GLUCOCORTICOIDREZEPTORAGONISTEN

Description

[0001] The present disclosure provides compounds that are glucocorticoid receptor agonists and are useful for the treatment of autoimmune and inflammatory diseases, such as atopic dermatitis, inflammatory bowel disease, systemic lupus erythematosus, lupus nephritis, and rheumatoid arthritis, processes for preparing these compounds, pharmaceutical compositions comprising these compounds, and methods of using these compounds and compositions are also provided.

[0002] Atopic dermatitis is a chronic, pruritic relapsing and remitting inflammatory skin disease that occurs frequently in children, but also affects many adults. Current treatments of atopic dermatitis include light therapy, topical creams containing corticosteroids or calcineurin inhibitors, or a subcutaneous injectable biologic known as dupilumab. In spite of progress made in treating atopic dermatitis, there remains a significant need for new compounds to treat atopic dermatitis and other inflammatory and autoimmune diseases.

[0003] WO2017 / 210471 discloses certain glucocorticoid receptor agonists and immunoconjugates thereof useful for treating autoimmune or inflammatory diseases. WO2018 / 089373 discloses novel steroids, protein conjugates thereof, and methods for treating diseases, disorders, and conditions comprising administering the steroids and conjugates. WO2019 / 106608 and WO2019 / 106609 disclose certain glucocorticoid receptor agonists and immunoconjugates thereof.

[0004] The present invention provides certain novel compounds which are glucocorticoid receptor agonists. The present invention further provides certain novel compounds which are prodrugs of glucocorticoid receptor agonists. In addition, the present invention provides certain novel compounds which are glucocorticoid receptor agonists useful in the treatment of autoimmune and inflammatory diseases such as atopic dermatitis, inflammatory bowel disease, rheumatoid arthritis, systemic lupus erythematosus, and lupus nephritis.

[0005] Accordingly, in one embodiment, the invention provides a compound of Formula I: wherein R is H or R 1< is H, halogen, CN, C1-C3 alkyl, C3-C6 cycloalkyl, C1-C3 alkoxy, C2-C3 alkenyl, OCF 3 , R 2< is H, halogen, C1-C3 alkyl, C1-C3 alkoxy, or C2-C3 alkenyl; R 3< is NH 2 , or CH 2 NH 2 ; and X is O, OCH 2 , OCH 2 CH 2 , CH 2 O, SCH 2 , CH 2 S, CH 2 , NHCH 2 , CH 2 NH, N(CH 3 )CH 2 , CH 2 CH 2 , C≡C, or a bond, wherein X is connected to phenyl ring A at the ortho or the meta position, or a pharmaceutically acceptable salt thereof, and wherein the compound is not: or Certain compounds disclosed in EP4393937 (a European patent application derived from WO2023025248) are hereby disclaimed from the scope of the present invention. EP4393937 discloses steroid compounds and conjugates thereof and was first published after the filing date of the present application.

[0006] In one embodiment, the invention provides a compound of Formula Ia: wherein R is H or R 1< is H, halogen, C1-C3 alkyl, C3-C6 cycloalkyl, C1-C3 alkoxy, C2-C3 alkenyl, OCF 3 , R 2< is H, halogen, C1-C3 alkyl, C1-C3 alkoxy, or C2-C3 alkenyl; R 3< is NH 2 , or CH 2 NH 2 ; and X is O, OCH 2 , OCH 2 CH 2 , CH 2 O, SCH 2 , CH 2 S, CH 2 , NHCH 2 , CH 2 NH, N(CH 3 )CH 2 , CH 2 CH 2 , C≡C, or a bond, wherein X is connected to phenyl ring A at the ortho or the meta position, or a pharmaceutically acceptable salt thereof.

[0007] In one embodiment, the invention provides a compound of Formula Ib: wherein R is H or R 1< is H, halogen, C1-C3 alkyl, C3-C6 cycloalkyl, C1-C3 alkoxy, C2-C3 alkenyl, OCF 3 , R 2< is H, halogen, C1-C3 alkyl, C1-C3 alkoxy, or C2-C3 alkenyl; R 3< is NH 2 , or CH 2 NH 2 ; and X is O, OCH 2 , OCH 2 CH 2 , CH 2 O, SCH 2 , CH 2 S, CH 2 , NHCH 2 , CH 2 NH, N(CH 3 )CH 2 , CH 2 CH 2 , C≡C, or a bond, wherein X is connected to phenyl ring A at the ortho or the meta position, or a pharmaceutically acceptable salt thereof.

[0008] In one embodiment, the invention provides a compound of Formula Ic: wherein R is H or R 1< is H, halogen, C1-C3 alkyl, C3-C6 cycloalkyl, C1-C3 alkoxy, C2-C3 alkenyl, OCF 3 , R 2< is H, halogen, C1-C3 alkyl, C1-C3 alkoxy, or C2-C3 alkenyl; R 3< is NH 2 , or CH 2 NH 2 ; and X is O, OCH 2 , OCH 2 CH 2 , CH 2 O, SCH 2 , CH 2 S, CH 2 , NHCH 2 , CH 2 NH, N(CH 3 )CH 2 , CH 2 CH 2 , C≡C, or a bond, wherein X is connected to phenyl ring A at the ortho or the meta position, or a pharmaceutically acceptable salt thereof.

[0009] In an embodiment, the invention provides a compound of Formula Ib(i): or a pharmaceutically acceptable salt thereof.

[0010] In an embodiment, the invention provides a compound of Formula Ic(i): or a pharmaceutically acceptable salt thereof.

[0011] In an embodiment, the invention provides a compound of Formula Ib(ii): or a pharmaceutically acceptable salt thereof.

[0012] In an embodiment, the invention provides a compound of Formula Ic(ii): or a pharmaceutically acceptable salt thereof.

[0013] In an embodiment, the invention provides a compound of Formula Ib(iii): or a pharmaceutically acceptable salt thereof.

[0014] In an embodiment, the invention provides a compound of Formula Ic(iii): or a pharmaceutically acceptable salt thereof.

[0015] In one embodiment, the invention provides a compound of Formula II: wherein R is H or and R 1< is -CH 3 or -OCH 3 , or a pharmaceutically acceptable salt thereof.

[0016] In a particular embodiment, the invention provides a compound of Formula IIa: wherein R is H or and R 1< is -CH 3 or -OCH 3 , or a pharmaceutically acceptable salt thereof.

[0017] In a particular embodiment, the invention provides a compound of Formula IIb: wherein R is H or and R 1< is -CH 3 or -OCH 3 , or a pharmaceutically acceptable salt thereof.

[0018] In a particular embodiment, the invention provides a compound of Formula IIc: wherein R is H or and R 1< is -CH 3 or -OCH 3 , or a pharmaceutically acceptable salt thereof.

[0019] In an embodiment, the invention provides a compound of Formula III: wherein R is H or or a pharmaceutically acceptable salt thereof.

[0020] In a particular embodiment, the invention provides a compound of Formula IIIa: wherein R is H or or a pharmaceutically acceptable salt thereof.

[0021] In a particular embodiment, the invention provides a compound of Formula IIIb: wherein R is H or or a pharmaceutically acceptable salt thereof.

[0022] In a particular embodiment, the invention provides a compound of Formula IIIc: wherein R is H or or a pharmaceutically acceptable salt thereof.

[0023] In an embodiment, R is H.

[0024] In an embodiment, R is

[0025] In an embodiment, R 1< is CH 3 .

[0026] In an embodiment, R 1< is H.

[0027] In an embodiment, R 1< is OCH 3 .

[0028] In an embodiment, R 1< is F.

[0029] In an embodiment, R 2< is H.

[0030] In an embodiment, R 2< is CH 3 .

[0031] In an embodiment, R 2< is F.

[0032] In an embodiment, R 2< is OCH 3 .

[0033] In an embodiment, X is O.

[0034] In an embodiment, X is OCH 2 .

[0035] In an embodiment, X is SCH 2 .

[0036] In an embodiment, X is CH 2 .

[0037] In an embodiment, X is a bond.

[0038] In an embodiment, R is H, R 1< is CH 3 , R 2< is F, and X is OCH 2 .

[0039] In an embodiment, R is H, R 1< is OCH 3 , R 2< is F, and X is OCH 2 .

[0040] In an embodiment, X is connected to phenyl ring A at the meta position.

[0041] In an embodiment, X is connected to phenyl ring A at the ortho position.

[0042] Any references to methods of treatment in the subsequent paragraphs of this description are to be interpreted as references to the compounds, pharmaceutical compositions and medicaments of the present invention for use in a method of treatment of a human or animal body by therapy or for diagnosis.

[0043] In an embodiment, the present invention also discloses a method of treating an inflammatory disease in a patient in need of such treatment, comprising administering to the patient an effective amount of a compound of Formula I, or a pharmaceutically acceptable salt thereof. In an embodiment, the present invention also discloses a method of treating atopic dermatitis in a patient in need of such treatment, comprising administering to the patient an effective amount of a compound of Formula I, or a pharmaceutically acceptable salt thereof. In an embodiment, the present invention further discloses a method of treating inflammatory bowel disease in a patient in need of such treatment, comprising administering to the patient an effective amount of a compound of Formula I, or a pharmaceutically acceptable salt thereof. In an embodiment, the present invention further discloses a method of treating rheumatoid arthritis in a patient in need of such treatment, comprising administering to the patient an effective amount of a compound of Formula I, or a pharmaceutically acceptable salt thereof. In an embodiment, the present invention also discloses a method of treating systemic lupus erythematosus in a patient in need of such treatment, comprising administering to the patient an effective amount of a compound of Formula I, or a pharmaceutically acceptable salt thereof. In an embodiment, the present invention also discloses a method of treating lupus nephritis in a patient in need of such treatment, comprising administering to the patient an effective amount of a compound of Formula I, or a pharmaceutically acceptable salt thereof.

[0044] In an embodiment, the present invention further provides a compound of Formula I, or a pharmaceutically acceptable salt thereof for use in therapy. In an embodiment, the present invention provides a compound of Formula I, or a pharmaceutically acceptable salt thereof for use in treating an inflammatory disease. In an embodiment, the present invention provides a compound of Formula I, or a pharmaceutically acceptable salt thereof, for use in treating atopic dermatitis. In an embodiment, the present invention provides a compound of Formula I, or a pharmaceutically acceptable salt thereof, for use in treating rheumatoid arthritis. In an embodiment, the present invention provides a compound of Formula I, or a pharmaceutically acceptable salt thereof, for use in treating inflammatory bowel disease. In an embodiment, the present invention provides a compound of Formula I, or a pharmaceutically acceptable salt thereof, for use in treating lupus nephritis. In an embodiment, the present invention provides a compound of Formula I, or a pharmaceutically acceptable salt thereof, for use in treating systemic lupus erythematosus.

[0045] In an embodiment, the present invention also discloses the use of a compound of Formula I, or a pharmaceutically acceptable salt thereof, for the manufacture of a medicament for treating an inflammatory disease. In an embodiment, the present invention discloses the use of a compound of Formula I, or a pharmaceutically acceptable salt thereof, for the manufacture of a medicament for treating atopic dermatitis. In an embodiment, the present invention discloses the use of a compound of Formula I, or a pharmaceutically acceptable salt thereof, for the manufacture of a medicament for treating rheumatoid arthritis. In an embodiment, the present invention further discloses the use of a compound of Formula I, or a pharmaceutically acceptable salt thereof, for the manufacture of a medicament for treating inflammatory bowel disease. In an embodiment, the present invention further discloses the use of a compound of Formula I, or a pharmaceutically acceptable salt thereof, for the manufacture of a medicament for treating lupus nephritis. In an embodiment, the present invention also discloses the use of a compound of Formula I, or a pharmaceutically acceptable salt thereof, for the manufacture of a medicament for treating systemic lupus erythematosus.

[0046] In an embodiment, the present invention further provides a pharmaceutical composition, comprising a compound of Formula I, or a pharmaceutically acceptable salt thereof, with one or more pharmaceutically acceptable carriers, diluents, or excipients. In an embodiment, the present invention further provides a process for preparing a pharmaceutical composition, comprising admixing a compound of Formula I, or a pharmaceutically acceptable salt thereof, with one or more pharmaceutically acceptable carriers, diluents, or excipients. In an embodiment, the present invention also encompasses novel intermediates and processes for the synthesis of compounds of Formula I.

[0047] As used herein, the terms "treating", "treatment", or "to treat" includes restraining, slowing, stopping, or reversing the progression or severity of an existing symptom or disorder.

[0048] As used herein, the term "patient" refers to a mammal, in particular a human.

[0049] As used herein, the term "effective amount" refers to the amount or dose of compound of the invention, or a pharmaceutically acceptable salt thereof which, upon single or multiple dose administration to the patient, provides the desired effect in the patient under diagnosis or treatment.

[0050] An effective amount can be determined by one skilled in the art by the use of known techniques and by observing results obtained under analogous circumstances. In determining the effective amount for a patient, a number of factors are considered by the attending diagnostician, including, but not limited to: the species of patient; its size, age, and general health; the specific disease or disorder involved; the degree of or involvement or the severity of the disease or disorder; the response of the individual patient; the particular compound administered; the mode of administration; the bioavailability characteristics of the preparation administered; the dose regimen selected; the use of concomitant medication; and other relevant circumstances.

[0051] As used herein, it is understood that Formula I encompasses Formulas Ia, Ib, Ic, Ib(i), Ic(i), Ib(ii), Ic(ii), Ib(iii), Ic(iii), II, IIa, IIb, IIc, III, IIIa, IIIb, and IIIc, and all references to Formula I herein should be read as including Formulas Ia, Ib, Ic, Ib(i), Ic(i), Ib(ii), Ic(ii), Ib(iii), Ic(iii), II, IIa, IIb, IIc, III, IIIa, IIIb, and IIIc.

[0052] As used herein, it is understood that Formula II encompasses Formulas IIa, IIb, and IIc, and all references to Formula II herein should be read as including Formulas IIa, IIb, and IIc.

[0053] As used herein, it is understood that Formula III encompasses Formulas IIIa, IIIb, and IIIc, and all references to Formula III herein should be read as including Formulas IIIa, IIIb, and IIIc.

[0054] As used herein "halogen" refers to F, Cl, Br, and I.

[0055] As used herein "C1-C3 alkyl" refers to CH 3 , CH 2 CH 3 , CH 2 CH 2 CH 3 , and CH(CR 3 ) 2 .

[0056] As used herein "C3-C6 cycloalkyl" refers to cyclopropyl, cyclobutyl, cyclopentyl, and cyclohexyl.

[0057] As used herein "C1-C3 alkoxy" refers to OCH 3 , OCH 2 CH 3 , OCH 2 CH 2 CH 3 , and OCH(CH 3 ) 2 .

[0058] As used herein "C2-C3 alkenyl" refers to HC=CH 2 , and C(CH 3 )=CH 2 .

[0059] As used herein, the ortho and meta positions on phenyl ring A are shown in Formula I below:

[0060] For example, the compound of Formula I' illustrates X connected to phenyl ring A at the meta position: and the compound of Formula I" illustrates X connected to phenyl ring A at the ortho position:

[0061] It is appreciated by one of ordinary skill in the art that when X is connected to phenyl ring A at the ortho position as shown in Formula I", then R 2< is H.

[0062] In addition, as part of the present disclosure but not part of the present invention a compound of the present disclosure can be conjugated with an antibody to form an antibody drug conjugate (ADC) by methods understood by one of skill in the art. One example of such conjugation would include connection of a compound of the present invention to an antibody via a linker compound. Linker compounds known to those of skill in the art include, for example, cleavable linkers and noncleavable linkers. Such an ADC can deliver the compound of the present disclosure to specific target tissues or cells. Accordingly, disclosed herein but not part of the present invention are also ADCs comprising a compound of Formula I. In some embodiments of the present disclosure, the compound of Formula I is conjugated to an antibody via a linker, e.g., a cleavable linker or a noncleavable linker.

[0063] The compounds of the present invention can be formulated as pharmaceutical compositions administered by any route which makes the compound bioavailable including, for example, oral, topical, or subcutaneous administration. Such pharmaceutical compositions can be prepared using techniques and methods known in the art. Such pharmaceutical compositions can be prepared using techniques and methods known in the art (See, e.g., Remington: The Science and Practice of Pharmacy, A. Adejare, Editor, 23nd Edition, published 2020, Elsevier Science; WO 2017 / 062271, and WO 2017 / 210471).

[0064] Furthermore, compounds of the present invention that have the hydroxy group at C21 capped wherein R is: behave as prodrugs and are metabolized in vitro or in vivo to provide the active glucocorticoid receptor agonist wherein R is H.

