Anticholinergic drugs

Abstract

Compounds of formula (I), pharmaceutical compositions and methods of use related to muscarinic acetylcholine receptors. The compounds of the present application are generally muscarinic acetylcholine receptor antagonists, such as M3 antagonists, which can be used to treat a variety of disorders, conditions or diseases, such as hyperhidrosis.

Description

[0001] In various embodiments, the present application relates to novel compounds, pharmaceutical compositions, methods of making and methods of using the same, for example, to provide anticholinergic effects. Background Art

[0002] Muscarinic acetylcholine receptors, or mAChRs, are acetylcholine receptors that form G protein-coupled receptor complexes in cell membranes. Five subtypes of muscarinic receptors have been identified, named M1-M5. M1, M3, and M5 receptors are G q protein, while M2 and M4 receptors are coupled to G i / o protein coupling. mAChRs are widely expressed in different tissues and cells and regulate many important functions of the central and peripheral nervous systems. In the bladder, M2 and M3 receptors are mainly expressed in the detrusor muscle of various species. Both M1 and M3 receptors are expressed in salivary glands, sweat glands, apocrine glands, sublingual glands and lacrimal glands, while M3 receptors are mainly expressed in the parotid gland. In the gastrointestinal tract, both M2 and M3 are expressed in smooth muscle, and M3 receptors are believed to play an important role in choline stimulation of gastrointestinal motility. In the brain, M3 receptors are less expressed, while M1, M2, M4 and M5 receptors are expressed in large quantities in different regions. M1 and M4 receptors are expressed in the human eye. M2 and M3 receptors are expressed in the human heart and regulate heart rate and heart function. Muscarinic anticholinergics have been used to treat a variety of different diseases or disorders, such as diarrhea, allergies, asthma, atrial fibrillation with bradycardia, motion sickness, anxiety, hyperhidrosis, low heart rate, overactive bladder, breathing problems such as asthma and chronic obstructive pulmonary disease, and neurological problems such as Parkinson's disease and Alzheimer's disease.

[0003] Various muscarinic acetylcholine receptor antagonists have been reported, such as the natural atropine and scopolamine as well as a number of synthetic agents, such as homatropine and eucatropine, etc. However, there is still a need for new muscarinic antagonists for various indications. Summary of the invention

[0004] In various embodiments, the present application is based, in part, on novel compounds / salts that can provide anticholinergic effects, in particular, as muscarinic acetylcholine receptor antagonists.

[0005] Some embodiments of the present application relate to salts of formula I:

[0006]

[0007] The variable R 1 , R 2 , R 3 , R 4 , L 1 , X -and j are defined in the present application. In some embodiments, the present application provides a sub-formula of Formula I, such as a salt of Formula I-1, I-1-E1, I-1-E2, I-1-E3, I-1-E4, I-2, I-2-E1, I-2-E2, I-2-E3, I-2-E4, I-3, I-3-E1, I-3-E2, I-3-E3, I-3-E4, I-4, I-4-E1, I-4-E2, I-4-E3, I-4-E4, I-5 or I-6 as described in the present application. The salt of Formula I in the present application is generally a muscarinic receptor antagonist. The salt of Formula I can be prepared from the corresponding compound of Formula II:

[0008]

[0009] The variable R 1 , R 2 , R 3 , L 1 and j are defined in the present application. In some embodiments, the present application also provides pharmaceutically acceptable salts of compounds of Formula II (eg, Formula II-1 or II-2).

[0010] Certain embodiments of the present application relate to a pharmaceutical composition comprising one or more compounds / salts described herein (e.g., compounds / salts shown in Formula I (e.g., Formula I-1, I-1-E1, I-1-E2, I-1-E3, I-1-E4, I-2, I-2-E1, I-2-E2, I-2-E3, I-2-E4, I-3, I-3-E1, I-3-E2, I-3-E3, I-3-E4, I-4, I-4-E1, I-4-E2, I-4-E3, I-4-E4, I-5 or I-6), any one of Examples 1-12, or any salt shown in Table 1 or Table 2 of the present application, or a pharmaceutically acceptable salt thereof) and optional pharmaceutically acceptable excipients. The pharmaceutical composition described herein can be formulated for different routes of administration, such as oral administration, parenteral administration, topical administration, inhalation, eye drops, etc. For example, in some embodiments, the pharmaceutical composition can be formulated for topical administration, such as in the form of a topical solution, cream, ointment, mousse, gel, toner, or powder.

