H);LC-MS(ESI):m / z=429(M+H) +

[0298] Example 102 (2S,3R,5R)-3-(5-(2-(2,5-dichloro-3,4-dihydroxyphenyl)-2-oxoethyl)isoxazol-3-yl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0299] The title compound was prepared using a procedure similar to that described in Example 99, except using 2,5-dichloro-3,4-bis((4-methoxybenzyl)oxy)-N-(prop-2-yn-1-yl)benzamide instead of 2-chloro-3,4-bis((4-methoxybenzyl)oxy)-N-(prop-2-yn-1-yl)benzamide. 1 H NMR (400MHz, DMSO-d6)δ 7.16(s,1H), 6.57(s,1H), 4.87(s,1H), 4.70(t,1H), 4.51(s,1H), 4.37(s,1H), 4.33(m,2H), 3.46(m,1H), 3.21(m,1H), 1.76(s,3H);LC-MS(ESI):m / z=505(M+H) +

[0300] Example 103 (2S,3R,5R)-3-(5-(3,4-dihydroxyphenyl)isoxazol-3-yl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0301] The title compound was prepared using a procedure similar to that described in Example 101, except using 4,4'-(((4-ethynyl-1,2-phenylene)bis(oxy))bis(methylene))bis(methoxybenzene) instead of 4,4'-(((3-chloro-4-ethynyl-1,2-phenylene)bis(oxy))bis(methylene))bis(methoxybenzene). 1 H NMR (400MHz, DMSO-d6)δ 10.62(s,H), 9.62(s,1H), 7.32(d,1H), 7.11(s,1H), 6.89(d,1H), 5.78(s,1H), 5.45(s ,1H), 5.30(s,1H), 3.83(m,1H), 3.43(d,2H), 1.90(s,3H);LC-MS(ESI):m / z=395(M+H) +

[0302] Example 104 (2S,3R,5R)-3-(5-(2-((2-chloro-3,4-dihydroxybenzoyl)oxy)ethyl)isoxazol-3-yl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0303] FIG. 13 shows a synthetic scheme for preparing this compound. Step 1: But-3-yn-1-yl 2-chloro-3,4-bis((4-methoxybenzyl)oxy)benzoate To a solution of 2-chloro-3,4-bis((4-methoxybenzyl)oxy)benzoic acid (2.1 g, 5 mmol) in CHCl (20 mL) was added 1,3-dicyclohexylcarbodiimide (2.1 g, 10 mmol) and N,N-dimethylpyridin-4-amine (1.2 g, 5 mmol). The mixture was stirred at room temperature for 8 h. The solvent was then evaporated under vacuum and the residue was purified by column chromatography (silica gel, PE:EtOAc=20:1) to give a white solid (1.2 g, 53% yield).

[0304] Step 2: (2S,3R,5R)-Benzhydryl 3-(5-(2-((2-chloro-3,4-bis((4-methoxybenzyl)oxy)benzoyl)oxy)ethyl)isoxazol-3-yl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate 4,4-dioxide To a solution of but-3-yn-1-yl 2-chloro-3,4-bis((4-methoxybenzyl)oxy)benzoate (480 mg, 1 mmol) in tolu (10 mL) was added (2S,3R,5R)-benzhydryl 3-((Z)-chloro(hydroxyimino)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate 4,4-dioxide (690 mg, 1.5 mmol). The solution was stirred at room temperature for 3 hours. The solvent was evaporated under vacuum and the residue was purified by column chromatography (silica gel, PE:EtOAc=3:1) to give a white solid (230 mg, 25% yield); LC-MS: m / z=907 (M+H). +

[0305] Step 3: (2S,3R,5R)-3-(5-(2-((2-chloro-3,4-dihydroxybenzoyl)oxy)ethyl)isoxazol-3-yl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide To a solution of (2S,3R,5R)-benzhydryl 3-(5-(2-((2-chloro-3,4-bis((4-methoxybenzyl)oxy)benzoyl)oxy)ethyl)isoxazol-3-yl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate 4,4-dioxide (230 mg, 0.25 mmol) in THF (10 mL) was added Pd / C (10%, 50 mg). The solution was stirred at room temperature for 12 hours. The mixture was filtered, the filtrate was evaporated under vacuum, and the residue was washed with MTBE (20 mL) to give a pale solid (60 mg, 48% yield). 1H NMR (400MHz, DMSO-d6)δ 10.62(s,H), 9.62(s,1H), 7.32(d,1H), 7.01(d,1H), 5.89(s,1H), 5.33(s,1H), 5.01(s,1 H), 4.23(t,2H), 3.67(m,1H), 3.41-3.20(m,3H), 1.90(s,3H);LC-MS(ESI):m / z=501(M+H) +

[0306] Example 105 (2S,3R,5R)-3-(5-(2,5-dichloro-3,4-dihydroxyphenyl)isoxazol-3-yl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0307] The title compound was prepared using a procedure similar to that described in Example 101, except using 4,4'-(((3,6-dichloro-4-ethynyl-1,2-phenylene)bis(oxy))bis(methylene))bis(methoxybenzene) instead of 4,4'-(((3-chloro-4-ethynyl-1,2-phenylene)bis(oxy))bis(methylene))bis(methoxybenzene). 1 H NMR (400MHz, DMSO-d6) 7.53(s,1H), 7.42(s,1H), 5.52(s,1H), 5.32(s,1H), 3.83(m,1H), 3.41(d,2H), 1.90(s,3H); LC-MS(ESI): m / z=463(M+H) +

[0308] Example 106 (2S,3R,5R)-3-(5-(2-((3,4-dihydroxybenzoyl)oxy)ethyl)isoxazol-3-yl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0309] The title compound was prepared using a procedure similar to that described in Example 104, except that but-3-yn-1-yl 3,4-bis((4-methoxybenzyl)oxy)benzoate was used instead of but-3-yn-1-yl 2-chloro-3,4-bis((4-methoxybenzyl)oxy)benzoate. 1 H NMR (400MHz, DMSO-d6)δ 10.62(s,H), 9.60(s,1H), 8.64(s,1H), 7.33(m,2H), 7.03(d,1H), 5.91(s,1H), 5.32(s,1H), 5.0 1(s,1H), 4.22(t,2H), 3.75(m,1H), 3.40-3.22(m,3H), 1.89(s,3H);LC-MS(ESI):m / z=467(M+H) +

[0310] Example 107 (2S,3R,5R)-3-(5-(2-((2-chloro-3,4-dihydroxybenzoyl)oxy)ethyl)-4,5-dihydroisoxazol-3-yl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0311] The title compound was prepared using a procedure similar to that described in Example 104, except that but-3-yn-1-yl 2-chloro-3,4-bis((4-methoxybenzyl)oxy)benzoate was used instead of but-3-yn-1-yl 2-chloro-3,4-bis((4-methoxybenzyl)oxy)benzoate.

[0312] 1H NMR (400MHz, DMSO-d6)δ 10.60(s,H), 9.56(s,1H), 7.33(d,1H), 7.03(d,1H), 5.32(s,1H), 5.02(s,1H), 4.23(t ,2H), 3.71(m,1H), 3.43-3.24(m,4H), 1.91(s,3H), 1.63(m,2H);LC-MS:m / z=503(M+H) +

[0313] Example 108 (2S,3R,5R)-3-(5-(2-chloro-3,4-dihydroxyphenyl)-4,5-dihydroisoxazol-3-yl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0314] The title compound was prepared using a procedure similar to that described in Example 101, except using 4,4'-(((3-chloro-4-vinyl-1,2-phenylene)bis(oxy))bis(methylene))bis(methoxybenzene) instead of 4,4'-(((3-chloro-4-ethynyl-1,2-phenylene)bis(oxy))bis(methylene))bis(methoxybenzene). 1 H NMR (400MHz, DMSO-d6)δ 10.65(s,H), 9.64(s,1H), 7.32(d,1H), 6.92(d,1H), 5.95(t,1H), 5.52(s,1H), 5.3 3(s,1H), 3.87(m,1H), 3.42-3.25(d,3H), 1.92(s,3H);LC-MS(ESI):m / z=431(M+H) +

[0315] Example 109 (2S,3R,5R)-3-(5-((2,5-dichloro-3,4-dihydroxybenzamido)methyl)-4,5-dihydroisoxazol-3-yl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0316] The title compound was prepared using a procedure similar to that described in Example 101, except that buta-N-allyl-2,5-dichloro-3,4-bis((4-methoxybenzyl)oxy)benzamide was used instead of but-3-yn-1-yl 2-chloro-3,4-bis((4-methoxybenzyl)oxy)benzoate.