[0065] Included within the scope of the present invention is a pharmaceutically acceptable salt of Formula I. A pharmaceutically acceptable salt of a compound of the invention, such as a compound of Formula I can be formed, for example, by reaction of an appropriate free base of a compound of the invention with an appropriate pharmaceutically acceptable acid in a suitable solvent such as diethyl ether under standard conditions well known in the art. See, for example, Berge, S.M., et al., "Pharmaceutical Salts," Journal of Pharmaceutical Sciences, 66: 1-19, (1977).

[0066] Certain compounds described in the following preparations may contain a suitable nitrogen protecting group referred to herein as "Pg". It is understood that protecting groups may be varied as appreciated by one of skill in the art depending on the particular reaction conditions and the particular transformations to be performed. The protection and deprotection conditions are well known to the skilled artisan and are described in the literature (See for example "Greene's Protective Groups in Organic Synthesis", Fourth Edition, by Peter G.M. Wuts and Theodora W. Greene, John Wiley and Sons, Inc. 2007). Table 1: Abbreviations and definitions Term Definition ACNacetonitrileaqaqueousÅangstrom(s)BOC / Boctert-butyloxycarbonylC18octadecylsilaneDCMdichloromethaneDEAdiethylamineDIBAL-Hdiisobutylaluminum hydrideDMEAdimethylethylamineDMFN,N-dimethylformamideDMSOdimethyl sulfoxidedppf1,1'-bis(diphenylphosphino)ferroceneequivequivalent(s)ES / MSelectrospray mass spectrometryEtOAcethyl acetateEtOHethanolFAformic acidggram(s)hhour(s)HPLChigh performance liquid chromatographyIPAisopropanolIPAmisopropylamineLliter(s)LCliquid chromatographyLCMSliquid chromatography mass spectrometryLDAlithium diisopropylamideMmolarmbarmillibar(s)MeOHmethanolminminute(s)mLmilliliter(s)mMmillimolarmmolmillimole(s)molmole(s)MSmass spectrometryMTBEmethyl tert-butyl etherMWmolecular weightm / zmass-to-charge rationmnanometer(s)NMRnuclear magnetic resonancePet etherpetroleum etherppmparts per millionROErotating-frame Overhauser enhancementRP-HPLCreverse-phase HPLCrtroom temperaturesatdsaturatedSFCsupercritical fluid chromatographySMstarting materialTHFtetrahydrofuranwtweight

[0067] The compounds of the present invention, or salts thereof, may be readily prepared by a variety of procedures known to one of ordinary skill in the art, some of which are illustrated in the preparations and examples below. One of ordinary skill in the art recognizes that the specific synthetic steps for each of the routes described may be combined in different ways, or in conjunction with steps from different schemes, to prepare compounds of the invention, or salts thereof. The product of each step can be recovered by conventional methods well known in the art, including extraction, evaporation, precipitation, chromatography, filtration, trituration, and crystallization. All substituents unless otherwise indicated, are as previously defined. The reagents and starting materials are readily available to one of ordinary skill in the art. The following preparations, examples, and assays further illustrate the invention.Preparation 1 6-Bromo-2-fluoro-3-methoxybenzaldehyde

[0068]

[0069] Two reactions were carried out in parallel. To a solution of 4-bromo-2-fluoro-1-methoxybenzene (250 g, 1.2 mol) in THF (1500 mL) was added LDA (2 M, 730 mL) slowly at -78 °C, over 30 min. After an additional 30 min, DMF (140 mL, 1.8 mol) was added at -78 °C slowly over 30 min. After 1 h, the two reactions were combined and the mixture was diluted with aq citric acid (2000 mL) and extracted with EtOAc (1500 mL x 2). The combined organic layers were washed with saturated brine (1000 mL) and concentrated under reduced pressure to give a residue. The residue was triturated with petroleum ether (1000 mL) at rt over 12 h to give the title compound (382 g, 67% yield). ES / MS m / z 233.9 (M+H).Preparation 2 2-Fluoro-3-methoxy-6-methylbenzaldehyde

[0070]

[0071] Three reactions were carried out in parallel. 6-Bromo-2-fluoro-3-methoxybenzaldehyde (120 g, 5.3 mol), methylboronic acid (47 g, 7.9 mol), Pd(dppf)Cl 2 (12 g, 0.02 mol), and Cs 2 CO 3 (340 g, 1.1 mol) were added to a mixture of dioxane (600 mL) and water (120 mL). The mixture was stirred at 120 °C. After 12 h, the three reactions were combined and the mixture was diluted with satd aq NH 4 Cl (1000 mL) and extracted with MTBE (1500 mL x 2). The combined organic layers were washed with satd aq NaCl (1000 mL) and concentrated under reduced pressure to give a residue. The residue was purified by normal phase chromatography, eluting with 40:1 Pet ether: EtOAc to give the title compound (180 g, 59% yield). ES / MS m / z 169.3 (M+H).Preparation 3 2-Fluoro-3-hydroxy-6-methylbenzaldehyde

[0072]

[0073] 2-Fluoro-3-methoxy-6-methylbenzaldehyde (175 g, 1.0 mol) was added into DCM (1050 mL). BBr 3 (200 mL, 2.1 mol) was added slowly into the solution at 0 °C. The reaction was stirred at rt. After 1 h, the mixture was diluted with satd aq sodium bicarbonate (1000 mL) until pH=7-8 and was extracted with MTBE (1500 mL x 2). The combined organic layers were washed with satd aq NaCl (1000 mL) and concentrated under reduced pressure to give the title compound (110 g, 68% yield). ES / MS m / z 154.9 (M+H).Preparation 4 tert-Butyl N-[3-[(2-fluoro-3-formyl-4-methyl-phenoxy)methyl]phenyl]carbamate

[0074]

[0075] 2-Fluoro-3-hydroxy-6-methylbenzaldehyde (130 g, 0.84 mol), tert-butyl (3-(bromomethyl)phenyl)carbamate (200 g, 0.70 mol), and potassium carbonate (350 g, 2.5 mol) were added in acetonitrile (780 mL) at rt and then heated to 50 °C. After 5 h, the reaction was diluted with water (600 mL) and extracted with EtOAc (800 mL x 2). The combined organic layers were washed with brine (800 mL) and concentrated under reduced pressure to give a residue. The residue was purified by normal phase chromatography, eluting with 50:1 Pet ether: EtOAc to give crude product. The crude product was triturated with MTBE (500 mL) at rt for 30 min to give the title compound (103 g, 32% yield). ES / MS m / z 382.1 (M+Na).Preparation 5

[0076] (2R,3S,4S,5R,6R)-2-(Acetoxymethyl)-6-(2-((6aR,6bS,7S,8aS,8bS,10S,11aR,12aS,12bS)-10-(3-((3-aminobenzyl)oxy)-2-fluoro-6-methylphenyl)-7-hydroxy-6a,8a-dimethyl-4-oxo-1,2,4,6a,6b,7,8,8a,11a,12,12a,12b-dodecahydro-8bH-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-8b-yl)-2-oxoethoxy)tetrahydro-2H-pyran-3,4,5-triyl triacetate

[0077] 3Å Molecular sieves (5 g) were added to (6aR,6bS,7S,8aS,8bS,10S,11aR,12aS,12bS)-10-(3-((3-aminobenzyl)oxy)-2-fluoro-6-methylphenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-one (150 mg, 0.24 mmol, Example 2 below), 2,3,4,6-tetra-O-acetyl-alpha-D-galactopyranosyl bromide (155 mg, 0.37 mmol), and DCM (5 mL) at rt. After 1 h, the reaction was cooled to 0 °C. Silver(I) oxide (115 mg, 0.49 mmol) and trimethylsilyl trifluoromethanesulfonate (45 µL, 0.24 mmol) were added. After 30 min, the reaction was quenched with satd aq sodium bicarbonate, filtered over diatomaceous earth, and rinsed with DCM (10 mL) and methanol (10 mL). The combined organic layers were concentrated under reduced pressure to give a residue. The residue was purified by reverse phase chromatography, eluting with 1:5 10 mM ammonium bicarbonate water + 5% methanol:acetonitrile to give the title compound (43 mg, 19% yield). ES / MS m / z 948.0 (M+1).Preparation 6 tert-Butyl (2-fluoro-4-methoxyphenoxy)diphenylsilane

[0078]

[0079] To a solution of 2-fluoro-4-methoxyphenol (25 g, 180 mmol) in DMF (350 mL 0.5 M) was added imidazole (18 g, 260 mmol) and tert-butylchlorodiphenylsilane (55 mL, 200 mmol). The reaction was stirred for 18 h at rt. The mixture was diluted with ethyl acetate. The organic solution was washed with water and brine, dried over Na 2 SO 4 , filtered, and concentrated to a crude residue. The residue was purified by normal phase purification, eluting with 5:1 hexanes:ethyl acetate to give the title compound (67 g, 93% yield). 1< H NMR (399.8 MHz, d 6 -DMSO) δ 7.67-7.65 (m, 4H), 7.51-7.44 (m, 6H), 6.82 (dd, J= 2.9, 12.7 Hz, 1H), 6.59 (t, J= 9.4 Hz, 1H), 6.47 (ddd, J= 9.0, 3.0, 1.4 Hz, 1H), 3.64 (s, 3H), 1.06 (s, 9H).Preparation 7 2-Fluoro-3-hydroxy-6-methoxybenzaldehyde

[0080]

[0081] tert-Butyl (2-fluoro-4-methoxyphenoxy)diphenylsilane (56 g, 150 mmol, Preparation 6) was dissolved in 50 mL toluene and concentrated under vacuum for 18 h. The dried solid was dissolved in THF (500 mL) and cooled to -80 °C. n-Butyllithium (1.7 M, 100 mL, 170 mmol) was added rapidly to the cooled solution with a large bore cannula. After 1.5 h, DMF (25 mL, 320 mmol) was added to the solution and the ice bath was removed. After 30 min, 5N aqueous HCl (35 mL) was added to the reaction, then tetrabutylammonium fluoride (1 M in THF, 185 mL, 185 mmol) was added. After 2.5 h, the organic layer was evaporated, acidified with 5N aqueous HCl, and partitioned between ethyl acetate and water (500 mL). The combined organic extracts were washed with water and brine, dried over MgSO 4 , filtered, and concentrated to a crude residue. The residue was purified by normal phase purification, eluting with 1:1 hexanes:ethyl acetate to give the title compound (22 g, 88% yield). MS m / z 170.8 (M+H). Preparation 8 tert-Butyl (3-((2-fluoro-3-formyl-4-methoxyphenoxy)methyl)phenyl)carbamate

[0082]

[0083] 2-Fluoro-3-hydroxy-6-methoxybenzaldehyde (2.5 g, 15 mmol) and tert-butyl N-[3-(bromomethyl)phenyl]carbamate (5.1 g, 18 mmol) were dissolved in acetonitrile (50 mL). Potassium carbonate (2.9 g, 29 mmol) was added to the slurry and the reaction was stirred at rt. After 1 h, the reaction was warmed to 40 °C. After 3 h, the reaction was cooled, filtered, and the solvent was evaporated. The crude residue was purified by normal phase purification, eluting with 7:3 hexanes:EtOAc to give the title compound (3.1 g, 57% yield). MS m / z 374.4 (M-H).

[0084] The following compounds in Table 2 were prepared in a manner essentially analogous to the procedure described in Preparation 8. Table 2: Preparations 9-50Prep. No.StructureES / MS (m / z) (M+H)Starting phenol9 326.02-hydroxybenzal dehyde10 379.02-chloro-6-fluoro-3-hydroxybenzal dehyde11 344.03-fluoro-5-hydroxybenzal dehyde12 360.02-chloro-5-hydroxybenzal dehyde13 360.03-chloro-5-hydroxybenzal dehyde14 344.02-fluoro-5-hydroxybenzal dehyde15 404.02-bromo-5-hydroxybenzal dehyde16 422.0 (M-H)6-bromo-2-fluoro-3-hydroxybenzal dehyde17 356.4 (M-H)3-hydroxy-2-methoxybenzal dehyde18 451.4 (M-H)5-hydroxy-2-iodobenzaldeh yde19 359.26-fluoro-3-hydroxy-2-methylbenzald ehyde20 356.0 (M-H)5-hydroxy-2-methoxybenzal dehyde21 410.6 (M-H)5-hydroxy-2-(trifluorometho xy)benzaldehy de22 374.5 (M-H)6-fluoro-3-hydroxy-2-methoxybenzal dehyde23 363.23-hydroxybenzal dehyde24 360.0 (M-H)2-chloro-6-hydroxybenzal dehyde25 372.0 (M-H)2-fluoro-3-hydroxy-6-methylbenzald ehyde26 378.0 (M-H)6-chloro-2-fluoro-3-hydroxybenzal dehyde27 246.0 (M+H-Boc)2-fluoro-3-hydroxybenzal dehyde28 340.0 (M-H)5-hydroxy-2-methylbenzald ehyde29 344.0 (M-H)2-fluoro-6-hydroxybenzal dehyde30 340.2 (M-H)3-hydroxy-2-methylbenzald ehyde31 374.2 (M-H)2-fluoro-3-hydroxy-4-methoxybenzal dehyde32 360.0 (M-H)4-chloro-3-hydroxybenzal dehyde33 402.2 (M+Na)6-chloro-2-fluoro-3-hydroxybenzal dehyde34 396.2 (M+Na)2-fluoro-3-hydroxy-6-methylbenzald ehyde35 382.2 (M+Na)2-fluoro-3-hydroxy-6-methylbenzald ehyde36 382.2 (M+Na)3-hydroxy-5-methylbenzald ehyde37 379.2 (M+NH 4 )2-chloro-3-hydroxybenzal dehyde38 396.2 (M+Na)2-fluoro-3-hydroxy-6-methylbenzald ehyde39 396.2 (M+Na)2,4-difluoro-3-hydroxybenzal dehyde40 370.4 (M-H)2-ethoxy-5-hydroxybenzal dehyde41 356.4 (M-H)5-hydroxy-2-methoxybenzal dehyde42 374.4 (M-H)2-fluoro-3-hydroxy-6-methoxybenzal dehyde43 344.2 (M-H)2-fluoro-3-hydroxybenzal dehyde44 340.2 (M-H)5-hydroxy-2-methylbenzald ehyde45 362.0 (M+NH 4 )2,6-difluoro-3-hydroxybenzal dehyde46 378.0 (M-H)2-chloro-6-fluoro-3-hydroxybenzal dehyde47 362.2 (M-H)2,6-difluoro-3-hydroxybenzal dehyde48 340.3 (M-H)3-hydroxy-2-methylbenzald ehyde49 372.8 (M+NH 4 )3-hydroxy-2,6-dimethylbenzal dehyde50 406.62-bromo-3-hydroxybenzal dehyde Preparation 51 tert-Butyl (3-((3-formyl-4-(furan-2-yl)phenoxy)methyl)phenyl)carbamate

[0085]

[0086] In a microwave tube, tert-butyl (3-((4-bromo-3-formylphenoxy)methyl)phenyl)carbamate (0.73 g, 1.8 mmol), 2-furylboronic acid (0.30 g, 2.7 mmol), tetrakis(triphenylphosphine)palladium(O) (0.10 g, 0.09 mmol,), and N,N-diisopropylethylamine (1.6 mL, 1.2 mmol) were dissolved in DMF (2 mL, 26 mmol). The tube was flushed with N 2 and capped. The reaction was microwaved at 140 °C for 45 min. The reaction was cooled, poured onto iced water, extracted with EtOAc, and washed with brine. The organic layer was dried over Na 2 SO 4 , filtered, and evaporated to give the title compound (0.70 g, 98% yield). MS m / z 392.2 (M-H).

[0087] The following compounds in Table 3 were prepared in a manner essentially analogous to the procedure described in Preparation 51. Table 3: Preparations 52-55Prep. No.StructureES / MS (m / z) (M+H)Boronic acid52 392.2furan-3-ylboronic acid53 408.4 (M-H)thiophen-2-ylboronic acid54 420.6 (M-H)phenylboronic acid55 402.2 (M-H)phenylboronic acid Preparation 56 tert-Butyl (3'-formyl-[1,1'-biphenyl]-3-yl)carbamate

[0088]

[0089] 3-Bromobenzaldehyde (1.5 g, 8.1 mmol), tert-butyl (3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)carbamate (2.1 g, 6.4 mmol), and potassium carbonate (3.3 g, 24 mmol) were dissolved in 1,4 dioxane (11 mL) and water (3 mL) in a 40-mL reaction vial. The resulting homogenous mixture was stirred and degassed three times. 1,1' Bis(di-tert-butylphosphino)ferrocene dichloropalladium(II) dichloromethane complex (530 mg, 0.81 mmol) was added and the mixture was degassed, capped, and heated to 90 °C for 2.25 h. The reaction was cooled, filtered over diatomaceous earth, and the solvent was evaporated. The crude residue was purified by normal phase chromatography, eluting with 7:3 hexanes:EtOAc to give the title compound (1.5 g, 63% yield). MS m / z 315.4 (M+18).