[0011] Some embodiments of the present application relate to a method of treating or preventing a possible

[0012] In some embodiments, the method comprises administering to a subject an effective amount of a compound of the present application (e.g., Formula I (e.g., Formula I-1, I-1-E1, I-1-E2, I-1-E3, I-1-E4, I-2, I-2-E1, I-2-E2, I-2-E3, I-2-E4, I-3, I-3-E1, I-3-E2, I-3-E3, I-3-E4, I-4, I-4-E1, I-4-E2, I-4-E3, I-4-E4,

[0013] I-5 or I-6), any one of Examples 1-12, or any salt shown in Table 1 or Table 2 of the present application, or a pharmaceutically acceptable salt thereof) or an effective amount of the pharmaceutical composition described in the present application.

[0014] Some embodiments of the present application relate to a method for inhibiting mAChRs in a subject or biological sample, such as

[0015] In some embodiments, the method comprises treating mAChRs, such as M3 receptors, with an effective amount of a compound of the present application (e.g., Formula I (e.g., Formula I-1, I-1-E1, I-1-E2, I-1-E3,

[0016] I-1-E4, I-2, I-2-E1, I-2-E2, I-2-E3, I-2-E4, I-3, I-3-E1, I-3-E2, I-3-E3, I-3-E4,

[0017] I-4, I-4-E1, I-4-E2, I-4-E3, I-4-E4, I-5 or I-6), any one of Examples 1-12, or any salt shown in Table 1 or Table 2 of the present application, or a pharmaceutically acceptable salt thereof) or an effective amount of the pharmaceutical composition described herein.

[0018] In some specific embodiments, the present application provides a method for treating hyperhidrosis in a subject in need thereof. In some embodiments, the method comprises administering to the subject a therapeutically effective amount of a compound of the present application (e.g., Formula I (e.g., I-1, I-1-E1, I-1-E2, I-1-E3, I-1-E4, I-2, I-2-E1, I-2-E2,

[0019] I-2-E3, I-2-E4, I-3, I-3-E1, I-3-E2, I-3-E3, I-3-E4, I-4, I-4-E1, I-4-E2, I-4-E3,

[0020] I-4-E4, I-5 or I-6), any of Examples 1-12, or any salt shown in Table 1 or Table 2 of the present application, or a pharmaceutically acceptable salt thereof) or an effective amount of a pharmaceutical composition described herein. Typically, administration is by topical route. In some embodiments, one or more compounds / salts of the present application may be administered as the sole active ingredient. In some embodiments, one or more compounds of the present application may be used in combination with an additional therapy, for example, an additional therapy that is effective in treating hyperhidrosis.

[0021] It should be understood that the foregoing summary of the invention and the following detailed description are only exemplary and explanatory.

[0022] The present invention is not limited thereto. DETAILED DESCRIPTION

[0023] The present application generally relates to compounds useful as muscarinic anticholinergics. The compounds of the present application are generally useful for treating or preventing various diseases or disorders mediated by such muscarinic cholinergic receptors as described herein, such as those mediated by M3 receptors.

[0024] Compound

[0025] Formula I

[0026] In some embodiments, the present application provides a salt represented by general formula I:

[0027]

[0028] in:

[0029] X - is the counter ion;

[0030] R 1 is hydrogen or optionally substituted C 3-8 Carbocyclic group;

[0031] L 1 Empty, C 1-4 Alkylene, or C 1-4 heteroalkylene;

[0032] R 2 For hydrogen, C 1-6 Alkyl, C 2-6 Alkenyl, C 2-6 Alkynyl, C 3-8 carbocyclyl, 4-8 membered heterocyclyl, phenyl, or 5-10 membered heteroaryl, each of which is optionally substituted;

[0033] R 3 and R 4 are independently hydrogen or C 1-6Alkyl; and

[0034] j is 0, 1 or 2.