[0317] 1 H NMR (400MHz, DMSO-d6)8.62(s,1H)7.02(s,1H),5.33(s,1H),5.04(s,1H),3.70( m,1H), 3.40-3.20(m,4H), 2.74(m,2H), 1.92(s,3H);LC-MS(ESI):m / z=522(M+H) +

[0318] Example 110 (2S,3R,5R)-3-(5-(2-((3,4-dihydroxybenzoyl)oxy)ethyl)-4,5-dihydroisoxazol-3-yl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0319] The title compound was prepared using a procedure similar to that described in Example 104, except that but-3-yn-1-yl 2-chloro-3,4-bis((4-methoxybenzyl)oxy)benzoate was used instead of but-3-yn-1-yl 3,4-bis((4-methoxybenzyl)oxy)benzoate. 1 H NMR (400MHz, DMSO-d6)δ 10.63(s,H), 9.62(s,1H), 7.23(m,2H), 7.01(d,1H), 5.31(s,1H), 5.01(s,1H), 4.22(t,2 H), 3.72(m,1H), 3.42-3.24(m,4H), 1.93(s,3H), 1.60(m,2H);LC-MS(ESI):m / z=469(M+H) +

[0320] Example 111 (2S,3R,5R)-3-(5-((2-chloro-3,4-dihydroxybenzamido)methyl)-4,5-dihydroisoxazol-3-yl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0321] The title compound was prepared using a procedure similar to that described in Example 101, except that buta-N-allyl-2-chloro-3,4-bis((4-methoxybenzyl)oxy)benzamide was used instead of but-3-yn-1-yl 2-chloro-3,4-bis((4-methoxybenzyl)oxy)benzoate. 1 H NMR (400MHz, DMSO-d6)δ 10.64(s,H), 9.64(s,1H), 8.61(s,1H), 7.32(d,1H), 7.01(d,1H), 5.32(s,1H), 5.04 (s,1H), 3.72(m,1H), 3.40-3.21(m,4H), 2.72(m,2H), 1.92(s,3H);LC-MS(ESI):M / Z m / z=488(M+H) +

[0322] Example 112 (2S,3R,5R)-3-(5-(3,4-dihydroxybenzoyl)isoxazol-3-yl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0323] The title compound was prepared using a procedure similar to that described in Example 101, except using 1-(3,4-bis((4-methoxybenzyl)oxy)phenyl)prop-2-yn-1-one instead of 4,4'-(((3-chloro-4-ethynyl-1,2-phenylene)bis(oxy))bis(methylene))bis(methoxybenzene). 1 H NMR (400MHz, DMSO-d6) 7.73(s,1H), 7.45(d,2H), 7.02(d,1H), 5.52(s,1H), 5. 33(s,1H), 3.83(d,1H), 3.72(d,1H), 1.90(s,3H);LC-MS(ESI):m / z=423(M+H) +

[0324] Example 113 (2S,3R,5R)-3-(((3,4-dihydroxybenzoyl)oxy)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0325] FIG. 14 shows a synthetic scheme for preparing this compound. Step 1. (R)-Benzhydryl 2-((R)-2-(benzo[d]thiazol-2-yldisulfanyl)-4-oxoazetidin-1-yl)-3-methylbut-3-enoate (2S,4R,5R)-Benzhydryl 3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate 4-oxide (5 g, 13.0 mmol) and 2-mercaptobenzothiazole (2.17 g, 13.0 mmol) were dissolved in 40 mL of toluene and 40 mL of cyclohexane in a round-bottom flask. The mixture was stirred at 100° C. for 10 h. The solvent was then evaporated under vacuum. EtOAc (100 mL) was added and the organic layer was dried over Na2SO4. The solvent was then evaporated under vacuum. LC-MS (ESI): m / z=533 (M+H) +

[0326] Step 2. (2S,3R,5R)-Benzhydryl 3-(((3,4-bis(benzyloxy)benzoyl)oxy)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate 3,4-Bis(benzyloxy)benzoic acid (4.3 g, 13.0 mmol) and silver acetate (4.3 g, 26.0 mmol) were dissolved in DCM (75 mL) in a round bottom flask. (R)-Benzhydryl 2-((R)-2-(benzo[d]thiazol-2-yldisulfanyl)-4-oxoazetidin-1-yl)-3-methylbut-3-enoate (6.9 g, 13.0 mmol) was dissolved in DCM (25 mL) and then added dropwise to the solution. The mixture was stirred at 25° C. for 12 h. The solvent was filtered and the mother liquor was evaporated under vacuum. The solution was washed with water and extracted with EtOAc (200 mL). The organic layer was dried over Na2SO4. The solvent was evaporated under vacuum. The residue was purified by column chromatography (silica gel, hexane:EtOAc=3:1) to give the title compound (2.2 g, 24.2% yield); LC-MS (ESI): m / z=700 (M+H). +

[0327] Step 3. (2S,3R,5R)-Benzhydryl 3-(((3,4-bis(benzyloxy)benzoyl)oxy)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate 4,4-dioxide (2S,3R,5R)-Benzhydryl 3-(((3,4-bis(benzyloxy)benzoyl)oxy)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate (2.2 g, 3.1 mmol) was dissolved in acetic acid (15 mL), acetone (3 mL) and H2O (3 mL) in a round bottom flask. The mixture was stirred at 10°C for 4 h. EtOAc (100 mL) was added to the solvent. Sodium metabisulfite solution was then added slowly. The solution was extracted with EtOAc (100 mL). The organic layer was dried over Na2SO4. The solvent was evaporated under vacuum. The residue was purified by column chromatography (silica gel, hexane:EtOAc = 3:1) to give the title compound (680 mg, 30.0% yield); LC-MS (ESI): m / z = 732 (M + H). +

[0328] Step 4: (2S,3R,5R)-3-(((3,4-dihydroxybenzoyl)oxy)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide (2S,3R,5R)-Benzhydryl 3-(((3,4-bis(benzyloxy)benzoyl)oxy)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate 4,4-dioxide was dissolved in THF (30 mL), Pd / C (10%, 500 mg) was added, and the solution was stirred under a hydrogen-filled balloon for 10 h. Palladium was removed by filtration, then the solvent was evaporated under vacuum, and the residue was purified by silica gel (DCM:MeOH=20:1) to give a white solid (205 mg, 57.3% yield). 1 H NMR (400MHz, DMSO-d6)δ 9.91(s,1H), 9.41(s,1H), 7.38(md,2H), 6.84(d,1H), 5.19(d,1H), 4.76(d,1H), 4.66(m,2H), 3.71(dd,1H), 3.32(d,2H), 1.55(s,3H);LC-MS(ESI):m / z=386(M+H) +

[0329] Example 114 (2S,3R,5R)-3-(((2-chloro-3,4-dihydroxybenzoyl)oxy)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0330] The title compound was prepared using a similar procedure as described in Example 113, except 3,4-bis(benzyloxy)-2-chlorobenzoic acid was used instead of 3,4-bis(benzyloxy)benzoic acid. 1 H NMR (400MHz, DMSO-d6)δ 10.64(s,1H), 9.45(s,1H), 7.39(d,1H), 6.83(d,1H), 5.18(d,1H), 4.76(d,1H), 4.68(t,2H), 3.71(dd,1H), 3.3(d,2H), 1.55(s,3H), LC-MS(ESI): m / z=420(M+H) +

[0331] Example 115 (2S,3S,5R)-3-((3,4-dihydroxybenzamido)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0332] FIG. 15 shows a synthetic scheme for preparing this compound. Step 1. (2S,3S,5R)-Benzhydryl 3-(((4-methoxybenzyl)amino)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate (2S,3R,5R)-Benzhydryl 3-(chloromethyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate (10 g, 24.9 mmol) in acetonitrile (90 mL) and water (30 mL) was added 4-methoxybenzylamine (3.4 g, 24.9 mmol). Sodium bicarbonate (4.2 g, 49.8 mmol) was then added. The mixture was stirred at room temperature for 16 h. The solution was washed with water and extracted with EtOAc (100 mL). The organic layer was dried over Na2SO4. The solvent was evaporated under vacuum. The residue was purified by column chromatography (silica gel, DCM:MeOH=100:1) to give the title compound (4.0 g, 32% yield); LC-MS (ESI): m / z=503 (M+H). +

[0333] Step 2: (2S,3S,5R)-Benzhydryl 3-((3,4-bis(benzyloxy)-N-(4-methoxybenzyl)benzamido)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate To a solution of (2S,3S,5R)-benzhydryl 3-(((4-methoxybenzyl)amino)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate (4.0 g, 7.96 mmol) in dry acetonitrile (100 mL) was added triethylamine (2.06 mL, 15.92 mmol). The solution was cooled to 5° C., then 3,4-bis(benzyloxy)benzoyl chloride (4.2 g, 11.95 mmol) was added dropwise. The mixture was stirred at 5° C. for 6 hours, then allowed to warm to room temperature for 16 hours. The solution was washed with water and extracted with ethyl acetate (100 mL). The organic layer was dried over Na2SO4. The solvent was evaporated under vacuum. The residue was purified by column chromatography (silica gel, DCM:MeOH=100:1) to give the title compound (1.2 g, 18.4% yield); LC-MS (ESI): m / z=819 (M+H). +

[0334] Step 3: (2S,3S,5R)-Benzhydryl 3-((3,4-bis(benzyloxy)benzamido)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate (2S,3S,5R)-Benzhydryl 3-((3,4-bis(benzyloxy)-N-(4-methoxybenzyl)benzamido)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate (1.0 g, 1.22 mmol) was dissolved in acetonitrile (10 mL). Water (10 mL) and ceric ammonium nitrate (2.0 g, 3.66 mmol) were added. The mixture was stirred for 5 h. The solution was washed with water and extracted with ethyl acetate (50 mL). The organic layer was dried over Na2SO4. The solvent was evaporated under vacuum. The residue was purified by column chromatography (silica gel, DCM:MeOH=50:1) to give the title compound (570 mg, 67% yield); LC-MS (ESI): m / z=699 (M+H). +

[0335] Step 4: (2S,3S,5R)-Benzhydryl 3-((3,4-bis(benzyloxy)benzamido)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate 4,4-dioxide (2S,3S,5R)-Benzhydryl 3-((3,4-bis(benzyloxy)benzamido)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate (570 mg, 0.82 mmol) was dissolved in acetic acid (10 mL). Water (2 mL) and acetone (2 mL) were then added. The solution was cooled to 5° C. KMnO4 (259 mg, 1.64 mmol) was added in portions. The mixture was stirred at 5° C. for 3 h. The solution was washed with water and extracted with ethyl acetate (50 mL). The organic layer was dried over Na2SO4. The solvent was evaporated under vacuum to give the title compound (478 mg, 80% yield); LC-MS (ESI): m / z=731 (M+H). +