[0090] The following compound in Table 4 was prepared in a manner essentially analogous to the procedure described in Preparation 56. Table 4: Preparation 57Prep . No.StructureES / MS (m / z) (M+H)Boronic acid57 296.2 (M-H)tert-butyl (4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)carba mate Preparation 58 tert-Butyl (3-(3-formylbenzyl)phenyl)carbamate

[0091]

[0092] 3-(Bromomethyl)benzaldehyde (320 mg, 1.5 mmol), tert-butyl (3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)carbamate (300 mg, 0.94 mmol), and potassium carbonate (410 mg, 3.0 mmol) were dissolved in toluene (9 mL) and water (1 mL) in a vial. The reaction was purged with argon. 1,1' Bis(di-tert-butylphosphino)ferrocene dichloropalladium(II) dichloromethane complex (80 mg, 0.10 mmol) was added, the vial was capped and heated to 100 °C for 1.5 h. The reaction was cooled, filtered over diatomaceous earth, and the solvent was evaporated. The crude residue was purified by normal phase chromatography, eluting with 7:3 heptane:EtOAc to give the title compound (300 mg, 54% yield). MS m / z 329.4 (M+18).

[0093] The following compounds in Table 5 were prepared in a manner essentially analogous to the procedure described in Preparation 58. Table 5: Preparations 59-60Prep. No.StructureES / MS (m / z) (M+H)Boronic acid / ester59 329.4 (M+NH 4 )tert-butyl (2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)car bamate60 329.4 (M+NH 4 )tert-butyl (4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)car bamate Preparation 61 2,6-Difluoro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzaldehyde

[0094]

[0095] tert-Butyl 3-(bromomethyl)phenylcarbamate (1.5 g, 5.0 mmol), 2,6-difluoro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzaldehyde (1.5 g, 5.6 mmol), and potassium carbonate (2.1 g, 3.0 mmol) were placed in a reaction vial with water (1 mL) and toluene (9 mL). The reaction mixture was bubbled with N 2 , 1,1'-bis(di-tert-butylphosphino)ferrocene dichloropalladium(II) dichloromethane complex (310 mg, 0.37 mmol) was added, and the vial was capped and heated at 100 °C for 10 min. The reaction was cooled, filtered, and the filtrate was evaporated. The crude residue was purified by normal phase chromatography, eluting with 1:1 heptane:EtOAc to give the title compound (1.38 g, 3.85 mmol, 77% yield). MS m / z 365.2 (M+NH 4 ).

[0096] The following compounds in Table 6 were prepared in a manner essentially analogous to the procedure described in Preparation 61. Table 6: Preparations 62-66Prep. No.StructureES / MS (m / z) (M+H)Boronic acid / ester62 No ion2-fluoro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzaldehy de63 381.0 (M+NH 4 )(4-chloro-2-fluoro-3-formylphenyl )boronic acid64 381.2 (M+NH 4 )(4-chloro-2-fluoro-3-formylphenyl )boronic acid65 363.2 (M+NH 4 )(4-chloro-3-formylphenyl )boronic acid66 363.2 (M+H)(4-chloro-3-formylphenyl )boronic acid Preparation 67 tert-Butyl (4-(3-formylphenoxy)phenyl)carbamate

[0097]

[0098] (3-Formylphenyl)boronic acid (610 mg, 4.1 mmol), tert-butyl (4-hydroxyphenyl)carbamate (420 mg, 2.0 mmol), copper(II) acetate (370 mg, 2.0 mmol), triethylamine (1.4 mL, 10 mmol), and 4 Å molecular sieves (500 mg) were added in DCM (15 mL) in a vial. The reaction was incubated at rt for 10 h. The reaction was filtered over diatomaceous earth and the solvent was evaporated. The crude residue was purified by normal phase chromatography, eluting with 7:3 hexanes:EtOAc to give the title compound (180 mg, 29% yield). MS m / z 312.2 (M-H).

[0099] The following compounds in Table 7 were prepared in a manner essentially analogous to the procedure described in Preparation 67. Table 7: Preparation 68Prep. No.StructureES / MS (m / z) (M+H)Phenol68 312.2 (M-H)tert-butyl (3-hydroxyphen yl)carbamate Preparation 69 tert-Butyl (4-(3-formylphenoxy)phenyl)carbamate

[0100]

[0101] 5-Hydroxy-2-methoxybenzaldehyde (1.00 g, 6.57 mmol), [4-(tert-butoxycarbonylamino)phenyl]boronic acid (3.12 g, 13.2 mmol), copper(II) acetate (1.19 g, 6.57 mmol), and 4 Å molecular sieves (1.0 g) were added to a flask. DCM (60 mL) and triethylamine (4.6 mL, 33 mmol) were then added. The reaction mixture was stirred at rt overnight. More [4-(tert-butoxycarbonylamino)phenyl]boronic acid (1.1 g, 4.6 mmol) and copper(II) acetate (400 mg, 2.2 mmol) were added and the reaction mixture was stirred at rt for three days. The reaction was filtered and the solvent was evaporated. The crude residue was purified by normal phase chromatography, eluting with heptane:EtOAc to give the title compound (400 mg, 18% yield). MS m / z 361.0 (M+NH 4 ).

[0102] The following compounds in Table 8 were prepared in a manner essentially analogous to the procedure described in Preparation 69. Table 8: Preparation 70Prep. No.StructureES / MS (m / z) (M+H)Boronic acid70 361.0 (M+NH 4 )[3-(tert-butoxycarbon ylamino)phen yl]boronic acid Preparation 71 tert-Butyl (3-((2-fluoro-3-formylphenyl)ethynyl)phenyl)carbamate

[0103]

[0104] 3-Ethynyl-2-fluorobenzaldehyde (0.25 g, 1.7 mmol) was mixed with tert-butyl N-(3-iodophenyl)carbamate (0.55 g, 1.7 mmol), bis(triphenylphosphine)palladium(II) dichloride (0.025 g, 0.036 mmol), and copper(I) iodide (0.01 g., 0.05 mmol) in triethylamine (10 mL, 72 mmol) under N 2 . The reaction mixture was stirred at rt overnight. The reaction mixture was diluted with EtOAc and filtered through diatomaceous earth. The filtrate was washed with 1 M aq HCl, brine, dried over Na 2 SO 4 , and filtered. The solvent was evaporated to give the title compound (0.57 g, 100% yield). MS m / z 338.2 (M-H).

[0105] Wherein G 1< is

[0106] Wherein L is Preparation 72 2-(6-Fluoro-3-methoxy-2-methylphenyl)-1,3-dioxolane

[0107]

[0108] To a microwave vial, added 2-(2-bromo-6-fluoro-3-methoxyphenyl)-1,3-dioxolane (970 mg, 3.5 mmol), trimethylboroxine (50 mass%) in THF (600 µL, 4.3 mmol), and cesium carbonate (2.3 g, 7.1 mmol) in 1,4-dioxane (12 mL, 140 mmol) and water (2 mL, 110 mmol). Degassed the solution with N 2 for 2 min. [1,1'-Bis(diphenylphosphino)ferrocene]dichloro palladium(II) (130 mg, 0.17 mmol) was added and degassed the solution with N 2 for 2 min. The vial was capped and microwaved at 110 °C for 1 h. The reaction mixture was diluted with water (10 mL) and extracted with EtOAc (10 mL). The organic layer was dried with Na 2 SO 4 , filtered through paper, and rotary evaporated to a crude oil. The crude oil was purified by normal phase chromatography, eluting with 7:3 hexanes:MTBE to give the title compound (0.61 g, 82% yield). MS m / z 212.8 (M+H).

[0109] The following compounds in Table 9 were prepared in a manner essentially analogous to the procedure described in Preparation 72. Table 9: Preparations 73-78Prep. No.StructureES / MS (m / z) (M+H)Bromide73 No ion*tert-butyl (3-((4-bromo-2-fluoro-3-formylbenzyl)thi o)phenyl)carbam ate74 305.9 (M-Boc+H)methyl 6-bromo-3-(((2-((tert-butoxycarbonyl) amino)phenyl)th io)methyl)-2-fluorobenzoate75 359.0tert-butyl (3-((4-bromo-2-fluoro-3-formylbenzyl)a mino)phenyl)car bamate76 No ion**tert-butyl (2-((4-bromo-2-fluoro-3-formylbenzyl)ox y)phenyl)carbam ate77 315.9methyl (E)-6-bromo-2-fluoro-3-(4-nitrostyryl)benzo ate78 359.0tert-butyl (2-((4-bromo-2-fluoro-3-formylbenzyl)a mino)phenyl)car bamate* 1< H NMR (400.14 MHz, DMSO): δ 10.40 (s, 1H), 9.39 (s, 1H), 7.55-7.50 (m, 2H), 7.26 (d, J= 8.3 Hz, 1H), 7.19 (t, J= 7.9 Hz, 1H), 7.08 (d, J= 7.9 Hz, 1H), 6.96 (d, J= 7.8 Hz, 1H), 4.22 (s, 2H), 1.46 (s, 10H) ** 1< H NMR (400.21 MHz, DMSO): δ 10.45 (s, 1H), 7.97 (s, 1H), 7.78 (t, J= 7.8 Hz, 1H), 7.65-7.61 (m, 1H), 7.22-7.20 (m, 1H), 7.14-7.12 (m, 1H), 7.07-7.02 (m, 1H), 6.95-6.91 (m, 1H), 5.21 (s, 2H), 2.57 (s, 3H), 1.43 (s, 9H) Preparation 79 6-Fluoro-3-hydroxy-2-methylbenzaldehyde

[0110]

[0111] Boron tribromide in DCM (14 mL, 14 mmol, 1 mol / L) was added over a period of 2 min to a solution of 2-(6-fluoro-3-methoxy-2-methylphenyl)-1,3-dioxolane (600 mg, 2.8 mmol) in DCM (14 mL, 220 mmol) cooled to 0 °C. The bath was removed after the addition. After 30 min, the reaction was quenched with satd aq NH 4 Cl. The reaction was diluted with DCM, washed with 2 M aq NaOH, and then washed with 5 M aq HCl. The organic layer was dried with Na 2 SO 4 , filtered through paper, and rotary evaporated to a crude residue. The crude residue was purified by normal phase chromatography, eluting with 7:3 hexanes:EtOAc to give the title compound (130 mg, 30% yield). MS m / z 153.0 (M-H).Preparation 80 tert-Butyl (4-fluoro-2-methoxyphenoxy)diphenylsilane

[0112]

[0113] To a solution of 4-fluoro-2-methoxy-phenol (2.3 g, 16 mmol) in DCM (35 mL) was added imidazole (2.8 g, 41 mmol) and tert-butylchlorodiphenylsilane (6 mL, 23 mmol). After 1.75 h, the solvent was evaporated, and the residue was partitioned between 200 mL of 10% EtOAc in hexanes and 100 mL water. The organics were washed once with brine, dried over MgSO 4 , filtered, and evaporated. The crude residue was purified by normal phase chromatography, eluting with 9:1 hexanes:EtOAc to give the title compound (6.7 g, quantitative yield). 1< H NMR (399.8 MHz, d 6 -DMSO) δ7.64 (dd, J= 1.5, 7.9 Hz, 4H), 7.48-7.43 (m, 6H), 6.82 (dd, J= 2.9, 10.5 Hz, 1H), 6.60 (dd, J= 5.9, 8.8 Hz, 1H), 6.48 (td, J= 8.5, 3.0 Hz, 1H), 3.56 (s, 3H), 1.05 (s, 9H)Preparation 81 6-Fluoro-3-hydroxy-2-methoxybenzaldehyde

[0114]

[0115] tert-Butyl (4-fluoro-2-methoxyphenoxy)diphenylsilane (3.2 g, 8.5 mmol) was dissolved in tetrahydrofuran (30 mL) and cooled to -78 °C. n-Butyllithium (7 mL, 11 mmol, 1.6 M) was added over 3 minutes. After 1.5 h, DMF (2 mL) was added at -78 °C. After 1 h, added about 4 mL of 10% aq NH 4 Cl and warmed to rt over 1.5 h. Evaporated the solvent to a crude residue, then made acidic with 1 M aq HCl, and partitioned between water and 300 mL EtOAc. The organic layer was washed with water, brine, dried over MgSO 4 , filtered, and evaporated. The crude residue was purified by normal phase chromatography, eluting with 3:2 hexanes:EtOAc to give the title compound (0.79 g, 55% yield). MS m / z 171.0 (M+H).Preparation 82 tert-Butyl (3-((4-cyclopropyl-3-(1,3-dioxolan-2-yl)-2-fluorophenoxy)methyl)phenyl)carbamate

[0116]

[0117] tert-Butyl (3-((4-bromo-3-(1,3-dioxolan-2-yl)-2-fluorophenoxy)methyl)phenyl)carbamate (200 mg, 0.43 mmol), cyclopropyl boronic acid (0.21 g, 2.4 mmol), and potassium phosphate tribasic (0.28 g, 1.3 mmol) were placed in a 25 mL vial purged with N 2 . Toluene (3 mL) and water (0.75 mL) were added. The reaction mixture was degassed with N 2 for 5 min and then tetrakis(triphenylphosphine)palladium(0) (0.10 g, 0.09 mmol) was added in one portion. The reaction was heated to 100 °C overnight. Upon cooling to rt, EtOAc and water were added; the phases were separated, and the aqueous layer was extracted twice with EtOAc. The combined organic layers were dried over Na 2 SO 4 , filtered, and concentrated to a crude residue. The crude residue was purified by normal phase chromatography, eluting with 1:1 hexanes:EtOAc to give the title compound (170 mg, 94% yield). MS m / z 428.4 (M-H).Preparation 83 (2,6-Dimethyl-3-nitrophenyl)methylene diacetate

[0118]

[0119] 2,6-Dimethyl-3-nitrobenzaldehyde (1.9 g, 10 mmol) was dissolved in DCM (23 mL), then acetic anhydride (1.3 mL, 14 mmol) and copper(II) trifluoromethanesulfonate (41 mg, 0.11 mmol) were added. The solution was stirred at rt for 3.5 h. The reaction was quenched with satd aq NaHCO 3 . The organic layer was separated, washed with water, brine, dried over Na 2 SO 4 , filtered, and concentrated to a crude residue. The crude residue was purified by normal phase chromatography, eluting with 3:2 hexanes:EtOAc to give the title compound (2.4 g, 81% yield). 1< H NMR (400.13 MHz, DMSO-d6): 7.96 (s, 1H), 7.80 (d, J= 8.3 Hz, 1H), 7.35 (d, J= 8.4 Hz, 1H), 2.58 (s, 3H), 2.53 (s, 2H), 2.12 (s, 6H).Preparation 84 (3-Amino-2,6-dimethylphenyl)methylene diacetate

[0120]

[0121] Sulfided 5wt% platinum on carbon (1.0 g, 5.2 mmol) was added to a 500-mL Parr shaker bottle and degassed with N 2 . Added 25 mL EtOAc, then added (2,6-dimethyl-3-nitrophenyl)methylene diacetate (2.7 g, 9.6 mmol) in 25 mL EtOAc to the bottle. The bottle was sealed, purged with N 2 , purged with H 2 , and pressurized to 413,685 Pa (60 psi) H 2 for 1.5 h at rt. The reaction mixture was filtered and concentrated to give the title compound (2.1 g, quant yield). MS m / z 251.8 (M+H).Preparation 85 (3-((3-((tert-Butoxycarbonyl)amino)benzyl)amino)-2,6-dimethylphenyl)methylene diacetate

[0122]

[0123] A mixture of (3-amino-2,6-dimethylphenyl)methylene diacetate (276 mg, 1.10 mmol) and potassium carbonate (435 mg, 3.15 mmol) in DMF (3 mL) was stirred at rt for 1 h. tert-Butyl N-[3-(bromomethyl)phenyl]carbamate (300 mg, 1.05 mmol) was added to the slurry and the reaction was stirred at 50 °C for 1 h. After cooling, the reaction mixture was partitioned between ethyl acetate and water. The phases were separated. The organic phase was transferred to a round-bottom flask, and the solvent evaporated in vacuo. Residual DMF was evaporated (azeotroped) with xylenes giving residue as a clear paste. The crude residue was purified by normal phase purification, eluting with 1:1 EtOAc:hexanes to give the title compound (363 mg, 76% yield). MS m / z 457.2 (M+H). Preparation 86 Methyl 3-((3-((tert-butoxycarbonyl)amino)benzyl)amino)-2-fluoro-6-methylbenzoate

[0124]

[0125] tert-Butyl (3-formylphenyl)carbamate (1.2 g, 5.2 mmol), methyl 3-amino-2-fluoro-6-methylbenzoate (950 mg, 4.8 mmol), and acetic acid (0.55 mL, 9.6 mmol) was dissolved in methanol (5 mL) and cooled to 0 °C. Sodium cyanoborohydride (0.61 g, 9.5 mmol) was carefully added into the solution. The ice bath was removed, and the reaction mixture stirred at rt overnight under N 2 . The reaction was quenched by addition of water (10 mL). The reaction mixture was partitioned between EtOAc and water. The combined organic extracts were washed with brine, dried with Na 2 SO 4 , filtered, and concentrated to a crude residue. The crude residue was purified by normal phase chromatography, eluting with 3:2 Pet ether:EtOAc to give the title compound (1.9 g, 75% yield). MS m / z 389.0 (M+H).