[0035] In some embodiments, the salt shown in Formula I (including any applicable sub-formula as described herein) may contain one or more asymmetric centers and / or axial chirality, and therefore may exist in various stereoisomeric forms, for example, enantiomers and / or diastereomers. In some embodiments, the salt shown in Formula I may exist in the form of a single enantiomer and / or diastereomer (if applicable) or a mixture of stereoisomers (including racemic mixtures and enriched in one or stereoisomers). In some embodiments, as applicable, the salt shown in Formula I (including any applicable sub-formula as described herein) may exist as a single enantiomer substantially free of (e.g., less than 20%, less than 10%, less than 5%, less than 1%, or with an undetectable amount by weight, by HPLC area, or both) of the separation of another enantiomer. In some embodiments, as applicable, the salts shown in Formula I (including any applicable sub-formulas as described herein) can be present as isolated single diastereomers that are substantially free (e.g., less than 20%, less than 10%, less than 5%, less than 1%, or with undetectable amounts by weight, by HPLC area, or both) of another diastereomer. In some embodiments, as applicable, the salts shown in Formula I (including any applicable sub-formulas as described herein) can also be present as mixtures of stereoisomers in any ratio, such as racemic mixtures.

[0036] In some embodiments, the salt of Formula I may have the general formula I-1;

[0037]

[0038] Wherein the variables include any of those variables in any combination described in this application.

[0039] In some embodiments, the salt represented by Formula I-1 may have Formula I-1-E1 or Formula I-1-E2:

[0040]

[0041] In some embodiments, the salt represented by Formula I-1 may have Formula I-1-E3 or Formula I-1-E4:

[0042]

[0043] In some embodiments, the salt shown in the general formula I-1 can be a substantially pure stereoisomer with the general formula I-1-E1, which can be substantially free of any corresponding isomeric forms of the general formula I-1-E2, the general formula I-1-E3, and the general formula I-1-E4. For example, in some embodiments, among the four possible stereoisomers, the combined amount of the general formula I-1-E2, the general formula I-1-E3, and the general formula I-1-E4 that may be present is less than 20%, less than 10%, less than 5%, less than 1% by weight, by HPLC area, or both, or the general formula I-1-E2, the general formula I-1-E3, and the general formula I-1-E4 are all undetectable. In some embodiments, the salt shown in the general formula I-1 can be a substantially pure stereoisomer with the general formula I-1-E2, which can be substantially free of any corresponding isomeric forms of the general formula I-1-E1, the general formula I-1-E3, and the general formula I-1-E4. For example, in some embodiments, among the four possible stereoisomers, the combined amount of Formula I-1-E1, Formula I-1-E3 and Formula I-1-E4 that may be present is less than 20%, less than 10%, less than 5%, less than 1% by weight, by HPLC area, or both, or Formula I-1-E1, Formula I-1-E3 and Formula I-1-E4 are all undetectable. In some embodiments, the salt shown in Formula I-1 can be a substantially pure stereoisomer having Formula I-1-E3, which can be substantially free of any corresponding isomeric forms of Formula I-1-E1, Formula I-1-E2 and Formula I-1-E4. For example, in some embodiments, among the four possible stereoisomers, the combined amount of Formula I-1-E1, Formula I-1-E2 and Formula I-1-E4 that may be present is less than 20%, less than 10%, less than 5%, less than 1% by weight, by HPLC area, or both, or Formula I-1-E1, Formula I-1-E2 and Formula I-1-E4 are all undetectable. In some embodiments, the salt shown in Formula I-1 can be a substantially pure stereoisomer having Formula I-1-E4, which can be substantially free of any corresponding isomeric forms of Formula I-1-E1, Formula I-1-E2 and Formula I-1-E3.

[0044] For example, in some embodiments, among the four possible stereoisomers, the combined amount of the possible existence of general formula I-1-E1, general formula I-1-E2 and general formula I-1-E3 is less than 20%, less than 10%, less than 5%, less than 1% by weight, by HPLC area, or both, or general formula I-1-E1, general formula I-1-E2 and general formula I-1-E3 are all undetectable. In some embodiments, a salt represented by a given general formula I-1 may exist in the form of a mixture of any two or more of the four possible stereoisomers general formulas I-1-E1, I-1-E2, I-1-E3 and I-1-E4 in any proportion.

[0045] In some embodiments, the compound of formula I may have the formula I-2:

[0046]

[0047] Wherein the variables include any of those variables in any combination described in this application.