[0336] Step 5: (2S,3S,5R)-3-((3,4-dihydroxybenzamido)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide (2S,3S,5R)-Benzhydryl 3-((3,4-bis(benzyloxy)benzamido)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate 4,4-dioxide (478 mg, 0.65 mmol) was dissolved in THF (5 mL). The mixture was degassed twice with N2, Pd / C (10%, 150 mg) was added, then the flask was degassed twice with H2 and stirred at room temperature for 12 h. The solution was filtered and the filtrate was concentrated. Ethyl acetate (10 mL) was added and stirred for 30 min. The slurry was filtered and the cake was washed with MTBE (20 mL) to give the title compound (100 mg, 40% yield). 1 H NMR (400MHz, DMSO-d6)δ 13.84(br,1H), 9.45(s,1H), 9.34(s,1H), 7.82(br,1H), 6.88(d,1H), 6.86(s,1H), 6.81(d,1H), 5.47(d,1H), 4.72(s,1H), 4.11(d,1H), 3.56(d,1H), 3.52(dd,1H), 2.67(dd,1H), 1.51(s,3H);LC-MS(ESI):m / z=385(M+H) +

[0337] Example 116 (2S,3S,5R)-3-(acetamidomethyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0338] The title compound was prepared using procedures similar to those described in Example 115. 1H NMR (400MHz, DMSO-d6)δ 12.84(br,1H), 5.47(d,1H), 4.72(s,1H), 4.11(d,1H), 3.56(d,1H), 3.52(d d,1H), 2.67(dd,1H), 2.25(s,3H), 1.51(s,3H);LC-MS(ESI):m / z=291(M+H) +

[0339] Example 117 (2S,3S,5R)-3-(((3,4-dihydroxyphenyl)amino)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0340] FIG. 16 shows a synthetic scheme for preparing this compound. Step 1. 4-Aminobenzene-1,2-diol To a solution of 4-amino-2-methoxyphenol (1000 mg, 7.19 mmol) in dichloromethane (20 mL) was added boron tribromide (2162 mg, 8.63 mmol). The reaction mixture was stirred at 0° C. for 2 h. The crude was then purified by column chromatography (silica gel) to give the title compound (810 mg, 90% yield); LC-MS (ESI): m / z=247 (M+H). +

[0341] Step 2. (2S,3S,5R)-Benzhydryl 3-(((3,4-dihydroxyphenyl)amino)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate 4,4-dioxide To a solution of 4-aminobenzene-1,2-diol (30 mg, 0.24 mmol) in MeOH (2 mL), (2S,3R,5R)-benzhydryl 3-formyl-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate 4,4-dioxide (100 mg, 0.24 mmol) and sodium borohydride (18 mg, 0.48 mmol) were added. The crude was then purified by column chromatography (silica gel) to give the title compound (78 mg, 62% yield); LC-MS (ESI): m / z=523 (M+H). +

[0342] Step 3. (2S,3S,5R)-3-(((3,4-dihydroxyphenyl)amino)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide To a solution of (2S,3S,5R)-benzhydryl 3-(((3,4-dihydroxyphenyl)amino)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate 4,4-dioxide (78 mg, 0.15 mmol) in MeOH (2 mL) was added Pd / C (10%, 30 mg). The reaction mixture was evacuated and inflated with a hydrogen balloon. After stirring for 12 h, 18 mg of product was purified by flash chromatography in 33% yield. 1 H NMR (400MHz, DMSO-d6)δ 6.95(d,1H), 6.87(d,1H), 6.36(d,1H), 7.04(d,1H), 5.55(s,2H), 4.20(s,1H), 4.50(s,1H), 4.10(s,1H), 3.57(m,4H), 3.41(m,2H), 3.21(m,2H), 1.50(s,3H);LC-MS(ESI):m / z=357(M+H) +

[0343] Example 118 (2S,3R,5R)-3-((E)-((2-(2-chloro-3,4-dihydroxybenzamido)ethoxy)imino)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0344] FIG. 17 shows a synthetic scheme for preparing this compound. Step 1. Benzyl [2-({[(2-methyl-2-propanyl)oxy]carbonyl}amino)ethoxy]carbamate To a solution of tert-butyl (2-(aminooxy)ethyl)carbamate (1650 mg, 9.36 mmol) in THF (10 mL) was added NaHCO3 (865 mg, 10.30 mmol) and Cbz-Cl (1597 mg, 9.36 mmol). The reaction mixture was stirred at room temperature for 4 h and purified by flash chromatography to give 2530 mg of product in 87% yield. LC-MS (ESI): m / z=311 (M+H). +

[0345] Step 2. Benzyl 2-aminoethoxycarbamate 3.2 mL of 4M HCl was added to a solution of benzyl [2-({[(2-methyl-2-propanyl)oxy]carbonyl}amino)ethoxy]carbamate (1000 mg, 3.22 mmol) in ethyl acetate (5 mL). The reaction mixture was stirred at room temperature for 12 h. After evaporation, 630 mg of the crude product was used in the next step without further purification. LC-MS (ESI): m / z=211 (M+H). +

[0346] Step 3. Benzyl 2-(2-chloro-3,4-dimethoxybenzamido)ethoxycarbamate N'-(Ethylkohlenstoffimidoyl)-N,N-dimethylpropan-1,3-diaminhydrochlorid (383 mg, 2.00 mmol) was added to a solution of benzyl 2-aminoethoxycarbamate (210 mg, 1.00 mmol), 2-chloro-3,4-dimethoxybenzoic acid (217 mg, 1.00 mmol), 1-hydroxybenzotriazole (135 mg, 1.00 mmol) and 4-methylmorpholine (202 mg, 2.00 mmol) in N,N-dimethylformamide (5 mL). The reaction mixture was stirred for 12 h. 280 mg of product was obtained by flash chromatography in 68% yield. LC-MS (ESI): m / z=409 (M+H) +

[0347] Step 4. N-(2-(aminooxy)ethyl)-2-chloro-3,4-dihydroxybenzamide To a solution of benzyl 2-(2-chloro-3,4-dimethoxybenzamido)ethoxycarbamate (250 mg, 0.61 mmol) in dichloromethane (3 mL) was added boron tribromide (613 mg, 2.44 mmol). The reaction mixture was stirred at 0° C. for 2 h. 131 mg of product was obtained by flash chromatography in 87% yield. LC-MS (ESI): m / z=247 (M+H). +

[0348] Step 5. (2S,3R,5R)-Benzhydryl 3-((E)-((2-(2-chloro-3,4-dihydroxybenzamido)ethoxy)imino)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate 4,4-dioxide To a solution of N-(2-(aminooxy)ethyl)-2-chloro-3,4-dihydroxybenzamide (107 mg, 0.44 mmol) in N,N-dimethylformamide (2 mL) was added (2S,3R,5R)-benzhydryl 3-formyl-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate 4,4-dioxide (180 mg, 0.44 mmol) and 0.1 mL of 1M HCl. The reaction mixture was stirred for 12 hours and then poured into ice water. The product was filtered to give 70 mg of a white solid. LC-MS (ESI): m / z=643 (M+H). +

[0349] Step 6: (2S,3R,5R)-3-((E)-((2-(2-chloro-3,4-dihydroxybenzamido)ethoxy)imino)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide To a solution of (2S,3R,5R)-benzhydryl 3-((E)-((2-(2-chloro-3,4-dihydroxybenzamido)ethoxy)imino)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate 4,4-dioxide (70 mg, 0.11 mmol) in tetrahydrofuran (2 mL) was added 10% Pd-C (50 mg). The reaction mixture was evacuated and inflated with a hydrogen balloon. After stirring for 12 h, 15 mg of product was purified by flash chromatography in 29% yield. 1 H NMR (400MHz, DMSO-d6)δ 8.03(s,1H), 7.50(s,1H), 7.36(d,1H), 7.04(d,1H), 5.35(s,2H), 4.70(m,1H), 4.50(s,1H), 3.83(t,2H), 3.46(m,4H), 3.30(m,2H), 3.21(m,2H), 1.45(s,3H);LC-MS(ESI):m / z=476(M+H) +

[0350] Example 119 (2S,3R,5R)-3-((E)-((4-(2-chloro-3,4-dihydroxybenzamido)phenoxy)imino)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0351] FIG. 18 shows a synthetic scheme for preparing this compound. Step 1. tert-Butyl 4-nitrophenoxycarbamate To a solution of O-(4-nitrophenyl)hydroxylamine (2500 mg, 12.22 mmol) in THF (50 mL) was added di-tert-butyl dicarbonate (2780 mg, 12.83 mmol) and triethylamine (3091 mg, 30.56 mmol). The reaction mixture was stirred for 12 h. After evaporation, 3550 mg of the crude product was used in the next step without further purification. LC-MS (ESI): m / z=255 (M+H). +

[0352] Step 2. tert-Butyl 4-aminophenoxycarbamate To a solution of tert-butyl 4-nitrophenoxycarbamate (1000 mg, 3.73 mmol) was added Pd / C (10%, 100 mg). The reaction mixture was evacuated and inflated with a hydrogen balloon. After stirring for 12 h, 552 mg of product was purified by flash chromatography in 62% yield. LC-MS (ESI): m / z=239 (M+H). +

[0353] Step 3. tert-Butyl 4-(2-chloro-3,4-dimethoxybenzamido)phenoxycarbamate To a solution of tert-butyl 4-(2-chloro-3,4-dimethoxybenzamido)phenoxycarbamate (500 mg, 2.10 mmol), 2-chloro-3,4-dimethoxybenzoic acid (455 mg, 2.10 mmol), 4-dimethylaminopyridine (26 mg, 0.21 mmol) was added N'-(ethylkorenstoffimidoyl)-N,N-dimethylpropane-1,3-diamine hydrochloride (483 mg, 2.52 mmol). The reaction mixture was stirred for 12 h and then poured into ice water. The product was filtered to give 510 mg of a white solid. LC-MS (ESI): m / z=423 (M+H) +