[0126] The following compound in Table 10 was prepared in a manner essentially analogous to the procedure described in Preparation 86. Table 10: Preparation 87Prep. No.StructureES / MS (m / z) (M+H)Formyl starting material87 389.0tert-butyl (2-formylphenyl)c arbamate Preparation 88 Methyl 6-bromo-2-fluoro-3-formylbenzoate

[0127]

[0128] N-Bromosuccinimide (5.8 g, 31 mmol) was added to a solution of methyl 6-bromo-2-fluoro-3-methylbenzoate (3.9 g, 14 mmol) in carbon tetrachloride (36 mL), followed by 2,2'-azobis(2-methylpropionitrile (0.24 g, 1.4 mmol), and the reaction mixture was stirred at 85 °C overnight. The mixture was diluted with DCM, washed with brine, dried over Na 2 SO 4 , and concentrated to a crude residue. The residue was dissolved in ACN and purified by preparative C18 HPLC (35%-60% water [0.225% FA]-ACN). The eluent was concentrated to give methyl 6-bromo-3-(dibromomethyl)-2-fluorobenzoate (1.9 g, 4.6 mmol). The material was dissolved in ethanol (15 mL). A mixture of silver nitrate (2.0 g, 12 mmol) in water (10 mL) was added and the reaction mixture was heated at 75 °C for 6 h under N 2 . The reaction mass was filtered and washed with EtOAc. The filtrate was concentrated to giver a crude residue. The crude residue was purified by normal phase chromatography, eluting with 8% EtOAc:Pet ether to give the title compound (1.1 g, 91% yield). Preparation 89 Methyl 6-bromo-3-(((3-((tert-Butoxycarbonyl)amino)phenyl)amino)methyl)-2-fluorobenzoate

[0129]

[0130] Methyl 6-bromo-2-fluoro-3-formylbenzoate (1.0 g, 3.7 mmol), tert-butyl N-(3-aminophenyl)carbamate (870 mg, 4.1 mmol), and acetic acid (0.43 mL, 7.5 mmol) were dissolved in methanol (9 mL) and cooled to 0 °C. Sodium cyanoborohydride (480 mg, 7.5 mmol) was carefully added into the solution. The ice bath was removed, and the reaction mixture stirred at rt overnight under N 2 . The reaction was quenched by addition of water (30 mL). The reaction mixture was partitioned between EtOAc and water. The combined organic extracts were washed with brine, dried with Na 2 SO 4 , filtered, and concentrated to a crude residue. The crude residue was purified by normal phase chromatography, eluting with 7:3 Pet ether:EtOAc to give the title compound (1.7 g, 89% yield). MS m / z 454.9 (M+H).

[0131] The following compound in Table 11 was prepared in a manner essentially analogous to the procedure described in Preparation 89. Table 11: Preparation 90Prep. No.StructureES / MS (m / z) (M+H)Formyl starting material90 454.9methyl 6-bromo-2-fluoro-3-formylbenzoate Preparation 91 Methyl 3-((3-((tert-butoxycarbonyl)amino)benzyl)(methyl)amino)-2-fluoro-6-methylbenzoate

[0132]

[0133] To a solution of methyl 3-((3-((tert-butoxycarbonyl)amino)benzyl)amino)-2-fluoro-6-methylbenzoate (1.7 g, 3.3 mmol) in methanol (5 mL) was added sodium cyanoborohydride (420 mg, 6.5 mmol) and acetic acid (0.5 mL, 9 mmol). Formaldehyde in water (730 µL, 9.8 mmol, 37 mass%) was then added at 25 °C. The mixture was stirred at rt overnight under N 2 . The crude mixture was purified by normal phase chromatography, eluting with 4:1 Pet ether:EtOAc to give the title compound (1.3 g, 92% yield). MS m / z 403.0 (M+H). Preparation 92 tert-Butyl (3-(((2-fluoro-3-(hydroxymethyl)-4-methylphenyl)(methyl)amino)methyl)phenyl)carbamate

[0134]

[0135] To a solution methyl 3-((3-((tert-butoxycarbonyl)amino)benzyl)(methyl)amino)-2-fluoro-6-methylbenzoate (1.2 g, 2.8 mmol) in DCM (10 mL) was added DIBAL-H in toluene (7 mL, 7.0 mmol, 1.0 mol / L) at 0 °C. The reaction mixture was warmed to rt for 3 h. The solution was cooled back to 0 °C and satd aq Rochelle salt and DCM were added, followed by extraction with DCM. The organic layer was washed with brine, dried over Na 2 SO 4 , passed through a silica gel plug, and concentrated to a crude residue. The residue was purified by normal phase chromatography, eluting with 1:1 Pet ether:EtOAc to give the title compound (640 mg, 57% yield). MS m / z 375.0 (M+H). The following compounds in Table 12 were prepared in a manner essentially analogous to the procedure described in Preparation 92. Table 12: Preparations 93-98Prep. No.StructureES / MS (m / z) (M+H)Ester SM93 278.0 (M-Boc+H)methyl 3-(((2-((tert-butoxycarbonyl)a mino)phenyl)thio )methyl)-2-fluoro-6-methylbenzoate94 426.9methyl 6-bromo-3-(((3-((tert-butoxycarbonyl)a mino)phenyl)ami no)methyl)-2-fluorobenzoate95 361.0methyl 3-((2-((tert-butoxycarbonyl)a mino)benzyl)ami no)-2-fluoro-6-methylbenzoate96 361.2methyl 3-((3-((tert-butoxycarbonyl)a mino)benzyl)ami no)-2-fluoro-6-methylbenzoate97 No ion*methyl 3-(4-((tert-butoxycarbonyl)a mino)phenethyl)-2-fluoro-6-methylbenzoate98 426.9methyl 6-bromo-3-(((2-((tert-butoxycarbonyl)a mino)phenyl)ami no)methyl)-2-fluorobenzoate* 1< H NMR (400.14 MHz, DMSO): δ 9.23 (s, 1H), 7.35-7.31 (m, 2H), 7.09-7.02 (m, 3H), 6.89 (d, J= 7.8 Hz, 1H), 4.92 (t, J= 5.3 Hz, 1H), 4.49-4.48 (m, 2H), 4.03 (q, J= 7.1 Hz, 1H), 2.79-2.72 (m, 4H), 2.33 (s, 3H), 1.46 (s, 9H). Preparation 99 tert-Butyl (3-(((2-fluoro-3-formyl-4-methylphenyl)(methyl)amino)methyl)phenyl)carbamate

[0136]

[0137] To a solution of tert-butyl (3-(((2-fluoro-3-(hydroxymethyl)-4-methylphenyl)(methyl)amino)methyl)phenyl)carbamate (590 mg, 1.5 mmol) in EtOAc (5 mL) was added 2-iodoxybenzoic acid (630 mg, 2.2 mmol). The reaction mixture was stirred at 80 °C for 6 h. The solids were filtered out and the filtrate was concentrated to a crude residue. The residue was purified by normal phase chromatography, eluting with 7:3 Pet ether:EtOAc to give the title compound (580 mg, 94% yield). MS m / z 373.0 (M+H).

[0138] The following compounds in Table 13 were prepared in a manner essentially analogous to the procedure described in Preparation 99. Table 13: Preparations 100-104Prep. No.StructureES / MS (m / z) (M+H)Alcohol starting material100 No ion*(6-bromo-3-(bromomethyl)-2-fluorophenyl)met hanol101 275.9 (M-Boc+H)tert-butyl (2-((2-fluoro-3-(hydroxymethyl)-4-methylbenzyl)thi o)phenyl)carbam ate102 424.9tert-butyl (3-((4-bromo-2-fluoro-3-(hydroxymethyl) benzyl)amino)ph enyl)carbamate103 No ion**tert-butyl (4-(2-fluoro-3-(hydroxymethyl)-4-methylphenethyl) phenyl)carbamate104 425.0tert-butyl (2-((4-bromo-2-fluoro-3-(hydroxymethyl) benzyl)amino)ph enyl)carbamate* 1< H NMR (400.15 MHz, DMSO): δ 10.31 (d, J= 0.8 Hz, 1H), 7.90-7.86 (m, 1H), 7.78 (dd, J= 0.8, 8.4 Hz, 1H), 4.84 (d, J= 1.0 Hz, 2H) ** 1< H NMR (400.15 MHz, DMSO): δ 10.42 (s, 1H), 9.23 (s, 1H), 7.44-7.40 (m, 1H), 7.36-7.33 (m, 2H), 7.09-7.05 (m, 3H), 2.92-2.81 (m, 4H), 2.50 (s, 3H), 1.47 (s, 9H). Preparation 105 tert-Butyl (4-(2-(2-fluoro-3-formyl-4-methylphenoxy)ethyl)phenyl)carbamate

[0139]

[0140] To a solution of 2-fluoro-3-hydroxy-6-methylbenzaldehyde (250 mg, 1.5 mmol) and 4-((tert-butoxycarbonyl)amino)phenethyl 4-methylbenzenesulfonate (760 mg, 1.9 mmol) in acetonitrile (10 mL) was added potassium carbonate (670 mg, 4.9 mmol). The suspension was stirred at 80 °C for 16 h. The reaction mixture was concentrated under reduced pressure to give a residue. The residue was diluted with water (40 mL), extracted with EtOAc (20 mL). The combined organic layers were washed with brine (20 mL), dried over anhydrous Na 2 SO 4 , filtered, and concentrated under reduced pressure to give a residue. The residue was purified by normal phase chromatography, eluting with 17:3 Pet ether:EtOAc to give the title compound (510 mg, 85% yield). 1< H NMR (400.15 MHz, CDCl 3 ): δ 10.47 (s, 1H), 7.24 (d, J= 8.4 Hz, 2H), 7.15 (d, J= 8.5 Hz, 2H), 6.96 (t, J= 8.4 Hz, 1H), 6.82 (d, J= 8.4 Hz, 1H), 6.37-6.35 (m, 1H), 4.12 (t, J= 7.0 Hz, 2H), 3.01 (t, J= 6.9 Hz, 2H), 2.45 (s, 3H), 1.45 (s, 8H).Preparation 106 (6-Bromo-3-(bromomethyl)-2-fluorophenyl)methanol

[0141]

[0142] To a solution of 6-bromo-3-(bromomethyl)-2-fluorobenzoic acid (4.9 g, 11 mmol) in THF (100 mL) under a nitrogen atmosphere and cooled in an ice bath, borane-THF complex in THF (35 mL, 35 mmol, 1 mol / L) was added dropwise. The reaction mixture was allowed to warm to rt for overnight. The reaction was quenched by addition of MeOH (100 mL) and concentrated in vacuo. The resulting residue was partitioned between EtOAc (100 mL) and 1 M HCl (30 mL) and the aqueous layer was extracted once with EtOAc (100 mL). The combined organic extracts were dried with Na 2 SO 4 , filtered, and concentrated to give a crude residue. The residue was purified by normal phase chromatography, eluting with 7:3 Pet ether:EtOAc to give the title compound (2.9 g, 62% yield). 1< H NMR (400.15 MHz, DMSO): δ7.50-7.42 (m, 2H), 5.38-5.23 (m, 1H), 4.70 (d, J= 0.5 Hz, 2H), 4.59 (d, J= 1.5 Hz, 2H).

[0143] Wherein G 2< is

[0144] Wherein J is hydrogen or Boc.Preparation 107 tert-Butyl (3-((4-bromo-2-fluoro-3-formylbenzyl)thio)phenyl)carbamate

[0145]

[0146] To a mixture of 6-bromo-3-(bromomethyl)-2-fluorobenzaldehyde (620 mg, 1.9 mmol) and tert-butyl N-(3-sulfanylphenyl)carbamate (500 mg, 2.0 mmol) in DCM (10 mL) was added triethylamine (530 µL, 3.8 mmol) under N 2 . The mixture was stirred at rt for 2 h. The reaction mixture was partitioned between DCM (30 mL) and water (30 mL). The combined organic extracts were concentrated under vacuum to give the crude residue. The residue was purified by normal phase chromatography, eluting with 3:1 Pet ether:EtOAc to give the title compound (780 mg, 89% yield). 1< H NMR (400.15 MHz, DMSO): δ 10.19 (s, 1H), 9.39 (s, 1H), 7.57-7.51 (m, 2H), 7.47 (s, 1H), 7.27 (d, J= 8.6 Hz, 1H), 7.19 (t, J= 7.9 Hz, 1H), 6.96 (d, J= 7.8 Hz, 1H), 4.21 (s, 2H), 1.46 (s, 9H).

[0147] The following compound in Table 14 was prepared in a manner essentially analogous to the procedure described in Preparation 107. Table 14: Preparation 108Prep. No.StructureES / MS (m / z) (M+H)Thiol starting material108 371.82-aminobenzen ethiol Preparation 109 Methyl 6-bromo-3-(((2-((tert-butoxycarbonyl)amino)phenyl)thio)methyl)-2-fluorobenzoate

[0148]

[0149] To a solution of methyl 3-(((2-aminophenyl)thio)methyl)-6-bromo-2-fluorobenzoate (1.3 g, 3.4 mmol) in tert-butanol (13 mL, 140 mmol) was added di-tert-butyl dicarbonate (3.5 mL, 15 mmol). The mixture was stirred at 50 °C overnight under N 2 . The reaction was concentrated under vacuum to give the crude residue. The residue was purified by normal phase chromatography, eluting with 10:1 Pet ether:EtOAc to give the title compound (1.6 g, quantitative yield). MS m / z 371.8 (M-Boc+H).Preparation 110 (3-Bromo-2-fluoro-4-methylphenyl)methanol

[0150]

[0151] To a solution of 3-bromo-2-fluoro-4-methylbenzaldehyde (2 g, 6.6 mmol) in MeOH was added sodium borohydride (620 mg, 16 mmol) at 0 °C. The mixture was stirred for 1 h. The mixture was slowly quenched with 1 M aq HCl (30 mL) under N 2 , adjusting to pH 6. The reaction mixture was concentrated under vacuum to give crude residue. The residue was purified by normal phase chromatography, eluting with 1:2 Pet ether:EtOAc to give the title compound (820 mg, 51% yield).Preparation 111 tert-Butyl (3-((3-bromo-2-fluoro-4-methylbenzyl)oxy)phenyl)carbamate

[0152]

[0153] To a solution of (3-bromo-2-fluoro-4-methylphenyl)methanol (650 mg, 2.7 mmol), tert-butyl (3-hydroxyphenyl)carbamate (870 mg, 4.0 mmol), and tetrabutylphosphine (1.1 g, 5.4 mmol) in THF (10 mL, 120 mmol) was added N,N,N',N'-tetramethylazodicarboxamide (940 mg, 5.4 mmol). The reaction mixture was stirred at rt for 2 h under anhydrous N 2 . The reaction mixture was partitioned between EtOAc (100 mL) and water (100 mL). The combined organic extracts were washed with brine (200 mL), dried with Na 2 SO 4 , filtered, and concentrated under vacuum to give crude residue. The residue was purified by normal phase chromatography, eluting with 9:1 Pet ether:EtOAc to give the title compound (1.2 g, 96% yield). MS m / z 355.8 (M-tBu+H).Preparation 112 tert-Butyl (3-((2-fluoro-3-formyl-4-methylbenzyl)oxy)phenyl)carbamate

[0154]

[0155] To a solution of tert-butyl (3-((3-bromo-2-fluoro-4-methylbenzyl)oxy)phenyl)carbamate (0.82 g, 1.8 mmol) in THF (5 mL, 62 mmol) was added isopropylmagnesium chloride lithium chloride complex solution in THF (3.1 mL, 4.0 mmol, 1.3 mol / L) at 0 °C and stirred for 30 min. DMF (450 µL, 5.7 mmol) was added to the mixture at 0 °C. The mixture was warmed to rt for 1.5 h and then quenched by addition of satd aq NH 4 Cl (5 mL). The reaction mixture was partitioned between EtOAc (30 mL) and water (30 mL). The combined organic extracts were concentrated under vacuum to give the crude product. The residue was purified by normal phase chromatography, eluting with 95:5 Pet ether:EtOAc to give the title compound (220 mg, 25% yield). MS m / z 259.9 (M-Boc+H).Preparation 113 tert-Butyl (2-((4-bromo-2-fluoro-3-formylbenzyl)oxy)phenyl)carbamate

[0156]

[0157] Cesium carbonate (230 mg, 0.71 mmol) was added to a solution of tert-butyl (2-hydroxyphenyl)carbamate (100 mg, 0.47 mmol) and 6-bromo-3-(bromomethyl)-2-fluorobenzaldehyde (160 mg, 0.51 mmol) in DMF (3 mL). The reaction mixture was stirred at rt for 1 h under N 2 and then quenched with the addition of water. The reaction mixture was partitioned between EtOAc (20 mL) and water (20 mL). The combined organic extracts were concentrated under vacuum to give the crude product. The residue was purified by normal phase chromatography, eluting with 4:1 Pet ether:EtOAc to give the title compound (210 mg, quantitative yield). 1< H NMR (400.21 MHz, DMSO): δ 10.24 (s, 1H), 8.08 (s, 1H), 7.82 (t, J= 7.9 Hz, 1H), 7.69 (d, J= 8.3 Hz, 1H), 7.63 (d, J= 7.6 Hz, 1H), 7.10 (dd, J= 1.0, 8.1 Hz, 1H), 7.06-7.02 (m, 1H), 6.95-6.91 (m, 1H), 5.21 (s, 2H), 1.44 (s, 9H). Preparation 114 tert-Butyl (2-(((2-fluoro-3-formyl-4-methylphenyl)thio)methyl)phenyl)carbamate

[0158]

[0159] To a solution of S-(2-((tert-butoxycarbonyl)amino)benzyl) ethanethioate (670 mg, 2.2 mmol) in 1,4-dioxane (10 mL) and water (2 mL) was added 3-bromo-2-fluoro-6-methyl-benzaldehyde (550 mg, 1.8 mmol), 2-dicyclohexylphosphino-2',4',6'-triisopropylbiphenyl (220 mg, 0.44 mmol), potassium carbonate (610 mg, 4.4 mmol), and tris(dibenzylideneacetone)dipalladium(0) (210 mg, 0.22 mmol). The mixture was heated to 100 °C overnight. Upon completion, the reaction mixture was concentrated under reduced pressure. The residue was diluted with water (20 mL) and extracted with EtOAc (20 mL x 2). The combined organic layers were washed with brine (40 mL), dried over Na 2 SO 4 , and concentrated in vacuo to give a residue. The residue was purified by normal phase chromatography, eluting with 95:5 Pet ether:EtOAc to give the title compound (670 mg, 54% yield). MS m / z 275.9 (M-Boc+H).