[0048] In some embodiments, the salt represented by the general formula I-2 may have the general formula I-2-E1 or the general formula I-2-E2:

[0049]

[0050] In some embodiments, the salt represented by the general formula I-2 may have the general formula I-2-E3 or the general formula I-2-E4:

[0051]

[0052] In some embodiments, the salt shown in the general formula I-2 can be a substantially pure stereoisomer with the general formula I-2-E1, which can be substantially free of any corresponding isomeric forms of the general formula I-2-E2, the general formula I-2-E3, and the general formula I-2-E4. For example, in some embodiments, among the four possible stereoisomers, the combined amount of the general formula I-2-E2, the general formula I-2-E3, and the general formula I-2-E4 that may be present is less than 20%, less than 10%, less than 5%, less than 1% by weight, by HPLC area, or both, or the general formula I-2-E2, the general formula I-2-E3, and the general formula I-2-E4 are all undetectable. In some embodiments, the salt shown in the general formula I-2 can be a substantially pure stereoisomer with the general formula I-2-E2, which can be substantially free of any corresponding isomeric forms of the general formula I-2-E1, the general formula I-2-E3, and the general formula I-2-E4. For example, in some embodiments, among the four possible stereoisomers, the combined amount of Formula I-2-E1, Formula I-2-E3 and Formula I-2-E4 that may be present is less than 20%, less than 10%, less than 5%, less than 1% by weight, by HPLC area, or both, or Formula I-2-E1, Formula I-2-E3 and Formula I-2-E4 are all undetectable. In some embodiments, the salt shown in Formula I-2 can be a substantially pure stereoisomer having Formula I-2-E3, which can be substantially free of any corresponding isomeric forms of Formula I-2-E1, Formula I-2-E2 and Formula I-2-E4. For example, in some embodiments, among the four possible stereoisomers, the combined amount of Formula I-2-E1, Formula I-2-E2 and Formula I-2-E4 that may be present is less than 20%, less than 10%, less than 5%, less than 1% by weight, by HPLC area, or both, or Formula I-2-E1, Formula I-2-E2 and Formula I-2-E4 are all undetectable. In some embodiments, the salt shown in Formula I-2 can be a substantially pure stereoisomer having Formula I-2-E4, which can be substantially free of any corresponding isomeric forms of Formula I-2-E1, Formula I-2-E2 and Formula I-2-E3.

[0053] For example, in some embodiments, among the four possible stereoisomers, the combined amount of the possible existence of general formula I-2-E1, general formula I-2-E2 and general formula I-2-E3 is less than 20%, less than 10%, less than 5%, less than 1% by weight, by HPLC area, or both, or general formula I-2-E1, general formula I-2-E2 and general formula I-2-E3 are all undetectable. In some embodiments, the salt shown in general formula I-2 can exist in the form of a mixture of any two or more of the four possible stereoisomers general formula I-2-E1, I-2-E2, I-2-E3 and I-2-E4 in any proportion.

[0054] Typically, j in Formula I (e.g., Formula I-1, I-1-E1, I-1-E2, I-1-E3, I-1-E4, I-2, I-2-E1, I-2-E2, I-2-E3, I-2-E4) is 0, 1 or 2. Preferably, j in Formula I (e.g., Formula I-1, I-1-E1, I-1-E2, I-1-E3, I-1-E4, I-2, I-2-E1, I-2-E2, I-2-E3, I-2-E4) is 1.

[0055] For example, in some embodiments, Formula I can be characterized as having Formula I-3 or Formula I-4:

[0056]

[0057] In some embodiments, the salt of formula I-3 may have the formula I-3-E1 or the formula I-13-E2:

[0058]

[0059] In some embodiments, the salt of formula I-3 may have the formula I-3-E3 or the formula I-3-E4:

[0060]