[0354] Step 4. N-(4-(aminooxy)phenyl)-2-chloro-3,4-dihydroxybenzamide To a solution of tert-butyl 4-(2-chloro-3,4-dimethoxybenzamido)phenoxycarbamate (1000 mg, 2.32 mmol) in dichloromethane (3 mL) was added boron tribromide (1743 mg, 6.96 mmol). The reaction mixture was stirred at 0° C. for 2 h. 400 mg of product was obtained by flash chromatography in 58% yield. LC-MS (ESI): m / z=247 (M+H). +

[0355] Step 5. (2S,3R,5R)-Benzhydryl 3-((E)-((4-(2-chloro-3,4-dihydroxybenzamido)phenoxy)imino)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate 4,4-dioxide To a solution of N-(4-(aminooxy)phenyl)-2-chloro-3,4-dihydroxybenzamide (400 mg, 1.36 mmol) in N,N-dimethylformamide (5 mL) was added (2S,3R,5R)-benzhydryl 3-formyl-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate 4,4-dioxide (561 mg, 1.36 mmol) and 0.1 mL of 1 M HCl. The reaction mixture was stirred for 12 h and then poured into ice water. The product was filtered to give 220 mg of a white solid. LC-MS (ESI): m / z=691 (M+H). +

[0356] Step 6: (2S,3R,5R)-3-((E)-((4-(2-chloro-3,4-dihydroxybenzamido)phenoxy)imino)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide To a solution of (2S,3R,5R)-benzhydryl 3-((E)-((4-(2-chloro-3,4-dihydroxybenzamido)phenoxy)imino)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate 4,4-dioxide (50 mg, 0.07 mmol) in tetrahydrofuran (2 mL) was added Pd / C (10%, 50 mg). The reaction mixture was evacuated and inflated with a hydrogen balloon. After stirring for 12 h, 16 mg of product was purified by flash chromatography in 43% yield. 1 H NMR (400MHz, DMSO-d6)δ 9.10(s,1H), 7.84(m,1H), 7.51(m,1H), 7.45(dd,2H), 7.05(dd,2H), 5.37(s,2H), 4.76( m,1H), 4.55(s,1H), 3.50(m,2H), 3.25(m,2H), 1.45(s,3H);LC-MS(ESI):m / z=524(M+H) +

[0357] Example 120 (2S,3R,5R)-3-(5-(2-chloro-3,4-dihydroxybenzoyl)isoxazol-3-yl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0358] The title compound was prepared using a procedure similar to that described in Example 101, except using 1-(2-chloro-3,4-bis((4-methoxybenzyl)oxy)phenyl)prop-2-yn-1-one instead of 4,4'-(((3-chloro-4-ethynyl-1,2-phenylene)bis(oxy))bis(methylene))bis(methoxybenzene). 1 H NMR (400MHz, DMSO) 7.52(d,2H), 7.01(d,1H), 5.52(s,1H), 5.32(s,1H), 3.78(d,1H), 3.67(d,1H), 1.92(s,3H); LC-MS(ESI): m / z=457(M+H) +

[0359] Example 121 (2S,3R,5R)-3-((E)-(2-(2-bromo-4,5-dihydroxybenzoyl)hydrazono)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0360] The title compound was prepared using a similar procedure as described in Example 1, except using 2-bromo-4,5-dihydroxybenzohydrazide instead of 2-chloro-4,5-dihydroxybenzohydrazide. 1H NMR (400MHz, DMSO-d6)δ 12.10(s,H), 10.20(s,1H), 9.41(s,1H), 7.79(s,1H), 7.12(s,1H), 6.94(d,1H), 6.83(d,1H), 6.62( s,1H), 5.30(d,1H), 3.74(t,3H), 3.31(m,1H), 2.20(s,1H), 1.62(s,3H);LC-MS(ESI):m / z=475(M+H) +

[0361] Example 122 (2S,3R,5R)-3-((E)-(2-(3-(3,4-dihydroxyphenyl)-5-methylisoxazole-4-carbonyl)hydrazono)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0362] The title compound was prepared using a similar procedure as described in Example 1, except using 3-(3,4-dihydroxyphenyl)-5-methylisoxazole-4-carbohydrazide instead of 2-chloro-4,5-dihydroxybenzohydrazide. 1 H NMR (400MHz, DMSO-d6)δ 12.3(s,1H), 12.1(s,1H), 7.50(s,3H), 7.07(s,1H), 6.99(s,1H), 6.83(s,1H), 5.41(s,1H), 4.70(t,1H), 4.22 (s,1H), 3.66(s,1H), 3.46(dd,1H), 3.21(dd,1H), 2.38-2.34(m,3H), 1.56(s,3H);LC-MS(ESI):m / z=479(M+H) +

[0363] Example 123 (2S,3R,5R)-3-((E)-(2-(3-(2-chloro-3,4-dihydroxyphenyl)isoxazole-5-carbonyl)hydrazono)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0364] The title compound was prepared using a similar procedure as described in Example 1, except 3-(2-chloro-3,4-dihydroxyphenyl)isoxazole-5-carbohydrazide was used instead of 2-chloro-4,5-dihydroxybenzohydrazide. 1 H NMR (400MHz, DMSO-d6) δ 12.2(s,1H), δ 7.56(s,1H), 7.50(s,1H), 7.03(d,1H), 6.69(d,1H), 5.12(s,1H), 4.70(t,1H), 4 .50(dd,1H), 4.25(dd,1H), 3.71(s,1H), 1.78(s,3H);LC-MS(ESI):m / z=499(M+H) +

[0365] Example 124 (2S,3R,5R)-3-((E)-(2-(3-(3,4-dihydroxyphenyl)isoxazole-5-carbonyl)hydrazono)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0366] The title compound was prepared using a similar procedure as described in Example 1, except 3-(3,4-dihydroxyphenyl)isoxazole-5-carbohydrazide was used instead of 2-chloro-4,5-dihydroxybenzohydrazide. 1H NMR (400MHz, DMSO-d6) δ 12.2(s,1H), δ 7.56(s,1H), 7.50(s,1H), 7.10(dd,1H), 7.03(d,1H), 6.69(d,1H), 5.12(s,1H), 4.70(t ,1H), 4.50(dd,1H), 4.25(dd,1H), 3.71(s,1H), 1.65(s,3H);LC-MS(ESI):m / z=465(M+H) +

[0367] Example 125 (2S,3R,5R)-3-((E)-(2-((4S,5R)-2-(2,3-dihydroxyphenyl)-5-methyl-4,5-dihydrooxazole-4-carbonyl)hydrazono)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0368] The title compound was prepared using a procedure similar to that described in Example 1, except that (4S,5R)-2-(2,3-dihydroxyphenyl)-5-methyl-4,5-dihydrooxazole-4-carbohydrazide was used instead of 2-chloro-4,5-dihydroxybenzohydrazide. 1 H NMR (400MHz, DMSO)δ 11.83(d,J=40.2Hz,1H), 9.18(d,J=62.8Hz,1H), 7.47(dd,J=88.7, 55.2Hz,2H), 6.97(d,J=7.7Hz,1H), 6.74(t,J=7.8Hz,1H), 5.11(s,1H), 4.48-4.17(m,2H), 3.60(d,J=15.5Hz,2H), 3.23-3.09(m,3H), 1.58(d,J=7.4Hz,3H);LC-MS(ESI):m / z=481(M+H) +

[0369] Example 126 (2S,3R,5R)-3-((E)-(2-((4S,5R)-2-(3,4-dihydroxyphenyl)-5-methyl-4,5-dihydrooxazole-4-carbonyl)hydrazono)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0370] The title compound was prepared using a procedure similar to that described in Example 1, except that (4S,5R)-2-(3,4-dihydroxyphenyl)-5-methyl-4,5-dihydrooxazole-4-carbohydrazide was used instead of 2-chloro-4,5-dihydroxybenzohydrazide. 1 H NMR (400MHz, DMSO)δ 12.18(s,1H), 7.99(s,1H), 7.30(s,1H), 6.89(d,J=85.4Hz,2H), 5.34(s,1H), 4.98(s,1 H), 3.76(d,J=16.2Hz,2H), 3.45-3.26(m,3H), 1.66(s,3H);LC-MS(ESI):m / z=481(M+H) +

[0371] Example 127 (2S,3R,5R)-3-(((2-(3-(2,3-dihydroxyphenyl)isoxazole-5-carbonyl)hydrazinecarbonyl)oxy)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0372] The title compound was prepared using a similar procedure as described in Example 69, except 3-(2,3-dihydroxyphenyl)isoxazole-5-carbohydrazide was used instead of 3,4-dihydroxybenzohydrazide. 1H NMR (400MHz, DMSO-d6)δ 14.02(br,1H), 11.00(s,1H), 9.88(t,J=12Hz,1H), 9.65-9.19(m,2H), 7.26(t,J= 8Hz,1H), 6.97(t,J=8Hz,1H), 6.83-6.76(m,1H), 5.78(s,1H), 5.17(d,J=12Hz,1H ), 4.74-4.49(m,3H), 3.71-3.68(m,1H), 3.24-3.17(m,2H), 1.49(s,3H);LC-MS(ESI):m / z=511(M+H) +