[0160] The following compounds in Table 15 were prepared in a manner essentially analogous to the procedure described in Preparation 114. Table 15: Preparations 115-116Prep. No.StructureES / MS (m / z) (M+H)Thioate SM115 398.2 (M+Na)S-(3-((tert-butoxycarbonyl)a mino)benzyl) ethanethioate116 275.9 (M-Boc+H)S-(3-((tert-butoxycarbonyl)a mino)benzyl) ethanethioate Preparation 117 tert-Butyl (2-(((2-fluoro-3-formyl-4-methylphenyl)amino)methyl)phenyl)carbamate

[0161]

[0162] To a solution tert-butyl (2-(((2-fluoro-3-(hydroxymethyl)-4-methylphenyl)amino)methyl)phenyl)carbamate (950 mg, 2.4 mmol) in THF (20 mL) was added manganese dioxide (2.2 g, 25 mmol) at rt. The resulting mixture was stirred at 70 °C overnight. Additional manganese dioxide (2.2 g, 25 mmol) was added to the incomplete reaction and continued stirring at 70 °C for 4 h. Upon completion, the reaction mixture was filtered and washed with MeOH:DCM (1:1) through a pad of diatomaceous earth and the filtrate was concentrated under reduced pressure to afford the crude product. The residue was purified by normal phase chromatography, eluting with 9:1 Pet ether:EtOAc to give the title compound (220 mg, 20% yield). MS m / z 359.0 (M+H).

[0163] The following compound in Table 16 was prepared in a manner essentially analogous to the procedure described in Preparation 117. Table 16: Preparation 118Prep. No.StructureES / MS (m / z) (M+H)Alcohol SM118 303.0 (M-tBu+H)tert-butyl (3-(((2-fluoro-3-(hydroxymeth yl)-4-methylphenyl) amino)methyl) phenyl)carbam ate Preparation 119 S-(3-((tert-Butoxycarbonyl)amino)benzyl) ethanethioate

[0164]

[0165] Dissolved tert-butyl (3-(bromomethyl)phenyl)carbamate (2.0 g, 6.7 mmol) and potassium thioacetate (1.6 g, 14 mmol) in DMF (9 mL, 120 mmol) and stirred at rt under N 2 for 2 h. The reaction was quenched by addition of a satd aq NH 4 Cl (20 mL) and extracted with EtOAc (3 x 30 mL). The combined organic extracts were washed with brine (20 mL), dried with Na 2 SO 4 , filtered, and concentrated under vacuum to give the crude product. The residue was purified by normal phase chromatography, eluting with 17:3 Pet ether:EtOAc to give the title compound (1.8 g, 89% yield). MS m / z 225.9 (M-tBu+H).Preparation 120 Methyl (E)-6-bromo-2-fluoro-3-(4-nitrostyryl)benzoate

[0166]

[0167] To a solution of diethyl (4-nitrobenzyl)phosphonate (1.7 g, 6.1 mmol) and 15-crown-5 (1.3 g, 5.7 mmol) in DMF (30 mL) was added sodium hydride in oil (340 mg, 8.5 mmol, 60 mass%). After stirring at 0 °C for 30 min, methyl 6-bromo-2-fluoro-3-formylbenzoate (1.5 g, 5.7 mmol) was added under N 2 . After 1.5 h, the reaction was quenched by addition of satd aq NH 4 Cl (40 mL) to precipitate a yellow solid. The solid was collected by suction filtration, washed with water, and dried under vaccum to give the title compound (2.2 g, 89% yield). MS m / z 379.9, 381.9 (M+H).Preparation 121 Methyl 3-(4-((tert-butoxycarbonyl)amino)phenethyl)-2-fluoro-6-methylbenzoate

[0168]

[0169] To a solution of methyl (E)-2-fluoro-6-methyl-3-(4-nitrostyryl)benzoate (710 mg, 2.2 mmol) in MeOH (15 mL) was added palladium (650 mg, 0.31 mmol) and di-tert-butyl dicarbonate (0.57 mL, 2.5 mmol). The mixture was stirred at rt for 2 h under H 2 (103,421 Pa = 15 psi)

[0170] The reaction mixture was filtered through a pad of diatomaceous earth and the filtrate was concentrated under reduced pressure to afford the crude product. The residue was purified by normal phase chromatography, eluting with 3:2 Pet ether:EtOAc to give the title compound (620 mg, 69% yield). 1< H NMR (400.21 MHz, DMSO): δ 9.24 (s, 1H), 7.34 (d, J= 8.3 Hz, 2H), 7.26 (t, J= 7.9 Hz, 1H), 7.05 (dd, J= 8.2, 14.8 Hz, 3H), 3.87 (s, 3H), 2.86-2.68 (m, 4H), 2.26 (s, 3H), 1.47 (s, 10H).Preparation 122 tert-Butyl (3-((4-bromo-3-(1,3-dioxolan-2-yl)-2-fluorophenoxy)methyl)phenyl)carbamate

[0171]

[0172] With a Dean-Stark trap attached, a solution of tert-butyl (3-((4-bromo-2-fluoro-3-formylphenoxy)methyl)phenyl)carbamate (1.0 g, 2.5 mmol), ethylene glycol (0.55 mL, 9.8 mmol), and p-toluenesulfonic acid monohydrate (47 mg, 0.25 mmol) in toluene (16 mL, 150 mmol) was refluxed at 135 °C for 1 h. The reaction solution was cooled to rt and diluted with water (15 mL) and EtOAc (25 mL). The phases were separated, and the aqueous was extracted with EtOAc. The combined organic layers were dried with Na 2 SO 4 , filtered, and evaporated to give a crude residue. The residue was purified by normal phase chromatography, eluting with 24:1 DCM:MeOH to give the title compound (1.2 g, 44% yield). MS m / z 486.8 (M+NH 4 ).Alternative Preparation 122 tert-Butyl (3-((4-bromo-3-(1,3-dioxolan-2-yl)-2-fluorophenoxy)methyl)phenyl)carbamate

[0173] With a Dean-Stark trap attached, a solution of 6-bromo-2-fluoro-3-hydroxybenzaldehyde (1.04 g, 4.75 mmol), ethylene glycol (1.1 mL, 20 mmol), and p-toluenesulfonic acid monohydrate (88 mg, 0.46 mmol) in toluene (32 mL) was refluxed at 135 °C for 1 h. The reaction solution was cooled to rt and washed with water (15 mL). The phases were separated. The organic layer was dried with Na 2 SO 4 , filtered, and evaporated to give a crude residue. The residue was purified by normal phase chromatography, eluting with 20:1 DCM:MeOH to give 4-bromo-3-(1,3-dioxolan-2-yl)-2-fluoro-phenol (1.06 g, 4.03 mmol). This material was dissolved in DMF (8.0 mL) and potassium carbonate (1.40 g, 10.1 mmol) was added. This mixture was stirred at rt for 5 min. tert-Butyl 3-(bromomethyl)phenylcarbamate (1.21 g, 4.23 mmol) was then added and the mixture stirred for 75 min. The mixture was then diluted with water (40 mL) and extracted with EtOAc (40 mL). The phases were separated. The organic layer was dried with Na 2 SO 4 , filtered, and evaporated to give a crude residue. The residue was purified by normal phase chromatography, eluting with 3:1 EtOAc:hexanes to give tert-butyl (3-((4-bromo-3-(1,3-dioxolan-2-yl)-2-fluorophenoxy)methyl)phenyl)carbamate (1.72 g, 3.66 mmol, 77% yield). MS m / z 485.0, 487.2 (M+NH 4 ).

[0174] Wherein G 3< is

[0175] Wherein K is hydrogen or methyl.Preparation 123 tert-Butyl (3-((2-fluoro-3-formyl-4-vinylphenoxy)methyl)phenyl)carbamate

[0176]

[0177] tert-Butyl (3-((4-bromo-3-(1,3-dioxolan-2-yl)-2-fluorophenoxy)methyl)phenyl)carbamate (400 mg, 0.85 mmol), potassium vinyltrifluoroborate (0.14 g, 1.0 mmol), and cesium carbonate (0.84 g, 2.6 mmol) were placed in a 25-mL microwave vial that was purged with N 2 . THF (9 mL) and water (1 mL, 56 mmol) were added. The mixture was degassed by bubbling sub-surface N 2 for 5 minutes, palladium(II) acetate (10 mg, 0.04 mmol) was added, and the reaction was heated to 100 °C overnight. The reaction was cooled to rt for 3 days. EtOAc and water were added, the phases were separated, and the aqueous layer was extracted twice with EtOAc. The combined organic layers were dried over Na 2 SO 4 , filtered, and concentrated to a crude residue. The residue was purified by normal phase chromatography, eluting with 3:2 hexanes:EtOAc to give the title compound (320 mg, 16% yield). MS m / z 369.6 (M-H).

[0178] The following compound in Table 17 was prepared in a manner essentially analogous to the procedure described in Preparation 123. Table 17: Preparation 124Prep. No.StructureES / MS (m / z) (M+H)Borate SM124 428.2 (M-H)trifluoro(prop-1-en-2-yl)borate potassium(I) Preparation 125 tert-Butyl N-[3-[[3-(1,3-dioxolan-2-yl)-2-fluoro-4-isopropyl-phenoxy]methyl]phenyl]carbamate

[0179]

[0180] Sulfided 5wt% platinum on carbon (0.057 g, 0.29 mmol) was added to a 70-mL Parr shaker bottle and degassed with N 2 . Added 5 mL EtOAc, then added tert-butyl (3-((3-(1,3-dioxolan-2-yl)-2-fluoro-4-(prop-1-en-2-yl)phenoxy)methyl)phenyl)carbamate (0.231 g, 0.538 mmol) in 6 mL EtOAc to the bottle. The bottle was sealed, purged with N 2 , purged with H 2 , and pressurized to 413,685 Pa (60 psi) H 2 for 5 h at rt. The reaction mixture was filtered and concentrated to give the title compound (255 mg, quant yield). MS m / z 430.4 (M-H).Preparation 126 tert-Butyl (3-((4-cyano-3-(1,3-dioxolan-2-yl)-2-fluorophenoxy)methyl)phenyl)carbamate

[0181]

[0182] In a microwave vial, a mixture of tert-butyl (3-((4-bromo-3-(1,3-dioxolan-2-yl)-2-fluorophenoxy)methyl)phenyl)carbamate (240 mg, 0.50 mmol), zinc cyanide (130 mg, 1.1 mmol), and zinc chloride in THF (1.0 mL, 0.50 mmol, 0.500 mol / L) in DMF (2.5 mL, 32 mmol) was bubbled with N 2 . Tetrakis(triphenylphosphine)palladium(0) (31 mg, 0.03 mmol) was added. The reaction mixture was bubbled with N 2 , capped, and microwaved at 110 °C for 1 h. Additional zinc cyanide (120 mg, 1.0 mmol) and tetrakis(triphenylphosphine)palladium(0) (27 mg, 0.02 mmol) were added. The reaction mixture was bubbled with N 2 , capped, and microwaved at 120 °C for 30 min. The reaction solution was washed with water (15 mL). The organic layer was dried with Na 2 SO 4 , filtered through paper, and rotary evaporated to give crude residue. The residue was purified by normal phase chromatography, eluting with 7:3 hexanes:EtOAc to give the title compound (90 mg, 43% yield). MS m / z 412.6 (M-H).

[0183] In Scheme 17, the compound of structure 1, wherein R is H, is reacted with a compound of structure 2, wherein Pg is a suitable nitrogen protecting group, such as a tert-butyloxy carbonyl, and wherein G is: under conditions well known to one of ordinary skill in the art to provide the compound of Formula I wherein R is hydrogen.

[0184] More specifically, as shown in Scheme 17A below, the compound of structure 1a, wherein R is H, is reacted with the compound of structure 2, wherein Pg and G are defined as above, under conditions well known to one of ordinary skill in the art to provide the compounds of Formula Ib and Formula Ic.