[0061] In some embodiments, the salt shown in the general formula I-3 can be a substantially pure stereoisomer with the general formula I-3-E1, which can be substantially free of any corresponding isomeric forms of the general formula I-3-E2, the general formula I-3-E3, and the general formula I-3-E4. For example, in some embodiments, among the four possible stereoisomers, the combined amount of the general formula I-3-E2, the general formula I-3-E3, and the general formula I-3-E4 that may be present is less than 20% by weight, less than 10% by HPLC area, or less than 5%, less than 1%, or the general formula I-3-E2, the general formula I-3-E3, and the general formula I-3-E4 are all undetectable. In some embodiments, the salt shown in the general formula I-3 can be a substantially pure stereoisomer with the general formula I-3-E2, which can be substantially free of any corresponding isomeric forms of the general formula I-3-E1, the general formula I-3-E3, and the general formula I-3-E4. For example, in some embodiments, among the four possible stereoisomers, the combined amount of Formula I-3-E1, Formula I-3-E3 and Formula I-3-E4 that may be present is less than 20%, less than 10%, less than 5%, less than 1% by weight, by HPLC area, or both, or Formula I-3-E1, Formula I-3-E3 and Formula I-3-E4 are all undetectable. In some embodiments, the salt shown in Formula I-3 can be a substantially pure stereoisomer having Formula I-3-E3, which can be substantially free of any corresponding isomeric forms of Formula I-3-E1, Formula I-3-E2 and Formula I-3-E4. For example, in some embodiments, among the four possible stereoisomers, the combined amount of Formula I-3-E1, Formula I-3-E2 and Formula I-3-E4 that may be present is less than 20%, less than 10%, less than 5%, less than 1% by weight, by HPLC area, or both, or Formula I-3-E1, Formula I-3-E2 and Formula I-3-E4 are all undetectable. In some embodiments, the salt shown in Formula I-3 can be a substantially pure stereoisomer having Formula I-3-E4, which can be substantially free of any corresponding isomeric forms of Formula I-3-E1, Formula I-3-E2 and Formula I-3-E3.

[0062] For example, in some embodiments, among the four possible stereoisomers, the combined amount of the possible existence of general formula I-3-E1, general formula I-3-E2 and general formula I-3-E3 is less than 20%, less than 10%, less than 5%, less than 1% by weight, by HPLC area, or both, or general formula I-3-E1, general formula I-3-E2 and general formula I-3-E3 are all undetectable. In some embodiments, the salt shown in general formula I-3 can exist in the form of a mixture of any two or more of the four possible stereoisomers general formula I-3-E1, I-3-E2, I-3-E3 and I-3-E4 in any proportion.

[0063] In some embodiments, the salt of formula I-4 may have the formula I-4-E1 or the formula I-4-E2:

[0064]

[0065] In some embodiments, the salt of formula I-4 may have the formula I-4-E3 or the formula I-4-E4:

[0066]

[0067] In some embodiments, the salt shown in the general formula I-4 can be a substantially pure stereoisomer with the general formula I-4-E1, which can be substantially free of any corresponding isomeric forms of the general formula I-4-E2, the general formula I-4-E3, and the general formula I-4-E4. For example, in some embodiments, among the four possible stereoisomers, the combined amount of the general formula I-4-E2, the general formula I-4-E3, and the general formula I-4-E4 that may be present is less than 20%, less than 10%, less than 5%, less than 1% by weight, by HPLC area, or both, or the general formula I-4-E2, the general formula I-4-E3, and the general formula I-4-E4 are all undetectable. In some embodiments, the salt shown in the general formula I-4 can be a substantially pure stereoisomer with the general formula I-4-E2, which can be substantially free of any corresponding isomeric forms of the general formula I-4-E1, the general formula I-4-E3, and the general formula I-4-E4. For example, in some embodiments, among the four possible stereoisomers, the combined amount of Formula I-4-E1, Formula I-4-E3 and Formula I-4-E4 that may be present is less than 20%, less than 10%, less than 5%, less than 1% by weight, by HPLC area, or both, or Formula I-4-E1, Formula I-4-E3 and Formula I-4-E4 are all undetectable. In some embodiments, the salt shown in Formula I-4 can be a substantially pure stereoisomer having Formula I-4-E3, which can be substantially free of any corresponding isomeric forms of Formula I-4-E1, Formula I-4-E2 and Formula I-4-E4. For example, in some embodiments, among the four possible stereoisomers, the combined amount of Formula I-4-E1, Formula I-4-E2 and Formula I-4-E4 that may be present is less than 20%, less than 10%, less than 5%, less than 1% by weight, by HPLC area, or both, or Formula I-4-E1, Formula I-4-E2 and Formula I-4-E4 are all undetectable. In some embodiments, the salt shown in Formula I-4 can be a substantially pure stereoisomer having Formula I-4-E4, which can be substantially free of any corresponding isomeric forms of Formula I-4-E1, Formula I-4-E2 and Formula I-4-E3.