[0373] Example 128 (2S,3R,5R)-3-(((2-(3-(2,3-dihydroxyphenyl)-4,5-dihydroisoxazole-5-carbonyl)hydrazinecarbonyl)oxy)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0374] The title compound was prepared using a similar procedure as described in Example 69, except 3-(2,3-dihydroxyphenyl)-4,5-dihydroisoxazole-5-carbohydrazide was used instead of 3,4-dihydroxybenzohydrazide. 1H NMR (400MHz, DMSO-d6)δ 13.96(br,1H), 12.57(s,1H), 10.27(s,1H), 9.62(s,1H), 9.53(s,1H), 9.51(s,1H), 9.27(s,1H), 9.21(s,1H), 7.01 (t,J=8Hz,2H), 6.92(t,J=8Hz,2H), 6.76(t,J=8Hz,2H), 5.68(t,J=8Hz,1H), 5.18-5.12(m,2H), 4.67(d,J=12Hz,1H) ), 4.57 (s,1H), 4.50(dt,12, 4Hz,1H), 3.89-3.65(m,6H), 3.28(d,J=16Hz,1H), 1.50(s,3H);LC-MS(ESI):m / z=513(M+H) +

[0375] Example 129 (2S,3R,5R)-3-(((4-(2-chloro-3,4-dihydroxybenzoyl)piperazine-1-carbonyl)oxy)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0376] The title compound was prepared using a similar procedure as described in Example 69, except using (2-chloro-3,4-dihydroxyphenyl)(piperazin-1-yl)methanone instead of 3,4-dihydroxybenzohydrazide. 1 H NMR (400MHz, DMSO-d6)δ 13.96(br,1H), 10.04(s,1H), 9.40(s,1H), 6.81(d,J=8Hz,1H), 6.64(d,J =8Hz,1H), 5.17(s,1H), 4.61-4.50(m,3H), 3.71-3.65(m,3H), 3.49-3.26 (m,8H), 3.18(s,2H), 1.50(s,3H);LC-MS(ESI):m / z=532(M+H) +

[0377] Example 130 (2S,3R,5R)-3-(((3-(2-chloro-3,4-dihydroxybenzamido)azetidine-1-carbonyl)oxy)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0378] The title compound was prepared using a similar procedure as described in Example 69, except using N-(azetidin-3-yl)-2-chloro-3,4-dihydroxybenzamide instead of 3,4-dihydroxybenzohydrazide. 1 H NMR (400MHz, DMSO-d6)δ 10.14(s,1H), 9.36(s,1H), 8.89 (s,1H), 6.81(dd,J=12, 8Hz,2H), 6.60 (dd,J=12, 8Hz,1H), 5.17(s,1H), 4.64-4.58(m,2H), 4.51(dd,J=48, 12Hz,2H), 4.24(br,1H), 3.91(br,1H), 3.70(dd,J=16, 4Hz,2H), 3.31-3.27(m,2H), 2.25(s,1H), 1.51(s,3H);LC-MS(ESI):m / z=518(M+H) +

[0379] Example 131 (2S,3R,5R)-3-(((2-(3-(2-chloro-3,4-dihydroxyphenyl)-4,5-dihydroisoxazole-5-carbonyl)hydrazine-1-carbonyl)oxy)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0380] The title compound was prepared using a similar procedure as described in Example 69, except 3-(2-chloro-3,4-dihydroxyphenyl)-4,5-dihydroisoxazole-5-carbohydrazide was used instead of 3,4-dihydroxybenzohydrazide. 1 H NMR (400MHz, DMSO-d6)δ 9.67(s,1H), 7.51(s,1H), 6.87(d,J=7.5Hz,1H), 6.72(d,J=7.5Hz,1H), 5.79(s,1H) , 5.10(t,J=4.6Hz,1H), 4.74-4.61(m,2H), 4.39(t,J=6.2Hz,2H), 4.26(s,1H), 3.56 (s,1H), 3.46(dd,J=12.4, 8.2Hz,1H), 3.33(dd,J=12.4, 4.5Hz,1H), 3.21(dd,J=12. 3, 8.2Hz, 1H), 3.05 (dd, J=12.5, 4.6Hz, 1H), 1.43 (s, 3H); LC-MS (ESI): m / z=547 (M+H) +

[0381] Example 132 (2S,3R,5R)-3-(((2-(3-(2-chloro-3,4-dihydroxyphenyl)-4,5-dihydroisoxazole-5-carbonyl)hydrazinecarbonyl)oxy)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0382] The title compound was prepared using a similar procedure as described in Example 69, except 3-(2-chloro-3,4-dihydroxyphenyl)isoxazole-5-carbohydrazide was used instead of 3,4-dihydroxybenzohydrazide. 1H NMR (400MHz, DMSO-d6)δ 14.02(br,1H), 10.99(s,1H), 10.38(s,1H), 9.84(s,1H), 9.56(s,1H), 7.52(s,1H), 7.07(d,J=8.4Hz,1H), 6. 90(d,J=8.4Hz,1H), 5.20(d,J=3.2Hz,1H), 4.72(d,J=12.4Hz,1H), 4.62(s,1H), 4.56(d,J=12.8Hz,1H), 3.70 (dd,J=16.4, 4.4Hz,1H), 3.30(d,J=16.4Hz,1H), 1.53(s,3H);LC-MS(ESI):m / z=545(M+H) +

[0383] Example 133 (2S,3R,5R)-3-(((2-((4S,5R)-2-(2,3-dihydroxyphenyl)-5-methyl-4,5-dihydrooxazole-4-carbonyl)hydrazinecarbonyl)oxy)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0384] The title compound was prepared using a procedure similar to that described in Example 69, except that (4S,5R)-2-(2,3-dihydroxyphenyl)-5-methyl-4,5-dihydrooxazole-4-carbohydrazide was used instead of 3,4-dihydroxybenzohydrazide. 1H NMR (400MHz, DMSO-d6)δ 14.02(br,1H), 10.91(s,1H), 10.32(s,1H), 7.16(t,J=7.5Hz,1H), 6.88-6.77(m, 3H), 5.19(dq,J=8.0, 5.7Hz,1H), 5.11(s,1H), 4.73-4.61(m,2H), 4.50(dd,J=12.5 , 6.0Hz,1H), 4.39(t,J=6.2Hz,2H), 4.25(dd,J=12.4, 6.1Hz,1H), 3.98(d,J=8.1Hz ,1H), 3.55(s,1H), 1.68(d,J=5.7Hz,3H), 1.43(s,3H);LC-MS(ESI):m / z=527(M+H) +

[0385] Example 134 (2S,3R,5R)-3-((((3,4-dihydroxyphenethyl)carbamoyl)oxy)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0386] The title compound was prepared using a similar procedure as described in Example 69, except using 4-(2-aminoethyl)benzene-1,2-diol instead of 3,4-dihydroxybenzohydrazide. 1 H NMR (400MHz, DMSO-d6) δ 14.01(br,1H), 10.59(s,1H), 10.32(s,1H), δ 6.64-6.44(m,3H), 4.74-4.61(m,2H), 4.48(s,1H), 4.39(t,J=6.2Hz,2H), 3.59(s,1H), 3.50-3.34( m,3H), 3.21(dd,J=12.5, 9.2Hz,1H), 2.87(t,J=6.0Hz,2H), 1.43(s,3H);LC-MS(ESI):m / z=429(M+H) +

[0387] Example 135 (2S,3R,5R)-3-(5-(3,4-dihydroxybenzoyl)isoxazol-3-yl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide [ka]

[0388] The title compound was prepared using a procedure similar to that described in Example 101, except using 1-(3,4-bis(benzyloxy)phenyl)prop-2-yn-1-one instead of 4,4'-(((3-chloro-4-ethynyl-1,2-phenylene)bis(oxy))bis(methylene))bis(methoxybenzene). 1 H NMR (400MHz, DMSO)δ 7.72(s,1H), 7.52(dd,J=6.3, 2.0Hz,2H), 6.97(d,J=8.9Hz,1H), 5.43(s,1H),5. 26(s,1H), 3.75(dd,J=16.6, 4.6Hz,2H), 1.94(s,3H);LC-MS(ESI):m / z=423(M+H) +

[0389] Example 136 (2S,3S,5R)-3-((4-((E)-(2-(2-chloro-3,4-dihydroxybenzoyl)hydrazono)methyl)-1H-imidazol-1-yl)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0390] FIG. 19 shows a synthetic scheme for preparing this compound. Step 1. To a solution of benzhydryl (2S,3R,5R)-3-(chloromethyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate (1.5 g, 3.7 mmol) in acetonitrile (15 mL) and H2O (5 mL) was added 1H-pyrrole-3-carbaldehyde (0.35 g, 3.7 mmol) and sodium bicarbonate (0.62 g, 7.4 mmol). The mixture was stirred at room temperature for 10 hours. The solvent was then extracted with ethyl acetate and the residue was evaporated under vacuum to give (2S,3S,5R)-benzhydryl 3-((4-formyl-1H-imidazol-1-yl)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate (1 g, 58.8% yield); LC-MS (ESI): m / z=462

[0391] Step 2. Benzhydryl (2S,3S,5R)-3-((4-formyl-1H-imidazol-1-yl)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate (1 g, 2.2 mmol) in DCM (10 mL) and EtOH (10 mL) was added with 3,4-bis(benzyloxy)-2-chlorobenzohydrazide (0.84 g, 2.2 mmol). The mixture was stirred at room temperature for 6 hours. The solvent was then evaporated under vacuum and the residue was purified by flash chromatography (DCM:MeOH=20:1) to give benzhydryl (2S,3S,5R)-3-((4-((E)-(2-(3,4-bis(benzyloxy)-2-chlorobenzoyl)hydrazono)methyl)-1H-imidazol-1-yl)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate as a white solid (0.85 g, 47.4% yield); LC-MS (ESI): m / z=826

[0392] Step 3. Benzhydryl (2S,3S,5R)-3-((4-((E)-(2-(3,4-bis(benzyloxy)-2-chlorobenzoyl)hydrazono)methyl)-1H-imidazol-1-yl)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate (0.85 g, 1.0 mmol) in acetic acid (10 mL), acetone (2 mL) and H2O (2 mL) was cooled to 0° C. and potassium permanganate (0.32 g, 2.0 mmol) was added slowly. The mixture was stirred at room temperature for 2 hours. The reaction was then quenched by the addition of sodium metabisulfite solution and extracted with ethyl acetate. The solvent was evaporated under vacuum and the residue was purified by flash chromatography (DCM:MeOH=20:1) to give benzhydryl (2S,3S,5R)-3-((4-((E)-(2-(3,4-bis(benzyloxy)-2-chlorobenzoyl)hydrazono)methyl)-1H-imidazol-1-yl)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate 4,4-dioxide as a white solid (0.3 g, 34.9% yield); LC-MS (ESI): m / z=858.