[0185] For example, about 1 equivalent of the compound of structure 1a, wherein R is H, and about 1 equivalent of a compound of structure 2, wherein Pg and G are as defined in Scheme 17, are suspended in a suitable organic solvent, such as acetonitrile. The suspension is cooled to about -10 °C to about -25 °C and then treated with about 5 equivalents of a suitable acid, such as perchloric acid (70% in water) or trifluoroacetic acid. The reaction mixture is then warmed to room temperature and allowed to stir for about 1 to 8 hours. Additional organic solvents may be added, such as acetonitrile and dimethylformamide, and the mixture is allowed to stir for about 2 additional hours. The reaction is then quenched using standard conditions, such as with saturated aqueous sodium bicarbonate and the products are isolated using standard techniques well known in the art, such as extraction with suitable organic solvents, such as methylene chloride:isopranol, drying the organic extracts over magnesium sulfate, filtering, and concentration under vacuum to provide the crude product mixture. This crude mixture can be purified and the products of Formula Ib and Formula Ic separated using techniquest well know in the art, such as chromatography, including for example normal phase chromatography with a suitable eluent, such as MeOH in DCM, and reverse phase chromatography with a suitable eluent, such as 2:1 10 mM ammonium bicarbonate water + 5% methanol:acetonitrile.Example 1 (6aR,6bS,7S,8aS,8bS,10R,11aR,12aS,12bS)-10-(3-((3-Aminobenzyl)oxy)-2-fluoro-6-methylphenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-one

[0186]

[0187] Perchloric acid (70% in water, 4.8 mL) was added to a suspension of (8S,9S,10R,11S,13S,14S,16R,17S)-11,16,17-trihydroxy-17-(2-hydroxyacetyl)-10,13-dimethyl-7,8,9,11,12,14,15,16-octahydro-6H-cyclopenta[a]phenanthren-3-one (4.4 g, 12 mmol, also referred to as "16alpha-hydroxyprednisolone") and tert-butyl N-[3-[(2-fluoro-3-formyl-4-methyl-phenoxy)methyl]phenyl]carbamate (4.0 g, 11 mmol, preparation 4) in acetonitrile (110 mL) at -10 °C and was warmed to rt. After 1 h, DMF (10 mL) was added to the suspension at rt. After 18 h, the reaction was quenched with saturated aqueous sodium bicarbonate and extracted with 9:1 methylene chloride:isopropanol. The organic layers were combined; dried over magnesium sulfate; filtered, and concentrated under reduced pressure to give a residue. The residue was purified by reverse phase chromatography, eluting with 1:1 10 mM ammonium bicarbonate water + 5% methanol:acetonitrile to give the title compound, peak 1 (1.72 g, 25% yield). ES / MS m / z 618.6 (M+H). 1< H NMR (400.13 MHz, d 6 -DMSO) δ 0.93-0.87 (m, 6H), 1.40 (s, 3H), 1.71-1.60 (m, 1H), 1.89-1.76 (m, 4H), 2.18-2.12 (m, 2H), 2.29 (s, 4H), 4.23-4.17 (m, 1H), 4.32-4.30 (m, 1H), 4.50-4.43 (m, 1H), 4.81 (d, J= 3.2 Hz, 1H), 4.98-4.95 (m, 3H), 5.16-5.10 (m, 3H), 5.61 (s, 1H), 5.95 (s, 1H), 6.18-6.15 (m, 1H), 6.53-6.48 (m, 2H), 6.58 (s, 1H), 6.90-6.86 (m, 1H), 6.99 (t, J= 7.7 Hz, 1H), 7.12 (t, J= 8.5 Hz, 1H), 7.33-7.30 (m, 1H).Example 2 (6aR,6bS,7S,8aS,8bS,10S,11aR,12aS,12bS)-10-(3-((3-Aminobenzyl)oxy)-2-fluoro-6-methylphenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-one

[0188]

[0189] From Example 1, the residue was purified by reverse phase chromatography, eluting with 1:1 10 mM ammonium bicarbonate water + 5% methanol:acetonitrile to give the title compound peak 2 (1.24 g, 18% yield). ES / MS m / z 618.6 (M+H). 1< H NMR (400.13 MHz, d 6 -DMSO) δ 1< H NMR (400.13 MHz, DMSO): 0.88 (s, 3H), 1.24-1.12 (m, 2H), 1.40 (s, 3H), 1.69-1.56 (m, 1H), 1.91-1.76 (m, 4H), 2.08-2.01 (m, 2H), 2.22 (s, 3H), 2.39-2.29 (m, 1H), 3.18 (d, J= 5.2 Hz, 1H), 4.12-4.00 (m, 1H), 4.37-4.30 (m, 2H), 4.79 (d, J= 3.1 Hz, 1H), 5.00-4.93 (m, 2H), 5.10-5.06 (m, 3H), 5.31 (d, J= 6.7 Hz, 1H), 5.95 (s, 1H), 6.18 (dd, J= 1.8, 10.1 Hz, 1H), 6.34 (s, 1H), 6.53-6.48 (m, 2H), 6.58 (s, 1H), 6.87 (d, J= 8.5 Hz, 1H), 6.99 (t, J= 7.7 Hz, 1H), 7.09 (t, J= 8.5 Hz, 1H), 7.33 (d, J= 10.1 Hz, 1H).Example 3 (6aR,6bS,7S,8aS,8bS,10S,11aR,12aS,12bS)-10-(3-((3-Aminobenzyl)oxy)-2-fluoro-6-methylphenyl)-7-hydroxy-6a,8a-dimethyl-8b-(2-(((2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)oxy)acetyl)-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-one

[0190]

[0191] (2R,3S,4S,5R,6R)-2-(Acetoxymethyl)-6-(2-((6aR,6bS,7S,8aS,8bS,10S,11aR,12aS,12bS)-10-(3-((3-aminobenzyl)oxy)-2-fluoro-6-methylphenyl)-7-hydroxy-6a,8a-dimethyl-4-oxo-1,2,4,6a,6b,7,8,8a,11a,12,12a,12b-dodecahydro-8bH-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-8b-yl)-2-oxoethoxy)tetrahydro-2H-pyran-3,4,5-triyl triacetate (40 mg, 0.04 mmol, Preparation 5) was added to methanol (2 mL) and potassium carbonate (20 mg, 0.20 mmol). After 1 h, the mixture was loaded onto a diatomaceous earth and was purified by reverse phase chromatography, eluting with 1:2 10 mM ammonium bicarbonate water + 5% methanol:acetonitrile to give the title compound (19 mg, 57% yield). ES / MS m / z 780.4 (M+H). 1< H NMR (500.11 MHz, d 6 -DMSO) δ 0.90 (s, 3H), 1.28-1.27 (m, 2H), 1.41 (s, 3H), 1.72-1.69 (m, 1H), 1.92-1.88 (m, 4H), 2.11-2.10 (m, 2H), 2.22 (s, 3H), 2.40-2.35 (m, 1H), 3.50-3.46 (m, 1H), 3.57-3.53 (m, 1H), 3.64-3.61 (m, 1H), 4.17-4.15 (m, 1H), 4.34-4.32 (m, 1H), 4.43-4.39 (m, 2H), 4.57-4.52 (m, 1H), 4.64-4.62 (m, 1H), 4.75-4.72 (m, 2H), 5.00-4.93 (m, 3H), 5.12-5.08 (m, 2H), 5.31-5.29 (m, 1H), 5.95 (d, J= 0.4 Hz, 1H), 6.20-6.17 (m, 1H), 6.34 (s, 1H), 6.54-6.49 (m, 2H), 6.59 (s, 1H), 6.88 (d, J= 8.5 Hz, 1H), 7.00 (t, J= 7.7 Hz, 1H), 7.12-7.08 (m, 1H), 7.35-7.33 (m, 1H).Example 4 (6aR,6bS,7S,8aS,8bS,10R,11aR,12aS,12bS)-10-(3-((3-Aminobenzyl)oxy)-2-fluoro-6-methoxyphenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-one

[0192]

[0193] To a suspension of tert-butyl (3-((2-fluoro-3-formyl-4-methoxyphenoxy)methyl)phenyl)carbamate (2.6 g, 6.9 mmol, preparation 8) and 16alpha-hydroxyprednisolone (2.5 g, 6.6 mmol) in acetonitrile (100 mL) at -20 °C was added perchloric acid (70% in water, 3.3 mL, 5 equiv) dropwise. The mixture was stirred at - 20 °C for 7 h. The solution was transferred to a separatory funnel. The solution was added dropwise to an aqueous solution of sodium hydroxide (7.5 mL 5N aq NaOH in 1 L water). After the addition was completed, the pH was measured at 5 and the pH was adjusted to 8 with 5N aq NaOH. The suspension was stirred for 10 minutes. The solid was collected by vacuum filtration and the solid was washed with water. The solid was dried on the filter overnight. The solid was purified by reverse phase chromatography, eluting with 1:1 10 mM ammonium bicarbonate water + 5% methanol:acetonitrile to give the title compound, peak 1 (804 mg, 18% yield). MS m / z 634.2 (M+H). 1< H NMR (399.8 MHz, d 6 -DMSO) δ 7.33 (d, J= 10.1 Hz, 1H), 7.17 (t, J= 9.2 Hz, 1H), 6.98 (t, J= 7.8 Hz, 1H), 6.76 (dd, J= 1.0, 9.2 Hz, 1H), 6.56 (d, J= 1.6 Hz, 1H), 6.52-6.48 (m, 2H), 6.17 (dd, J= 1.9, 10.1 Hz, 1H), 5.96 (s, 1H), 5.71 (s, 1H), 5.17 (t, J= 6.0 Hz, 1H), 5.10 (s, 2H), 4.94-4.90 (m, 3H), 4.79 (d, J= 3.1 Hz, 1H), 4.44-4.38 (m, 1H), 4.33-4.31 (m, 1H), 4.22-4.15 (m, 1H), 3.70 (s, 3H), 2.37-2.33 (m, 1H), 2.14-2.04 (m, 2H), 1.96-1.88 (m, 1H), 1.82-1.70 (m, 3H), 1.64-1.56 (m, 1H), 1.41 (s, 3H), 0.86 (s, 5H).Example 5 (6aR,6bS,7S,8aS,8bS,10S,11aR,12aS,12bS)-10-(3-((3-Aminobenzyl)oxy)-2-fluoro-6-methoxyphenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-one

[0194]

[0195] From Example 4, the residue was purified by reverse phase chromatography, eluting with 1:1 10 mM ammonium bicarbonate water + 5% methanol:acetonitrile to give the title compound peak 2 (1.19 g, 27% yield). MS m / z 634.2 (M+H). 1< H NMR (399.8 MHz, d 6 -DMSO) δ 7.32 (d, J= 10.0 Hz, 1H), 7.17-7.12 (m, 1H), 6.99 (t, J= 7.7 Hz, 1H), 6.72 (d, J= 8.8 Hz, 1H), 6.58 (s, 1H), 6.53-6.46 (m, 3H), 6.18 (dd, J= 1.7, 10.1 Hz, 1H), 5.95 (s, 1H), 5.25 (d, J= 6.5 Hz, 1H), 5.10 (s, 2H), 5.00-4.90 (m, 3H), 4.78 (d, J= 3.1 Hz, 1H), 4.37-4.31 (m, 2H), 4.02-3.96 (m, 1H), 3.63 (s, 3H), 2.34-2.31 (m, 1H), 2.11-2.02 (m, 2H), 1.88-1.76 (m, 4H), 1.60-1.54 (m, 1H), 1.40 (s, 3H), 1.23-1.18 (m, 2H), 0.87 (s, 3H).Alternative Preparation of Example 5

[0196] All solid handling steps were handled in a disposable glove bag including charging the flask with 16alpha-hydroxyprednisolone, solid filtration steps and solid transfer steps.

[0197] To a suspension of tert-butyl (3-((2-fluoro-3-formyl-4-methoxyphenoxy)methyl)phenyl)carbamate (25 g, 67 mmol, preparation 8) and 16alpha-hydroxyprednisolone (25 g, 65 mmol) in ACN (1000 mL) at -25 °C in a 2-L round bottom flask was added perchloric acid in water (31 mL, 330 mmol, 10.6 mol / L) dropwise. The mixture was stirred at -20 °C while monitoring the reaction by LCMS. Internal temperature monitoring indicated a small exotherm upon addition of perchloric acid. The internal temperature was kept below -19 °C with dry ice addition. The mixture was kept below -19 °C for 2 h and then was allowed to warm to -10 °C. The mixture split in two and added dropwise to two separate beakers (Beaker 1 and Beaker 2) containing 76 mL of 5 M aq NaOH in 2 L of water, each. A solid formed upon addition and complete quench of perchloric acid was tested (pH 10). The sticky solid from each addition was transferred and combined to a third beaker (Beaker 3) containing 10% MeOH in DCM. The mixture was stirred until the sticky solid completely dissolved. The remaining solutions (Beaker 1 and Beaker 2) were then filtered through paper to collect residual solids. The isolated solids were rinsed with water and transferred to Beaker 3. Beaker 3 was stirred until all solids were dissolved. The solution was dried for 2 h with Na 2 SO 4 , filtered and evaporated to give a tan foam. The filtrates from the solid collection were extracted with three portions 10% IPA in DCM. The combined organic extracts were dried over Na 2 SO 4 with stirring overnight, then filtered and evaporated to give additional crude residue. The crude products were dissovled in 150 mL 1% MeOH in DCM and purified by normal phase chromatography using 0-5% MeOH in DCM to give a solid. It was diluted with 600 mL EtOH and spun on the rotary evaporator at 45 °C for 5 minutes. The heat bath was turned up to 60 °C. When the heat bath reached 60 °C it was turned off and the flask spun until the bath reached rt. The flask was taken off the rotary evaporator, capped and allowed to stand overnight at room temperature.

[0198] The solid was collected by vacuum filtration in a glove bag. The solids were rinsed with EtOH and dried on the filter for 5 h. The solid redissolved in 20% EtOH in DCM (1.5 L). Additional DCM was added to achieve a near clear solution (some haze persisted). Solvent exchange was achieved by rotary evaporation at 450 mbar and 45 °C to remove DCM. Once distillation had stopped, the pressure was decreased to 100 mbar to bring off EtOH to approximately 600 mL. The mixture was removed from the rotary evaporator and allowed to stand for 5 h at rt. The solid was collected by vacuum filtration and the solids washed twice with additional EtOH. The filter cake was dried in a vacuum oven at rt for 48 h to give the title compound (42 g, 38% yield). MS m / z 634.6 (M+H).Structural assignment by NMR

[0199]

[0200] Two dimensional through-space ROE NMR analysis of acetal isomers consistently gave a cross peak for H22 (acetal) and H16 in the R configuration. Alternatively, H22 in the S configuration consistently gave about 1 ppm larger shift. All other compounds were assigned essentially by the same method.