[0068] For example, in some embodiments, among the four possible stereoisomers, the combined amount of the possible existence of general formula I-4-E1, general formula I-4-E2 and general formula I-4-E3 is less than 20%, less than 10%, less than 5%, less than 1% by weight, by HPLC area, or both, or general formula I-4-E1, general formula I-4-E2 and general formula I-4-E3 are all undetectable. In some embodiments, the salt shown in general formula I-4 can exist in the form of a mixture of any two or more of the four possible stereoisomers general formula I-4-E1, I-4-E2, I-4-E3 and I-4-E4 in any proportion.

[0069] In some embodiments, Formula I (e.g., Formula I-1, I-1-E1, I-1-E2, I-1-E3, I-1-E4, I-2, I-2-E1, I-2-E2, I-2-E3, I-2-E4, I-3, I-3-E1, I-3-E2, I-3-E3, I-3-E4, I-4,

[0070] I-4-E1, I-4-E2, I-4-E3, I-4-E4, L in) 1 It can be empty, in which case the C(O)-O group in Formula I is directly connected to the nitrogen-containing ring of Formula I.

[0071] In some embodiments, Formula I (e.g., Formula I-1, I-1-E1, I-1-E2, I-1-E3, I-1-E4, I-2, I-2-E1, I-2-E2, I-2-E3, I-2-E4, I-3, I-3-E1, I-3-E2, I-3-E3, I-3-E4, I-4,

[0072] L in I-4-E1, I-4-E2, I-4-E3, I-4-E4) 1 Can be C 1-4 Alkylene, such as CH2.

[0073] In some preferred embodiments, L in Formula I-1, I-1-E1, I-1-E2, I-1-E3, I-1-E4, I-3, I-3-E1, I-3-E2, I-3-E3 or I-3-E4 1 is CH2. For example, in some embodiments, the salts represented by Formula I-1, I-1-E1, I-1-E2, I-1-E3, I-1-E4, I-3, I-3-E1, I-3-E2, I-3-E3, or I-3-E4 can be characterized as having Formula I-5:

[0074]

[0075] In some preferred embodiments, L in Formula I-2, I-2-E1, I-2-E2, I-2-E3, I-2-E4, I-4, I-4-E1, I-4-E2, I-4-E3 or I-4-E4 1 Empty, R 1 For example, in some embodiments, the salts represented by the general formula I-2, I-2-E1, I-2-E2, I-2-E3, I-2-E4, I-4, I-4-E1, I-4-E2, I-4-E3 or I-4-E4 can be characterized as having the general formula I-6:

[0076]

[0077] Typically, general formula I (for example, general formula I-1, I-1-E1, I-1-E2, I-1-E3, I-1-E4, I-2, I-2-E1, I-2-E2, I-2-E3, I-2- R in E4, I-3, I-3-E1, I-3-E2, I-3-E3, I-3-E4, I-4, I-4-E1, I-4-E2, I-4-E3, I-4-E4, I-5) 1 It's hydrogen.

[0078] In some embodiments, Formula I (e.g., Formula I-1, I-1-E1, I-1-E2, I-1-E3, I-1-E4, I-2, I-2-E1, I-2-E2, I-2-E3, I-2-E4, I-3, I-3-E1, I-3-E2, I-3-E3, I-3-E4, I-4,

[0079] R in I-4-E1, I-4-E2, I-4-E3, I-4-E4, I-5) 1 It may also be an optionally substituted C 3-8 Carbocyclic groups, for example cyclopentyl.

[0080] Various groups are suitable as R of the general formula I 2 Generally, R in Formula I 2 Not hydrogen. However,

[0081] In some embodiments, Formula I (e.g., Formula I-1, I-1-E1, I-1-E2, I-1-E3, I-1-E4, I-2, I-2-E1, I-2-E2, I-2-E3, I-2 -R in E4, I-3, I-3-E1, I-3-E2, I-3-E3, I-3-E4, I-4, I-4-E1, I-4-E2, I-4-E3, I-4-E4, I-5, I-6) 2 It can also be hydrogen. 2When it is hydrogen,

[0082] R 1 Usually not hydrogen.