[0393] Step 4. Benzhydryl (2S,3S,5R)-3-((4-((E)-(2-(3,4-bis(benzyloxy)-2-chlorobenzoyl)hydrazono)methyl)-1H-imidazol-1-yl)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate 4,4-dioxide (0.3 g, 0.35 mmol) was dissolved in 10 mL of THF, Pd / C (10%, 100 mg) was added, and the solution was stirred under a hydrogen-filled balloon for 8 h. Palladium was removed by filtration, then the solvent was evaporated under vacuum, and the residue was purified by column chromatography (silica gel, DCM:MeOH=20:1) to give the title compound as a white solid (85 mg, 47.5% yield). 1H NMR (400MHz, DMSO)δ 11.58(s,1H), 10.14(s,1H), 9.34(s,1H), 8.31(s,1H), 7.82(s,1H), 7.3 9(s,1H), 7.25(dd,J=19.7, 7.0Hz,1H), 6.87(d,J=8.2Hz,1H), 6.82-6.77 (m,1H), 5.16(d,J=3.2Hz,1H), 5.09(d,J=15.4Hz,1H), 4.98(d,J=15.5Hz,1H), 4.62(s,1H), 3.32(s,2H), 1.45(s,3H);LC-MS(ESI):m / z=512(M+H) +

[0394] Example 137 (2S,3R,5R)-3-((E)-(((1-(2-chloro-3,4-dihydroxybenzoyl)piperidin-4-yl)oxy)imino)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0395] The title compound was prepared using a similar procedure as described in Example 119, except using (4-(aminooxy)piperidin-1-yl)(2-chloro-3,4-dihydroxyphenyl)methanone instead of N-(4-(aminooxy)phenyl)-2-chloro-3,4-dihydroxybenzamide. 1H NMR (400MHz, DMSO-d6) δ 14.01(br,1H), 10.58(s,1H), 10.32(s,1H), δ 7.48(s,1H), 7.16(d,J=7.5Hz,1H), 6.65(d,J=7.5Hz,1H), 6.06(s,1H), 4.7 0(t,J=9.3Hz,1H), 4.56-4.47(m,1H), 3.66(dt,J=12.4, 5.3Hz,2H), 3.50-3. 35(m,3H), 3.21(dd,J=12.4, 9.3Hz,1H), 2.39(dqd,J=12.8, 5.4, 2.2Hz,2H), 1.82(dqd,J=12.9, 5.4, 2.2Hz,2H), 1.56(s,3H);LC-MS(ESI):m / z=516(M+H) +

[0396] Example 138 (2S,3R,5R)-3-((E)-(((1-(2-chloro-3,4-dihydroxybenzoyl)azetidin-3-yl)oxy)imino)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide: [ka]

[0397] The title compound was prepared using a procedure similar to that described in Example 119, except using (3-(aminooxy)azetidin-1-yl)(2-chloro-3,4-dihydroxyphenyl)methanone instead of N-(4-(aminooxy)phenyl)-2-chloro-3,4-dihydroxybenzamide. 1 H NMR (400MHz, DMSO-d6)δ 14.01(br,1H), 10.58(s,1H), 10.32(s,1H), 7.49(s,1H), 7.27(s,1H), 6.66(s,1H), 5.41(s,1H), 4.70(s,1H), 4.59(s ,1H), 4.20-4.04(m,2H), 3.95-3.80(m,2H), 3.46(s,1H), 3.21(s,1H), 1.58-1.54(m,3H);LC-MS(ESI):m / z=488(M+H)+

[0398] Example 139 biological activity MIC measurement

[0399] Minimum inhibitory concentrations (MICs) were determined according to the broth microdilution method recommended by the Clinical and Laboratory Standards Institute (CLSI) with minor modifications. For all MIC studies, iron-deficient cation-adjusted Mueller-Hinton broth (supplemented with 2,2-dipyridyl at 160 μM) was used to form iron complexes and thus induce the iron uptake system. The ESKAPE panel of bacterial strains (E. faecium ATCC 700221, S. aureus ATCC 29213, K. pneumoniae ATCC 43816, A. baumannii ATCC 19606, P. aeruginosa ATCC 27853, and Escherichia coli ATCC 25922) were initially obtained from the American Type Culture Collection (ATCC) and used for compound MIC determination. The bacterial inoculum size for the study was approximately 5x10 5 CFU / well. The MIC is defined as the lowest concentration after 18-20 hours of incubation at 37°C in the presence of 5% CO2 that prevents visible bacterial growth. The results are summarized in Tables 2 and 3 below.

[0400] Table 2. MICs (μg / mL) of selected and comparative compounds against ESKAPE bacterial strains. [Table 19] [Table 20]

[0401] Table 3. MICs (μg / mL) of selected compounds alone and in combination with antibiotics against clinical isolates of Acinetobacter baumannii [Table 21] [Table 22] NT: Not tested

[0402] β-lactamase inhibitor activity assay

[0403] Hydrolytic inactivation of β-lactam antibiotics by β-lactamases is the most widespread drug resistance mechanism among Gram-negative pathogens and represents the greatest clinical challenge. Based on amino acid sequence, β-lactamases are classified into four classes (Ambler classification), of which A, C, and D include serine hydrolases and B includes metallo-β-lactamases. In addition to selected derivatives disclosed herein (identified in conjunction with the Example number), the IC of six control β-lactam or β-lactamase inhibitors was also reported. 50 was measured against seven representative β-lactamases of different classes in a standard spectrophotometric assay of nitrocefin hydrolysis. The results are summarized in Table 4 below. The assay is performed in 384-well plates. Seven recombinant β-lactamases AmpC_AB (from A. Baumannii), AmpC_PA (from P. aeruginosa), KPC-2, NDM-1, IMP-1, VIM-1 and OXA 24 / 40 are expressed and purified. The reaction buffer for class A, C and D enzymes is 100 mM Na2HPO4-KH2PO4 (pH 7.1) + 0.005% Tween-20, and for class B enzymes, 10 μM ZnSO4 is added. Control compounds include clavulanate, sulbactam, tazobactam, avibactam, relebactam and didebactam. A 50 μL reaction solution consisting of 2 pM β-lactamase, 200 μM nitrocefin and a series of 3-fold dilutions of test or control compounds is added to a 384 plate in the Cybio SELMA system and incubated for 2 hours at 25° C. in the dark. OD 490The plate was read on an MC SpectraMax Plus 384 plate reader. The % inhibition at each concentration was calculated as [1-(compound OD-nonenzyme average OD) / (enzyme average OD-nonenzyme average OD)] x 100% and the IC 50 The IC of avibactam and relebactam in the assay is calculated using XLfit. 50 are consistent with previous data, thus validating the assay method. Results show that the test compounds exhibited IC values ​​in the range of 409-65,160 nM against class C β-lactamases AmpC_AB, AmpC_PA, and class D β-lactamases OXA24 / 40. 50 The results show that the β-lactamases have strong inhibitory activity against class A and B β-lactamases. Except for Example 70 which shows weak activity against class A KPC-2 and Example 7 which shows weak activity against class B VIM-1, the other Examples show no detectable activity against class A and B β-lactamases.

[0404] Table 4. IC of illustrative compounds against various β-lactamases 50 (nM) [Table 23]

Claims

1. formula: 【Chemistry 1】 [In the formula, R １ is hydrogen; Y is independently -S-, -SO-, or -SO ２ - selected from; L is (C １ -C ８ ) alkylene, containing 1 to 3 heteroatoms (C ３ -C ８ ) cycloalkylene, (C 6 or C 10 ) arylene, (C 5 or C 6 ) heteroarylene containing 1 to 3 heteroatoms, (C ３ -C ８ ) heterocycloalkylene, -C(=O)-, -O-, -S(O) ｎ -(where n is 0, 1, or 2), -N(R ２ ) -, -C(R ３ ) = C(R ４ )-, and -C=N-, Here, R ２ , R ３ and R ４ is hydrogen, (C １ -C ８ ) alkyl, (C ３ -C ８ ) cycloalkyl, (C １ -C ８ ) alkyloxyl, (C 6 or C 10 ) aryl, (C 5 or C 6 ) heteroaryl containing 1 to 3 heteroatoms, and (C ３ -C ８ ) heterocycloalkyl; or R ３ and R ４ together form a bond; and Z is 【Chemistry 2】 and wherein the iron chelating moiety is selected from Here, R ５ , R ６ and R ７ are independently hydrogen, hydroxyl, halogen, nitrile, nitro, amino, CF ３ , O.C.F. ３ , (C 1 -C 6 )alkyl, (C 1 -C 3 )alkylamino, or (C 1 -C 6 )alkoxy; or R ５ , R ６ and R ７ Two of these combine together to form a 5-8 membered ring. or a stereoisomer, pharma- ceutically acceptable salt, solvate, or deuterium exchanged compound thereof.

2. 2. The compound of claim 1, wherein L contains a carbon or nitrogen atom and is further substituted with 1 to 3 substituents.