[0201] The following compounds in Table 18a were prepared in a manner essentially analogous to the procedures described in Examples 1 to 4 utilizing the corresponding starting material of structure 1a and starting material of structure 2 as prepared in the corresponding preparations and tables 2-17 described above or prepared using standard procedures well known to one of ordinary skill in the art. Purification of final products was performed essentially by the following methods: A. C18 column using eluent 10mM NH 4 HCO 3 in water + 5% MeOH:ACN B. C18 column using eluent 0.1% FA in water:ACN C. SFC Chiralpak AY using eluent EtOH + 0.05% DEA:CO 2 D. Chiralpak IC using eluent MeOH + 0.2% IPAm E. SFC Lux Amylose-2 using eluent IPA + 0.5% DMEA:CO 2 F. SFC Chiralpak AD-H using eluent IPA + 0.5% DMEA:CO 2 G. Chiralpak IC using eluent EtOH + 0.1% NH 3 H 2 O:heptane H. SFC Chiralpack AD using eluent IPA + 0.1% NH 3 H 2 O:CO 2 I. Chiralcel IH using eluent EtOH+ACN (0.1% DEA):heptane J. SFC Chiralpak AD using eluent EtOH + 0.5% DEA:CO 2 K. Chiralpak IE using eluent EtOH + 0.1% NH 3 H 2 O:ACN L. Chiralpak AD-H using eluent EtOH:ACN + 0.2% IPAm M. Chiralpak AD-H using eluent EtOH:ACN N. SFC Chiralpak IC using eluent EtOH + 0.05% DMEA:CO 2 O. SFC Chiralcel OJ-H using eluent MeOH + 0.5% DMEA:CO 2 Table 18a: Examples 6-158 (structures) Ex No.StructureES / MS (m / z) (M+H)Purification method *6 570.4A7 570.4A8 570.4A9 570.4A10 571.4B11 570.4B12 572.2A13 572.2A14 572.2A15 572.2A16 600.2A17 600.2A18 600.2A19 586.2A20 586.2A21 604.2A22 604.2A, O23 620.2A24 620.2A25 620.2A26 620.2A27 620.2A28 620.2A29 604.2A30 604.2A31 620.4M32 620.4M33 556.2A34 556.2A35 600.2A36 600.2A37 604.2A38 604.2A39 556.2A40 556.2A41 638.4A, L42 586.4A, L43 638.4A, L44 586.4A, L45 604.4A, O46 604.4A, O47 638.2A48 638.2A49 622.3A50 622.3A51 620.5A, O52 620.5A, O53 588.2A54 588.2A55 617.5B, C56 618.4A57 618.4A58 622.0A59 622.4A60 634.3A61 634.3A62 632.4A63 632.4A64 617.6B, J65 634.5B66 634.5B67 618.5B, I68 618.5B69 617.5B70 617.0B, K71 634.5A, G72 634.1B, H73 617.5B, C74 670.4A75 632.2A76 632.2A77 604.4A78 604.3A79 670.4A80 600.6A81 600.6A82 622.4A83 622.3A84 632.4B, H85 632.4A86 631.5B,G87 616.5B88 616.4A89 616.4A90 616.4A91 616.6A92 664.4A93 664.4A94 638.4D95 638.4D96 618.6N97 618.6N98 600.2B99 600.2B100 634.4A101 634.4A102 634.5B, H103 634.5B, G104 617.1B, K105 617.5B106 618.5B107 618.5B, I108 634.5B109 634.5B110 617.6B, J111 632.2A112 631.4B, G113 616.5B114 632.4B, H115 602.2A116 602.2A117 682.2A118 682.2A119 666.4F120 616.4A121 616.4A122 680.6B123 679.8B124 711.6A125 712.0A126 667.8B127 597.8A128 597.8A129 614.6F130 614.6F131 651.8B132 651.8B133 630.4A134 630.4A135 613.6E136 613.6E137 666.4F138 646.4A139 646.4A140 638.1A141 604.4A142 604.4A143 622.2A144 651.8B145 651.8B146 622.0A147 634.2A148 634.4A149 606.4A150 644.4A151 644.4A152 662.4A153 662.4A154 634.5B155 630.4A156 630.4A157 606.4A158 634.5B Table 18b: Examples 6-158 (chemical names) Ex No.Chemical Name6(6aR,6bS,7S,8aS,8bS,10R,11aR,12aS,12bS)-10-(3-(4-aminobenzyl)phenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-one7(6aR,6bS,7S,8aS,8bS,10S,11aR,12aS,12bS)-10-(3-(4-aminobenzyl)phenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-0one8(6aR,6bS,7S,8aS,8bS,10R,11aR,12aS,12bS)-10-(3-(3-aminobenzyl)phenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-0one9(6aR,6bS,7S,8aS,8bS,10S,11aR,12aS,12bS)-10-(3-(3-aminobenzyl)phenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-0one10(6aR,6bS,7S,8aS,8bS,10R,11aR,12aS,12bS)-10-(3-(2-aminobenzyl)phenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-0one11(6aR,6bS,7S,8aS,8bS,10S,11aR,12aS,12bS)-10-(3-(2-aminobenzyl)phenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-0one12(6aR,6bS,7S,8aS,8bS,10R,11aR,12aS,12bS)-10-(3-(4-aminophenoxy)phenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-0one13(6aR,6bS,7S,8aS,8bS,10S,11aR,12aS,12bS)-10-(3-(4-aminophenoxy)phenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-0one14(6aR,6bS,7S,8aS,8bS,10R,11aR,12aS,12bS)-10-(3-(3-aminophenoxy)phenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-0one15(6aR,6bS,7S,8aS,8bS,10S,11aR,12aS,12bS)-10-(3-(3-aminophenoxy)phenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-0one16(6aR,6bS,7S,8aS,8bS,10R,11aR,12aS,12bS)-10-(3-((3-aminobenzyl)oxy)-2-methylphenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-0one17(6aR,6bS,7S,8aS,8bS,10R,11aR,12aS,12bS)-10-(5-((3-aminobenzyl)oxy)-2-methylphenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-0one18(6aR,6bS,7S,8aS,8bS,10S,11aR,12aS,12bS)-10-(5-((3-aminobenzyl)oxy)-2-methylphenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-0one19(6aR,6bS,7S,8aS,8bS,10R,11aR,12aS,12bS)-10-(3-((3-aminobenzyl)oxy)phenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-one20(6aR,6bS,7S,8aS,8bS,10S,11aR,12aS,12bS)-10-(3-((3-aminobenzyl)oxy)phenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-one21(6aR,6bS,7S,8aS,8bS,10RS,11aR,12aS,12bS)-10-(5-((3-aminobenzyl)oxy)-2-fluorophenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-one22(6aR,6bS,7S,8aS,8bS,10S,11aR,12aS,12bS)-10-(5-((3-aminobenzyl)oxy)-2-fluorophenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-0one23(6aR,6bS,7S,8aS,8bS,10R,11aR,12aS,12bS)-10-(3-((3-aminobenzyl)oxy)-4-chlorophenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-0one24(6aR,6bS,7S,8aS,8bS,10S,11aR,12aS,12bS)-10-(3-((3-aminobenzyl)oxy)-4-chlorophenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-0one25(6aR,6bS,7S,8aS,8bS,10R,11aR,12aS,12bS)-10-(3-((3-aminobenzyl)oxy)-5-chlorophenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-0one26(6aR,6bS,7S,8aS,8bS,10S,11aR,12aS,12bS)-10-(3-((3-aminobenzyl)oxy)-5-chlorophenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-0one27(6aR,6bS,7S,8aS,8bS,10R,11aR,12aS,12bS)-10-(5-((3-aminobenzyl)oxy)-2-chlorophenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-0one28(6aR,6bS,7S,8aS,8bS,10S,11aR,12aS,12bS)-10-(5-((3-aminobenzyl)oxy)-2-chlorophenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-0one29(6aR,6bS,7S,8aS,8bS,10R,11aR,12aS,12bS)-10-(3-((3-aminobenzyl)oxy)-5-fluorophenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-0one30(6aR,6bS,7S,8aS,8bS,10S,11aR,12aS,12bS)-10-(3-((3-aminobenzyl)oxy)-5-fluorophenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-0one31(6aR,6bS,7S,8aS,8bS,10R,11aR,12aS,12bS)-10-(3-((3-aminobenzyl)oxy)-2-chlorophenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-0one32(6aR,6bS,7S,8aS,8bS,10S,11aR,12aS,12bS)-10-(3-((3-aminobenzyl)oxy)-2-chlorophenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-0one33(6aR,6bS,7S,8aS,8bS,10R,11aR,12aS,12bS)-10-(3'-amino-[1,1'-biphenyl]-3-yl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-0one34(6aR,6bS,7S,8aS,8bS,10S,11aR,12aS,12bS)-10-(3'-amino-[1,1'-biphenyl]-3-yl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-0one35(6aR,6bS,7S,8aS,8bS,10R,11aR,12aS,12bS)-10-(3-((3-aminobenzyl)oxy)-5-methylphenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-0one36(6aR,6bS,7S,8aS,8bS,10S,11aR,12aS,12bS)-10-(3-((3-aminobenzyl)oxy)-5-methylphenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-0one37(6aR,6bS,7S,8aS,8bS,10R,11aR,12aS,12bS)-10-(3-((3-aminobenzyl)oxy)-2-fluorophenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-0one38(6aR,6bS,7S,8aS,8bS,10S,11aR,12aS,12bS)-10-(3-((3-aminobenzyl)oxy)-2-fluorophenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-0one39(6aR,6bS,7S,8aS,8bS,10R,11aR,12aS,12bS)-10-(4'-amino-[1,1'-biphenyl]-3-yl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-0one40(6aR,6bS,7S,8aS,8bS,10S,11aR,12aS,12bS)-10-(4'-amino-[1,1'-biphenyl]-3-yl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-0one41(6aR,6bS,7S,8aS,8bS,10S,11aR,12aS,12bS)-10-(3-((3-aminobenzyl)oxy)-2-chloro-6-fluorophenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-0one42(6aR,6bS,7S,8aS,8bS,10R,11aR,12aS,12bS)-10-(2-((3-aminobenzyl)oxy)phenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-one43(6aR,6bS,7S,8aS,8bS,10R,11aR,12aS,12bS)-10-(3-((3-aminobenzyl)oxy)-2-chloro-6-fluorophenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-one44(6aR,6bS,7S,8aS,8bS,10S,11aR,12aS,12bS)-10-(2-((3-aminobenzyl)oxy)phenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-one45(6aR,6bS,7S,8aS,8bS,10S,11aR,12aS,12bS)-10-(2-((3-aminobenzyl)oxy)-6-fluorophenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-one46(6aR,6bS,7S,8aS,8bS,10R,11aR,12aS,12bS)-10-(2-((3-aminobenzyl)oxy)-6-fluorophenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-one47(6aR,6bS,7S,8aS,8bS,10R,11aR,12aS,12bS)-10-(3-((3-aminobenzyl)oxy)-6-chloro-2-fluorophenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-one48(6aR,6bS,7S,8aS,8bS,10S,11aR,12aS,12bS)-10-(3-((3-aminobenzyl)oxy)-6-chloro-2-fluorophenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-one49(6aR,6bS,7S,8aS,8bS,10R,11aR,12aS,12bS)-10-(3-((3-aminobenzyl)oxy)-2,6-difluorophenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-one50(6aR,6bS,7S,8aS,8bS,10S,11aR,12aS,12bS)-10-(3-((3-aminobenzyl)oxy)-2,6-difluorophenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-one51(6aR,6bS,7S,8aS,8bS,10R,11aR,12aS,12bS)-10-(2-((3-aminobenzyl)oxy)-6-chlorophenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-one52(6aR,6bS,7S,8aS,8bS,10S,11aR,12aS,12bS)-10-(2-((3-aminobenzyl)oxy)-6-chlorophenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-one53(6aR,6bS,7S,8aS,8bS,10R,11aR,12aS,12bS)-10-(5-(4-aminobenzyl)-2-fluorophenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-one54(6aR,6bS,7S,8aS,8bS,10S,11aR,12aS,12bS)-10-(5-(4-aminobenzyl)-2-fluorophenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-one55(6aR,6bS,7S,8aS,8bS,10S,11aR,12aS,12bS)-10-(3-((3-aminobenzyl)amino)-2-fluoro-6-methylphenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-one56(6aR,6bS,7S,8aS,8bS,10S,11aR,12aS,12bS)-10-(3-((2-aminobenzyl)oxy)-2-fluoro-6-methylphenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-one57(6aR,6bS,7S,8aS,8bS,10R,11aR,12aS,12bS)-10-(3-((2-aminobenzyl)oxy)-2-fluoro-6-methylphenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-one58(6aR,6bS,7S,8aS,8bS,10S,11aR,12aS,12bS)-10-(3-((3-aminobenzyl)oxy)-2,4-difluorophenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-one59(6aR,6bS,7S,8aS,8bS,10R,11aR,12aS,12bS)-10-(3-((3-aminobenzyl)oxy)-2,4-difluorophenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-one60(6aR,6bS,7S,8aS,8bS,10R,11aR,12aS,12bS)-10-(3-((3-aminobenzyl)oxy)-6-fluoro-2-methoxyphenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-one61(6aR,6bS,7S,8aS,8bS,10S,11aR,12aS,12bS)-10-(3-((3-aminobenzyl)oxy)-6-fluoro-2-methoxyphenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-one62(6aR,6bS,7S,8aS,8bS,10S,11aR,12aS,12bS)-10-(3-((2-(aminomethyl)benzyl)oxy)-2-fluoro-6-methylphenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-one63(6aR,6bS,7S,8aS,8bS,10R,11aR,12aS,12bS)-10-(3-((2-(aminomethyl)benzyl)oxy)-2-fluoro-6-methylphenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-one64(6aR,6bS,7S,8aS,8bS,10S,11aR,12aS,12bS)-10-(3-((2-aminobenzyl)amino)-2-fluoro-6-methylphenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-one65(6aR,6bS,7S,8aS,8bS,10S,11aR,12aS,12bS)-10-(3-((2-aminobenzyl)thio)-2-fluoro-6-methylphenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-one66(6aR,6bS,7S,8aS,8bS,10S,11aR,12aS,12bS)-10-(3-((3-aminobenzyl)thio)-2-fluoro-6-methylphenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-one67(6aR,6bS,7S,8aS,8bS,10S,11aR,12aS,12bS)-10-(3-((2-aminophenoxy)methyl)-2-fluoro-6-methylphenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-one68(6aR,6bS,7S,8aS,8bS,10S,11aR,12aS,12bS)-10-(3-((3-aminophenoxy)methyl)-2-fluoro-6-methylphenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-one69(6aR,6bS,7S,8aS,8bS,10S,11aR,12aS,12bS)-10-(3-(((3-aminophenyl)amino)methyl)-2-fluoro-6-methylphenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-one70(6aR,6bS,7S,8aS,8bS,10S,11aR,12aS,12bS)-10-(3-(((2-aminophenyl)amino)methyl)-2-fluoro-6-methylphenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-one71(6aR,6bS,7S,8aS,8bS,10S,11aR,12aS,12bS)-10-(3-(((2-aminophenyl)thio)methyl)-2-fluoro-6-methylphenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-one72(6aR,6bS,7S,8aS,8bS,10S,11aR,12aS,12bS)-10-(3-(((3-aminophenyl)thio)methyl)-2-fluoro-6-methylphenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-one73(6aR,6bS,7S,8aS,8bS,10R,11aR,12aS,12bS)-10-(3-((3-aminobenzyl)amino)-2-fluoro-6-methylphenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-one74(6aR,6bS,7S,8aS,8bS,10R,11aR,12aS,12bS)-10-(5-((3-aminobenzyl)oxy)-2-(trifluoromethoxy)phenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-one75(6aR,6bS,7S,8aS,8bS,10S,11aR,12aS,12bS)-10-(3-((3-(aminomethyl)benzyl)oxy)-2-fluoro-6-methylphenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-one76(6aR,6bS,7S,8aS,8bS,10R,11aR,12aS,12bS)-10-(3-((3-(aminomethyl)benzyl)oxy)-2-fluoro-6-methylphenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-one77(6aR,6bS,7S,8aS,8bS,10R,11aR,12aS,12bS)-10-(3-((2-aminobenzyl)oxy)-2-fluorophenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-one78(6aR,6bS,7S,8aS,8bS,10S,11aR,12aS,12bS)-10-(3-((2-aminobenzyl)oxy)-2-fluorophenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-one79(6aR,6bS,7S,8aS,8bS,10S,11aR,12aS,12bS)-10-(5-((3-aminobenzyl)oxy)-2-(trifluoromethoxy)phenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-one80(6aR,6bS,7S,8aS,8bS,10R,11aR,12aS,12bS)-10-(5-((2-aminobenzyl)oxy)-2-methylphenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-one81(6aR,6bS,7S,8aS,8bS,10S,11aR,12aS,12bS)-10-(5-((2-aminobenzyl)oxy)-2-methylphenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-one82(6aR,6bS,7S,8aS,8bS,10R,11aR,12aS,12bS)-10-(3-((2-aminobenzyl)oxy)-2,6-difluorophenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-one83(6aR,6bS,7S,8aS,8bS,10S,11aR,12aS,12bS)-10-(3-((2-aminobenzyl)oxy)-2,6-difluorophenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-one84(6aR,6bS,7S,8aS,8bS,10S,11aR,12aS,12bS)-10-(3-(4-aminophenethoxy)-2-fluoro-6-methylphenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-one85(6aR,6bS,7S,8aS,8bS,10S,11aR,12aS,12bS)-10-(3-(3-aminophenethoxy)-2-fluoro-6-methylphenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-one86(6aR,6bS,7S,8aS,8bS,10S,11aR,12aS,12bS)-10-(3-((3-aminobenzyl)(methyl)amino)-2-fluoro-6-methylphenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-one87(6aR,6bS,7S,8aS,8bS,10S,11aR,12aS,12bS)-10-(3-(4-aminophenethyl)-2-fluoro-6-methylphenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-one88(6aR,6bS,7S,8aS,8bS,10R,11aR,12aS,12bS)-10-(5-((3-aminobenzyl)oxy)-2-methoxyphenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-one89(6aR,6bS,7S,8aS,8bS,10S,11aR,12aS,12bS)-10-(5-((3-aminobenzyl)oxy)-2-methoxyphenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-one90(6aR,6bS,7S,8aS,8bS,10R,11aR,12aS,12bS)-10-(3-((3-aminobenzyl)oxy)-2-methoxyphenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-one91(6aR,6bS,7S,8aS,8bS,10S,11aR,12aS,12bS)-10-(3-((3-aminobenzyl)oxy)-2-methoxyphenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-one92(6aR,6bS,7S,8aS,8bS,10R,11aR,12aS,12bS)-10-(5-((3-aminobenzyl)oxy)-2-bromophenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-one93(6aR,6bS,7S,8aS,8bS,10S,11aR,12aS,12bS)-10-(5-((3-aminobenzyl)oxy)-2-bromophenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-one94(6aR,6bS,7S,8aS,8bS,10R,11aR,12aS,12bS)-10-(3-((2-aminobenzyl)oxy)-2-chloro-6-fluorophenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-one95(6aR,6bS,7S,8aS,8bS,10S,11aR,12aS,12bS)-10-(3-((2-aminobenzyl)oxy)-2-chloro-6-fluorophenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-one96(6aR,6bS,7S,8aS,8bS,10R,11aR,12aS,12bS)-10-(3-((3-aminobenzyl)oxy)-6-fluoro-2-methylphenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-one97(6aR,6bS,7S,8aS,8bS,10S,11aR,12aS,12bS)-10-(3-((3-aminobenzyl)oxy)-6-fluoro-2-methylphenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-one98(6aR,6bS,7S,8aS,8bS,10R,11aR,12aS,12bS)-10-(3-((2-aminobenzyl)oxy)-2-methylphenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-one99(6aR,6bS,7S,8aS,8bS,10S,11aR,12aS,12bS)-10-(3-((2-aminobenzyl)oxy)-2-methylphenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-one100(6aR,6bS,7S,8aS,8bS,10R,11aR,12aS,12bS)-10-(3-((2-aminobenzyl)oxy)-2-fluoro-6-methoxyphenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-one101(6aR,6bS,7S,8aS,8bS,10S,11aR,12aS,12bS)-10-(3-((2-aminobenzyl)oxy)-2-fluoro-6-methoxyphenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-one102(6aR,6bS,7S,8aS,8bS,10R,11aR,12aS,12bS)-10-(3-(((3-aminophenyl)thio)methyl)-2-fluoro-6-methylphenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl- 1,2,6a,6b,7,8,8a,8b, I I a, 12,12a, 12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-one103(6aR,6bS,7S,8aS,8bS,10R,1aR,12aS,12bS)-10-(3-(((2-aminophenyl)thio)methyl)-2-fluoro-6-methylphenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-one104(6aR,6bS,7S,8aS,8bS,10R,11aR,12aS,12bS)-10-(3-(((2-aminophenyl)amino)methyl)-2-fluoro-6-methylphenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-one105(6aR,6bS,7S,8aS,8bS,10R,11aR,12aS,12bS)-10-(3-(((3-aminophenyl)amino)methyl)-2-fluoro-6-methylphenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-one106(6aR,6bS,7S,8aS,8bS,10R,11aR,12aS,12bS)-10-(3-((3-aminophenoxy)methyl)-2-fluoro-6-methylphenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-one107(6aR,6bS,7S,8aS,8bS,10R,11aR,12aS,12bS)-10-(3-((2-aminophenoxy)methyl)-2-fluoro-6-methylphenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-one108(6aR,6bS,7S,8aS,8bS,10R,11aR,12aS,12bS)-10-(3-((3-aminobenzyl)thio)-2-fluoro-6-methylphenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-one109(6aR,6bS,7S,8aS,8bS,10R,11aR,12aS,12bS)-10-(3-((2-aminobenzyl)thio)-2-fluoro-6-methylphenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-one110(6aR,6bS,7S,8aS,8bS,10R,11aR,12aS,12bS)-10-(3-((2-aminobenzyl)amino)-2-fluoro-6-methylphenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-one111(6aR,6bS,7S,8aS,8bS,10R,11aR,12aS,12bS)-10-(3-(3-aminophenethoxy)-2-fluoro-6-methylphenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-one112(6aR,6bS,7S,8aS,8bS,10R,11aR,12aS,12bS)-10-(3-((3-aminobenzyl)(methyl)amino)-2-fluoro-6-methylphenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-one113(6aR,6bS,7S,8aS,8bS,10R,11aR,12aS,12bS)-10-(3-(4-aminophenethyl)-2-fluoro-6-methylphenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-one114(6aR,6bS,7S,8aS,8bS,10R,11aR,12aS,12bS)-10-(3-(4-aminophenethoxy)-2-fluoro-6-methylphenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-one115(6aR,6bS,7S,8aS,8bS,10S,11aR,12aS,12bS)-10-(5-(4-aminophenoxy)-2-methoxyphenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-one116(6aR,6bS,7S,8aS,8bS,10S,11aR,12aS,12bS)-10-(5-(3-aminophenoxy)-2-methoxyphenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-one117(6aR,6bS,7S,8aS,8bS,10R,11aR,12aS,12bS)-10-(3-((3-aminobenzyl)oxy)-6-bromo-2-fluorophenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-one118(6aR,6bS,7S,8aS,8bS,10S,11aR,12aS,12bS)-10-(3-((3-aminobenzyl)oxy)-6-bromo-2-fluorophenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-one119(6aR,6bS,7S,8aS,8bS,10R,11aR,12aS,12bS)-10-(3-((3-aminobenzyl)oxy)-2-bromophenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-one (6aR,6bS,7S,8aS,8bS,10R,11aR,12aS,12bS)-10-(5-((2-aminobenzyl)oxy)-2-methoxyphenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-one (6aR,6bS,7S,8aS,8bS,10S,11aR,12aS,12bS)-10-(5-((2-aminobenzyl)oxy)-2-methoxyphenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-one120121122(6aR,6bS,7S,8aS,8bS,10R,11aR,12aS,12bS)-10-(4-((3-aminobenzyl)oxy)-3-fluoro-[1,1'-biphenyl]-2-yl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-one123(6aR,6bS,7S,8aS,8bS,10S,11aR,12aS,12bS)-10-(4-((3-aminobenzyl)oxy)-3-fluoro-[1,1'-biphenyl]-2-yl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-one124(6aR,6bS,7S,8aS,8bS,10R,11aR,12aS,12bS)-10-(5-((3-aminobenzyl)oxy)-2-iodophenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-one125(6aR,6bS,7S,8aS,8bS,10S,11aR,12aS,12bS)-10-(5-((3-aminobenzyl)oxy)-2-iodophenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-one126(6aR,6bS,7S,8aS,8bS,10S,11aR,12aS,12bS)-10-(5-((3-aminobenzyl)oxy)-2-(thiophen-2-yl)phenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-one127(6aR,6bS,7S,8aS,8bS,10R,11aR,12aS,12bS)-10-(3-((3-aminophenyl)ethynyl)-2-fluorophenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-one128(6aR,6bS,7S,8aS,8bS,10S,11aR,12aS,12bS)-10-(3-((3-aminophenyl)ethynyl)-2-fluorophenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-one129(6aR,6bS,7S,8aS,8bS,10R,11aR,12aS,12bS)-10-(3-((3-aminobenzyl)oxy)-2,6-dimethylphenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-one130(6aR,6bS,7S,8aS,8bS,10S,11aR,12aS,12bS)-10-(3-((3-aminobenzyl)oxy)-2,6-dimethylphenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-one131(6aR,6bS,7S,8aS,8bS,10R,11aR,12aS,12bS)-10-(5-((3-aminobenzyl)oxy)-2-(furan-3-yl)phenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-one132(6aR,6bS,7S,8aS,8bS,10S,11aR,12aS,12bS)-10-(5-((3-aminobenzyl)oxy)-2-(furan-3-yl)phenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-one133(6aR,6bS,7S,8aS,8bS,10R,11aR,12aS,12bS)-10-(5-((3-aminobenzyl)oxy)-2-ethoxyphenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-one134(6aR,6bS,7S,8aS,8bS,10S,11aR,12aS,12bS)-10-(5-((3-aminobenzyl)oxy)-2-ethoxyphenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-one135(6aR,6bS,7S,8aS,8bS,10R,11aR,12aS,12bS)-10-(3-((3-aminobenzyl)amino)-2,6-dimethylphenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-one136(6aR,6bS,7S,8aS,8bS,10S,11aR,12aS,12bS)-10-(3-((3-aminobenzyl)amino)-2,6-dimethylphenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl- 1,2,6a,6b,7,8,8a,8b, I I a, 12,12a, 12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-one137(6aR,6bS,7S,8aS,8bS,10S,11aR,12aS,12bS)-10-(3-((3-aminobenzyl)oxy)-2-bromophenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-one138(6aR,6bS,7S,8aS,8bS,10R,11aR,12aS,12bS)-10-(3-((3-aminobenzyl)oxy)-2-fluoro-6-isopropylphenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-one139(6aR,6bS,7S,8aS,8bS,10S,11aR,12aS,12bS)-10-(3-((3-aminobenzyl)oxy)-2-fluoro-6-isopropylphenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-one140(6aR,6bS,7S,8aS,8bS,10S,11aR,12aS,12bS)-10-(3-((2-aminobenzyl)oxy)-6-chloro-2-fluorophenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-one141(6aR,6bS,7S,8aS,8bS,10S,11aR,12aS,12bS)-10-(5-(3-aminobenzyl)-2-chlorophenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-one142(6aR,6bS,7S,8aS,8bS,10S,11aR,12aS,12bS)-10-(5-(4-aminobenzyl)-2-chlorophenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-one143(6aR,6bS,7S,8aS,8bS,10S,11aR,12aS,12bS)-10-(3-(3-aminobenzyl)-6-chloro-2-fluorophenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-one144(6aR,6bS,7S,8aS,8bS,10R,11aR,12aS,12bS)-10-(5-((3-aminobenzyl)oxy)-2-(furan-2-yl)phenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-one145(6aR,6bS,7S,8aS,8bS,10S,11aR,12aS,12bS)-10-(5-((3-aminobenzyl)oxy)-2-(furan-2-yl)phenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-one146(6aR,6bS,7S,8aS,8bS,10S,11aR,12aS,12bS)-10-(3-(4-aminobenzyl)-6-chloro-2-fluorophenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-one147(6aR,6bS,7S,8aS,8bS,10R,11aR,12aS,12bS)-10-(3-((3-aminobenzyl)oxy)-2-fluoro-4-methoxyphenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-one148(6aR,6bS,7S,8aS,8bS,10S,11aR,12aS,12bS)-10-(3-((3-aminobenzyl)oxy)-2-fluoro-4-methoxyphenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-one149(6aR,6bS,7S,8aS,8bS,10S,11aR,12aS,12bS)-10-(3-(3-aminobenzyl)-2,6-difluorophenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-one150(6aR,6bS,7S,8aS,8bS,10R,11aR,12aS,12bS)-10-(3-((3-aminobenzyl)oxy)-6-cyclopropyl-2-fluorophenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-one151(6aR,6bS,7S,8aS,8bS,10S,11aR,12aS,12bS)-10-(3-((3-aminobenzyl)oxy)-6-cyclopropyl-2-fluorophenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-one152(6aR,6bS,7S,8aS,8bS,10R,11aR,12aS,12bS)-10-(4-((3-aminobenzyl)oxy)-[1,1'-biphenyl]-2-yl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-one153(6aR,6bS,7S,8aS,8bS,10S,11aR,12aS,12bS)-10-(4-((3-aminobenzyl)oxy)-[1,1'-biphenyl]-2-yl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-one154(6aR,6bS,7S,8aS,8bS,10S,11aR,12aS,12bS)-10-(3-((3-aminobenzyl)thio)-2-fluoro-4-methylphenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-one155(6aR,6bS,7S,8aS,8bS,10R,11aR,12aS,12bS)-10-(3-((3-aminobenzyl)oxy)-2-fluoro-6-vinylphenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-one156(6aR,6bS,7S,8aS,8bS,10S,11aR,12aS,12bS)-10-(3-((3-aminobenzyl)oxy)-2-fluoro-6-vinylphenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-one157(6aR,6bS,7S,8aS,8bS,10R,11aR,12aS,12bS)-10-(3-(3-aminobenzyl)-2,6-difluorophenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-one158(6aR,6bS,7S,8aS,8bS,10R,11aR,12aS,12bS)-10-(3-((3-aminobenzyl)thio)-2-fluoro-4-methylphenyl)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-one Example 159 4-((3-Aminobenzyl)oxy)-3-fluoro-2-((6aR,6bS,7S,8aS,8bS,10S,11aR,12aS,12bS)-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a-dimethyl-4-oxo-2,4,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-1H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-10-yl)benzonitrile