3. R ５ , R ６ and R ７ The compound according to claim 1, wherein the 5-8 membered ring formed by two of

4. Y is -SO ２ The compound according to claim 1, wherein

5. Lto-CH=N-N(R ２ )-X-、-EH ２ O (O) - N (R) ２ )-X-、-CH=N-O-X-、-CH ２ *C(O)-X-、-CH ２ N(R ２ )-+-、 【Chemistry 3】 where X is selected from (C １ -C ８ ) alkylene, (C ３ -C ８ ) cycloalkylene, (C ３ -C ８ ) heterocycloalkylene, (C 6 or C 10 ) arylene, (C 5 or C 6 ) heteroarylene containing 1 to 3 heteroatoms, —O—, —N(R ２ )-, and -C(O)-, or a combination of 2 to 5 groups selected from R ２ is hydrogen, (C １ -C ８ ) alkyl, (C ３ -C ８ ) cycloalkyl, (C １ -C ８ ) alkyloxyl, (C 6 or C 10 ) aryl, (C 5 or C 6 ) heteroaryl containing 1 to 3 heteroatoms, or (C ３ -C ８ ) heterocycloalkyl; The compound of claim 1.

6. L is (C ３ -C ８ ) heterocycloalkylene, where (C ３ -C ８ 2. The compound of claim 1 , wherein the heterocycloalkylene is unsubstituted.

7. Z is: 【Chemistry 4】 【Chemistry 5】 The compound of claim 1 selected from:

8. 13. A pharmaceutical composition comprising a pharma- ceutical effective amount of a compound of claim 1 in combination with a pharma- ceutical acceptable carrier.

9. 9. The pharmaceutical composition of claim 8, further comprising one or more additional antibacterial agents.

10. 13. A pharmaceutical composition for treating or preventing a microbial infection comprising a pharma- ceutical effective amount of a compound of claim 1 in combination with a pharma- ceutical acceptable carrier.

11. 11. The pharmaceutical composition of claim 10, further comprising one or more additional antibacterial agents.

12. 13. Use of a compound according to claim 1 in the manufacture of a medicament for the treatment or prevention of a microbial infection.

13. (2S,3R,5R)-3-((E)-(2-(2-chloro-4,5-dihydroxybenzoyl)hydrazono)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide; (2S,3R,5R)-3-methyl-7-oxo-3-((E)-(2-(2,3,4-trihydroxybenzoyl)hydrazono)methyl)-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide; (2S,3R,5R)-3-((E)-(2-(2-chloro-3,4-dihydroxybenzoyl)-2-methylhydrazono)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide; (2S,3R,5R)-3-((E)-(2-(2,5-dichloro-3,4-dihydroxybenzoyl)hydrazono)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide; (2S,3R,5R)-3-((E)-(2-(3,4-dihydroxybenzoyl)hydrazono)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide; (2S,3R,5R)-3-methyl-7-oxo-3-((E)-(2-(3,4,5-trihydroxybenzoyl)hydrazono)methyl)-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide; (2S,3R,5R)-3-((E)-(2-(3,4-dihydroxybenzoyl)-2-methylhydrazono)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide; (2S,3R,5R)-3-((E)-(2-(2-bromo-3,4-dihydroxybenzoyl)hydrazono)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide; (2S,3R,5R)-3-methyl-7-oxo-3-((E)-(2-(2,3,6-trichloro-4,5-dihydroxybenzoyl)hydrazono)methyl)-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide; (2S,3R,5R)-3-((E)-(2-(2,6-dichloro-3,4-dihydroxybenzoyl)hydrazono)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide; (2S,3R,5R)-3-((E)-(2-(2-fluoro-3,4-dihydroxybenzoyl)hydrazono)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide; (2S,3R,5R)-3-((E)-(2-(3,4-dihydroxy-2-methylbenzoyl)hydrazono)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide; (2S,3R,5R)-3-((E)-(2-(2-(3,4-dihydroxyphenyl)acetyl)hydrazono)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide; (2S,3R,5R)-3-((E)-(2-((R)-2-((tert-butoxycarbonyl)amino)-3-(3,4-dihydroxyphenyl)propanoyl)hydrazono)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide; (2S,3R,5R)-3-((E)-(2-(3-chloro-4,5-dihydroxybenzoyl)hydrazono)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide; (2S,3R,5R)-3-((E)-(2-(2-chloro-3,4-dihydroxybenzoyl)hydrazono)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide; (2S,3R,5R)-3-((E)-(2-(3-(3,4-dihydroxyphenyl)propanoyl)hydrazono)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide; (2S,3R,5R)-3-((E)-(2-(2,3-dihydroxybenzoyl)hydrazono)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide; (2S,3R,5R)-3-((E)-(2-(1-(2-chloro-3,4-dihydroxybenzoyl)pyrrolidine-3-carbonyl)hydrazono)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide; (2S,3R,5R)-3-((E)-(2-(1-(2-chloro-3,4-dihydroxybenzoyl)azetidine-3-carbonyl)hydrazono)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide; (2S,3R,5R)-3-((E)-(2-(1-(2-chloro-3,4-dihydroxybenzoyl)pyrrolidine-2-carbonyl)hydrazono)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide; (2S,3R,5R)-3-((E)-(2-(5-(3,4-dihydroxybenzamido)picolinoyl)hydrazono)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide; (2S,3R,5R)-3-((E)-(2-(1-(2-chloro-3,4-dihydroxybenzoyl)piperidine-4-carbonyl)hydrazono)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide; (2S,3R,5R)-3-((E)-(2-(2-(2-chloro-3,4-dihydroxybenzamido)-3-hydroxypropanoyl)hydrazono)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide; (2S,3R,5R)-3-((E)-(2-(2-(2-chloro-3,4-dihydroxybenzamido)-3-phenylpropanoyl)hydrazono)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide; (2S,3R,5R)-3-((E)-(2-(4-((2-chloro-3,4-dihydroxybenzamido)methyl)benzoyl)hydrazono)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide; (2S,3R,5R)-3-((E)-(2-(4-((3,4-dihydroxybenzamido)methyl)benzoyl)hydrazono)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide; ((2S,3R,5R)-3-((E)-(2-(2-(3,4-dihydroxybenzamido)-3-methylbutanoyl)hydrazono)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide; (2S,3R,5R)-3-((E)-(2-(2-(2-chloro-3,4-dihydroxybenzamido)-3-methylbutanoyl)hydrazono)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide; (2S,3R,5R)-3-((E)-(2-(1-(2-chloro-3,4-dihydroxybenzoyl)piperidine-3-carbonyl)hydrazono)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide; (2S,3R,5R)-3-((E)-(2-(2-(3,4-dihydroxybenzamido)-3-hydroxypropanoyl)hydrazono)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide; (2S,3R,5R)-3-((E)-(2-(2-(3,4-dihydroxybenzamido)-3-phenylpropanoyl)hydrazono)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide; (2S,3R,5R)-3-((E)-(2-(1-(3,4-dihydroxybenzamido)cyclopropanecarbonyl)hydrazono)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide; (2S,3R,5R)-3-((E)-(2-(1-(2-chloro-3,4-dihydroxybenzamido)cyclopropanecarbonyl)hydrazono)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide; (2S,3R,5R)-3-((E)-(2-(4-((3,4-dihydroxybenzoyl)oxy)benzoyl)hydrazono)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide; (2S,3R,5R)-3-((E)-(2-(2-((tert-butoxycarbonyl)amino)-3-((2-chloro-3,4-dihydroxybenzoyl)oxy)propanoyl)hydrazono)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide; (2S,3R,5R)-3-((E)-(2-(3',4'-dihydroxy-[1,1'-biphenyl]-4-carbonyl)hydrazono)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide; (2S,3R,5R)-3-((E)-(2-(4-((2-chloro-3,4-dihydroxybenzoyl)oxy)benzoyl)hydrazono)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide; (2S,3R,5R)-3-((E)-(2-(5-(2-chloro-3,4-dihydroxybenzamido)picolinoyl)hydrazono)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide; (2S,3R,5R)-3-((E)-(2-(2-(2-chloro-3,4-dihydroxybenzamido)acetyl)hydrazono)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide; (2S,3R,5R)-3-((E)-(2-(3-(2-chloro-3,4-dihydroxybenzamido)propanoyl)hydrazono)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide; (2S,3R,5R)-3-((E)-(2-(6-(2-chloro-3,4-dihydroxybenzamido)hexanoyl)hydrazono)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide; (2S,3R,5R)-3-((E)-(2-((S)-2-(2-chloro-3,4-dihydroxybenzamido)propanoyl)hydrazono)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide; (2S,3R,5R)-3-((E)-(2-(4-(2-chloro-3,4-dihydroxybenzamido)butanoyl)hydrazono)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide; (2S,3R,5R)-3-((E)-(2-(2-(3,4-dihydroxybenzamido)acetyl)hydrazono)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide; (2S,3R,5R)-3-((E)-(2-((S)-2-(3,4-dihydroxybenzamido)propanoyl)hydrazono)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide; (2S,3R,5R)-3-((E)-(2-(4-(3,4-dihydroxybenzamido)butanoyl)hydrazono)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide; (2S,3R,5R)-3-((E)-(2-(3-(3,4-dihydroxybenzamido)propanoyl)hydrazono)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide; (2S,3R,5R)-3-((E)-(2-(6-(3,4-dihydroxybenzamido)hexanoyl)hydrazono)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide; (2S,3R,5R)-3-(((2-(3,4-dihydroxybenzoyl)hydrazinecarbonyl)oxy)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide; (2S,3R,5R)-3-(((2-(2-chloro-3,4-dihydroxybenzoyl)hydrazinecarbonyl)oxy)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide; (2S,3R,5R)-3-(((2-(2-(3,4-dihydroxyphenyl)-2-oxoethyl)hydrazinecarbonyl)oxy)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide; (2S,3R,5R)-3-(((2-(2,3-dihydroxybenzoyl)hydrazinecarbonyl)oxy)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide; (2S,3R,5R)-3-methyl-7-oxo-3-(((2-(3,4,5-trihydroxybenzoyl)hydrazinecarbonyl)oxy)methyl)-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide; (2S,3R,5R)-3-(((2-(3,4-dihydroxybenzoyl)-1-methylhydrazinecarbonyl)oxy)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide; (2S,3R,5R)-3-(((2-(2-chloro-4,5-dihydroxybenzoyl)hydrazinecarbonyl)oxy)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide; (2S,3R,5R)-3-(((2-(2-chloro-3,4-dihydroxybenzoyl)-1-methylhydrazinecarbonyl)oxy)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide; (2S,3R,5R)-3-(((2-(3,4-dihydroxybenzoyl)-2-methylhydrazinecarbonyl)oxy)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide; (2S,3R,5R)-3-methyl-7-oxo-3-(((2-(2,3,4-trihydroxybenzoyl)hydrazinecarbonyl)oxy)methyl)-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide; (2S,3R,5R)-3-(((2-(2,6-dichloro-3,4-dihydroxybenzoyl)hydrazinecarbonyl)oxy)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide; (2S,3R,5R)-3-(((2-(2,5-dichloro-3,4-dihydroxybenzoyl)hydrazinecarbonyl)oxy)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide; (2S,3R,5R)-3-(((2-(2-fluoro-3,4-dihydroxybenzoyl)hydrazinecarbonyl)oxy)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide; (2S,3R,5R)-3-(((2-(3-(3,4-dihydroxyphenyl)-3-oxopropyl)hydrazinecarbonyl)oxy)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide; (2S,3R,5R)-3-(((2-(2-chloro-4,5-dihydroxybenzoyl)hydrazinecarbonyl)oxy)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide; (2S,3R,5R)-3-((((E)-2-(3,4-dihydroxybenzylidene)hydrazinecarbonyl)oxy)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide; (2S,3R,5R)-3-(((2-(3-chloro-4,5-dihydroxybenzoyl)hydrazinecarbonyl)oxy)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide; (2S,3R,5R)-3-(((2-(2-(3,4-dihydroxybenzamido)acetyl)hydrazinecarbonyl)oxy)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide; (2S,3R,5R)-3-(((3-(3,4-dihydroxybenzamido)pyrrolidine-1-carbonyl)oxy)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide; (2S,3R,5R)-3-(((4-(3,4-dihydroxybenzoyl)piperazine-1-carbonyl)oxy)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide; (2S,3R,5R)-3-(((2-(2-(2-chloro-3,4-dihydroxybenzamido)acetyl)hydrazinecarbonyl)oxy)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide; (2S,3R,5R)-3-((((2-(2-chloro-3,4-dihydroxybenzamido)ethyl)carbamoyl)oxy)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide; (2S,3R,5R)-3-(((4-(3,4-dihydroxybenzamido)piperidine-1-carbonyl)oxy)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide; (2S,3R,5R)-3-((((1-(3,4-dihydroxybenzoyl)pyrrolidin-3-yl)carbamoyl)oxy)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide; (2S,3R,5R)-3-(((3-(3,4-dihydroxybenzamido)azetidine-1-carbonyl)oxy)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide; (2S,3R,5R)-3-(5-(2-(2-chloro-3,4-dihydroxyphenyl)-2-oxoethyl)isoxazol-3-yl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide; (2S,3R,5R)-3-(5-(2-(3,4-dihydroxyphenyl)-2-oxoethyl)isoxazol-3-yl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide; (2S,3R,5R)-3-(5-(2-chloro-3,4-dihydroxyphenyl)isoxazol-3-yl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide; (2S,3R,5R)-3-(5-(2-(2,5-dichloro-3,4-dihydroxyphenyl)-2-oxoethyl)isoxazol-3-yl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide; (2S,3R,5R)-3-(5-(3,4-dihydroxyphenyl)isoxazol-3-yl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide; (2S,3R,5R)-3-(5-(2-((2-chloro-3,4-dihydroxybenzoyl)oxy)ethyl)isoxazol-3-yl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide; (2S,3R,5R)-3-(5-(2,5-dichloro-3,4-dihydroxyphenyl)isoxazol-3-yl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide; (2S,3R,5R)-3-(5-(2-((3,4-dihydroxybenzoyl)oxy)ethyl)isoxazol-3-yl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide; (2S,3R,5R)-3-(5-(2-((2-chloro-3,4-dihydroxybenzoyl)oxy)ethyl)-4,5-dihydroisoxazol-3-yl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide; (2S,3R,5R)-3-(5-(2-chloro-3,4-dihydroxyphenyl)-4,5-dihydroisoxazol-3-yl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide; (2S,3R,5R)-3-(5-((2,5-dichloro-3,4-dihydroxybenzamido)methyl)-4,5-dihydroisoxazol-3-yl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide; (2S,3R,5R)-3-(5-(2-((3,4-dihydroxybenzoyl)oxy)ethyl)-4,5-dihydroisoxazol-3-yl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide; (2S,3R,5R)-3-(5-((2-chloro-3,4-dihydroxybenzamido)methyl)-4,5-dihydroisoxazol-3-yl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide; (2S,3R,5R)-3-(5-(3,4-dihydroxybenzoyl)isoxazol-3-yl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide; (2S,3R,5R)-3-(((3,4-dihydroxybenzoyl)oxy)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide; (2S,3R,5R)-3-(((2-chloro-3,4-dihydroxybenzoyl)oxy)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide; (2S,3S,5R)-3-(((3,4-dihydroxyphenyl)amino)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide; (2S,3R,5R)-3-((E)-((2-(2-chloro-3,4-dihydroxybenzamido)ethoxy)imino)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide; (2S,3R,5R)-3-((E)-((4-(2-chloro-3,4-dihydroxybenzamido)phenoxy)imino)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide; (2S,3R,5R)-3-(5-(2-chloro-3,4-dihydroxybenzoyl)isoxazol-3-yl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide; (2S,3R,5R)-3-((E)-(2-(2-bromo-4,5-dihydroxybenzoyl)hydrazono)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide; (2S,3R,5R)-3-((E)-(2-(3-(3,4-dihydroxyphenyl)-5-methylisoxazole-4-carbonyl)hydrazono)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide; (2S,3R,5R)-3-((E)-(2-(3-(2-chloro-3,4-dihydroxyphenyl)isoxazole-5-carbonyl)hydrazono)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide; (2S,3R,5R)-3-((E)-(2-(3-(3,4-dihydroxyphenyl)isoxazole-5-carbonyl)hydrazono)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide; (2S,3R,5R)-3-((E)-(2-((4S,5R)-2-(2,3-dihydroxyphenyl)-5-methyl-4,5-dihydrooxazole-4-carbonyl)hydrazono)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide; (2S,3R,5R)-3-((E)-(2-((4S,5R)-2-(3,4-dihydroxyphenyl)-5-methyl-4,5-dihydrooxazole-4-carbonyl)hydrazono)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide; (2S,3R,5R)-3-(((2-(3-(2,3-dihydroxyphenyl)isoxazole-5-carbonyl)hydrazinecarbonyl)oxy)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide; (2S,3R,5R)-3-(((2-(3-(2,3-dihydroxyphenyl)-4,5-dihydroisoxazole-5-carbonyl)hydrazinecarbonyl)oxy)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide; (2S,3R,5R)-3-(((4-(2-chloro-3,4-dihydroxybenzoyl)piperazine-1-carbonyl)oxy)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide; (2S,3R,5R)-3-(((3-(2-chloro-3,4-dihydroxybenzamido)azetidine-1-carbonyl)oxy)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide; (2S,3R,5R)-3-(((2-(3-(2-chloro-3,4-dihydroxyphenyl)-4,5-dihydroisoxazole-5-carbonyl)hydrazine-1-carbonyl)oxy)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide; (2S,3R,5R)-3-(((2-(3-(2-chloro-3,4-dihydroxyphenyl)-4,5-dihydroisoxazole-5-carbonyl)hydrazinecarbonyl)oxy)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide; (2S,3R,5R)-3-(((2-((4S,5R)-2-(2,3-dihydroxyphenyl)-5-methyl-4,5-dihydrooxazole-4-carbonyl)hydrazinecarbonyl)oxy)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide; (2S,3R,5R)-3-((((3,4-dihydroxyphenethyl)carbamoyl)oxy)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide; (2S,3R,5R)-3-(5-(3,4-dihydroxybenzoyl)isoxazol-3-yl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide; (2S,3S,5R)-3-((4-((E)-(2-(2-chloro-3,4-dihydroxybenzoyl)hydrazono)methyl)-1H-imidazol-1-yl)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide; (2S,3R,5R)-3-((E)-(((1-(2-chloro-3,4-dihydroxybenzoyl)piperidin-4-yl)oxy)amino)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide; and (2S,3R,5R)-3-((E)-(((1-(2-chloro-3,4-dihydroxybenzoyl)azetidin-3-yl)oxy)imino)methyl)-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide A compound selected from the group consisting of

14. 14. A pharmaceutical composition comprising a pharma- ceutical effective amount of a compound of claim 13 in combination with a pharma- ceutical acceptable carrier.

15. 15. The pharmaceutical composition of claim 14, further comprising one or more additional antibacterial agents.

16. 14. A pharmaceutical composition for treating or preventing a microbial infection comprising a pharma- ceutical effective amount of a compound of claim 13 in combination with a pharma- ceutical acceptable carrier.

17. 17. The pharmaceutical composition of claim 16, further comprising one or more additional antibacterial agents.

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