[0202]

[0203] Trifluoromethanesulfonic acid (920 µL, 10 mmol) was added dropwise to a suspension of 16alpha-hydroxyprednisolone (140 mg, 0.36 mmol) and tert-butyl (3-((4-cyano-3-(1,3-dioxolan-2-yl)-2-fluorophenoxy)methyl)phenyl)carbamate (140 mg, 0.34 mmol) in ACN (5 mL, 95 mmol) at 0 °C. The reaction was quenched with satd aq NaHCO 3 and extracted with 10% IPA in DCM. The combined organic layers were dried with MgSO 4 , filtered, and concentrated to a crude residue. The crude residue was purified by reverse phase purification, eluting with 1:1 10mM NH 4 HCO 3 in water + 5% MeOH:ACN to give the title compound (12 mg, 6% yield). MS m / z 630.0 (M+H). 1< H NMR (400.13 MHz, d 6 -DMSO) δ 7.70-7.67 (m, 1H), 7.45-7.41 (m, 1H), 7.33 (d, J= 10.1 Hz, 1H), 7.04-7.00 (m, 1H), 6.61-6.51 (m, 3H), 6.45 (s, 1H), 6.20-6.17 (m, 1H), 5.95 (s, 1H), 5.37-5.35 (m, 1H), 5.15 (s, 4H), 4.86-4.84 (m, 1H), 4.32-4.31 (m, 2H), 4.07-4.01 (m, 1H), 2.14-2.12 (m, 2H), 1.92-1.88 (m, 4H), 1.67-1.66 (m, 1H), 1.40-1.39 (m, 3H), 1.25-1.20 (m, 2H), 0.89-0.88 (m, 3H).hGR CoActivator Recruitment Assay

[0204] The activity of glucocorticoid compounds was measured using the LanthaScreen TR-Fret GR Coactivator Assay from Life Technologies (A15899). The compounds were acoustically transferred to an assay plate in a 3-fold 10-point serial dilution with a top concentration of 200 nM. Ten microliters of a 2x solution of GR-LBD was added to the compound plate and incubated for 10 min. Then ten microliters of a 2x solution of Fluoresein-SRC1-4 and Tb labelled anti-GST antibody were added to the plate. The plate was incubated in the dark for two hours and then read on an Envision plate reader, with excitation at 340 nm and emission at 520 nm (Fluorescein) and 490 nm (Terbium). The emission ratio of 520 / 490 was analyzed in Genedata. To obtain percent activity, the data was compared to a negative control of DMSO and positive control of 4uM dexamethasone. The following exemplified compounds were tested following the procedure as essentially described above and exhibited the following activity as listed in Table 19. Table 19: In vitro potency of compounds of Examples 1, 2, 4, and 5 in the hGR CoActivator Recruitment AssayExample No. IC 50 (nM) 12.1221.4442.4751.40

[0205] The compounds of Examples 6-44, 46-51, 53-79, and 81-158 provided a relative IC 50 of less than 200 nM. The compounds of Examples 45, 52, and 80 provided a relative IC 50 of greater than 200 nM.

Claims

1. A compound of the formula: wherein R is H or R1 is H, halogen, CN, C1-C3 alkyl, C3-C6 cycloalkyl, C1-C3 alkoxy, C2-C3 alkenyl, OCF3, R2 is H, halogen, C1-C3 alkyl, C1-C3 alkoxy, or C2-C3 alkenyl; R3 is NH2, or CH2NH2; and X is O, OCH2, OCH2CH2, CH2O, SCH2, CH2S, CH2, NHCH2, CH2NH, N(CH3)CH2, CH2CH2, C≡C, or a bond, wherein X is connected to phenyl ring A at the ortho or the meta position, or a pharmaceutically acceptable salt thereof, and wherein the compound is not: or 2. The compound according to claim 1 wherein R3 is NH2, or a pharmaceutically acceptable salt thereof.

3. The compound according to either claim 1 or claim 2 wherein R is (a) H, or a pharmaceutically acceptable salt thereof; or (b) or a pharmaceutically acceptable salt thereof.

4. The compound according to any one of claims 1-3 wherein R1 is: (a) C1-C3 alkyl, or a pharmaceutically acceptable salt thereof; (b) CH3, or a pharmaceutically acceptable salt thereof; (c) C1-C3 alkoxy, or a pharmaceutically acceptable salt thereof; (d) OCH3, or a pharmaceutically acceptable salt thereof; or (e) F, or a pharmaceutically acceptable salt thereof.

5. The compound according to any one of claims 1-4 wherein R2 is F, or a pharmaceutically acceptable salt thereof.

6. The compound according to any one of claims 1-5 wherein X is: (a) OCH2, or a pharmaceutically acceptable salt thereof; (b) O, or a pharmaceutically acceptable salt thereof; (c) CH2, or a pharmaceutically acceptable salt thereof; (d) SCH2, or a pharmaceutically acceptable salt thereof; or (e) a bond, or a pharmaceutically acceptable salt thereof.

7. The compound according to claim 1 wherein the compound is of the formula: or a pharmaceutically acceptable salt thereof.

8. The compound according to claim 1 wherein the compound is of the formula: or a pharmaceutically acceptable salt thereof.

9. The compound according to claim 8 wherein the compound is: or a pharmaceutically acceptable salt thereof, optionally which is:

10. The compound according to claim 1 wherein the compound is: or a pharmaceutically acceptable salt thereof, optionally which is:

11. The compound according to claim 7 wherein the compound is: or a pharmaceutically acceptable salt thereof, optionally which is:

12. The compound according to claim 1 wherein the compound is: or a pharmaceutically acceptable salt thereof, optionally which is:

13. The compound according to claim 1 wherein the compound is: or a pharmaceutically acceptable salt thereof, optionally which is:

14. The compound according to claim 1 wherein the compound is: or a pharmaceutically acceptable salt thereof, optionally which is:

15. The compound according to claim 1 selected from: 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60 61 62 63 64 65 66 67 68 69 70 71 72 73 74 75 76 77 78 79 80 81 82 83 84 85 86 87 88 89 90 91 92 93 94 95 96 97 98 99 100 101 102 103 104 105 106 107 108 109 110 111 112 113 114 115 116 117 118 119 120 121 122 123 124 125 126 127 128 129 130 131 132 133 134 135 136 137 138 139 140 141 142 143 144 145 146 147 148 149 150 151 152 153 154 155 156 157 158 and159 and pharmaceutically acceptable salts thereof.

16. A compound or pharmaceutically acceptable salt thereof according to any one of claims 1 to 15 for use in therapy.

17. A compound or pharmaceutically acceptable salt thereof according to any one of claims 1 to 15 for use in the treatment of: (a) atopic dermatitis; or (b) rheumatoid arthritis.

18. A pharmaceutical composition, comprising a compound or a pharmaceutically acceptable salt thereof, according to any one of claims 1 to 15 with one or more pharmaceutically acceptable carriers, diluents, or excipients.

19. A process for preparing a pharmaceutical composition, comprising admixing a compound or a pharmaceutically acceptable salt thereof according to any one of claims 1 to 15 with one or more pharmaceutically acceptable carriers, diluents, or excipients.