[0083] In some embodiments, Formula I (e.g., Formula I-1, I-1-E1, I-1-E2, I-1-E3, I-1-E4, I-2, I-2-E1, I-2-E2, I-2-E3, I-2-E4, I-3, I-3-E1, I-3-E2, I-3-E3, I-3-E4, I-4,

[0084] R in I-4-E1, I-4-E2, I-4-E3, I-4-E4, I-5, I-6) 2 It may be an optionally substituted C 1-6 For example, in some embodiments, R 2 Can be C 1-6 alkyl, which is optionally substituted by one or more (e.g., 1, 2 or 3) independently selected from F, OH, R A , OR A and phenyl, wherein the phenyl is optionally substituted by one or more (e.g., 1, 2 or 3) independently selected from halogen (e.g., F or Cl), OH, C 1-4 Alkyl, fluorine-substituted C 1-4 Alkyl, C 1-4 Alkoxy and fluorine substituted C 1-4 The alkoxy substituents are substituted, wherein R A Each occurrence is independently C 1-4 Alkyl or C 3-6 Cycloalkyl, which is optionally substituted by one or more (e.g., 1, 2 or 3) independently selected from F, OH, C 1-4 Alkyl, fluorine-substituted C 1-4 Alkyl, C 1-4 Alkoxy and fluorine substituted C 1-4 In some embodiments, R 2 Can be C 3-6 Alkyl groups, such as branched C 3-6 Alkyl, for example isopropyl.

[0085] In some embodiments, Formula I (e.g., Formula I-1, I-1-E1, I-1-E2, I-1-E3, I-1-E4, I-2, I-2-E1, I-2-E2, I-2-E3, I-2-E4, I-3, I-3-E1, I-3-E2, I-3-E3, I-3-E4, I-4,

[0086] R in I-4-E1, I-4-E2, I-4-E3, I-4-E4, I-5, I-6)2 It may be an optionally substituted C 3-8 Carbocyclic group.

[0087] In some preferred embodiments, Formula I (e.g., Formula I-1, I-1-E1, I-1-E2, I-1-E3, I-1-E4, I-2, I-2-E1, I-2-E2, I-2-E3, I- 2-E4, I-3, I-3-E1, I-3-E2, I-3-E3, I-3-E4, I-4, I-4-E1, I-4-E2, I-4-E3, I-4-E4, I-5, I-6) in R 2 It may be an optionally substituted C 3-6 Cycloalkyl, for example cyclopropyl, cyclobutyl, cyclopentyl or cyclohexyl. For example, in some embodiments, R 2 Can be C 3-6 Cycloalkyl, which is optionally substituted by one or more (e.g., 1, 2 or 3) independently selected from F, OH, R A OR A Substituents, where R A Each occurrence is independently C 1-4 Alkyl or C 3-6 Cycloalkyl, which is optionally substituted by one or more (e.g., 1, 2 or 3) independently selected from F, OH, C 1-4 Alkyl, fluorine-substituted C 1-4 Alkyl, C 1-4 Alkoxy and fluorine substituted C 1-4 In some embodiments, R in Formula I (e.g., Formula I-1, I-1-E1, I-1-E2, I-1-E3, I-1-E4, I-2, I-2-E1, I-2-E2, I-2-E3, I-2-E4, I-3, I-3-E1, I-3-E2, I-3-E3, I-3-E4, I-4, I-4-E1, I-4-E2, I-4-E3, I-4-E4, I-5, I-6) 2 It may be cyclopropyl, cyclobutyl, cyclopentyl or cyclohexyl, more preferably cyclopentyl.

[0088] In some preferred embodiments, Formula I (e.g., Formula I-1, I-1-E1, I-1-E2, I-1-E3, I-1-E4, I-2, I-2-E1, I-2-E2, I-2-E3, I- R in 2-E4, I-3, I-3-E1, I-3-E2, I-3-E3, I-3-E4, I-4, I-4-E1, I-4-E2, I-4-E3, I-4-E4, I-5, I-6) 2 It may be an optionally substituted C 4-7Cycloalkenyl, for example, has one carbon-carbon double bond in the ring. For example, in some embodiments, R 2 Can be C 4-7 Cycloalkenyl, optionally substituted by one or more (e.g., 1, 2 or 3) independently selected from F, OH, R A OR A Substituents, where R A Each occurrence is independently C 1-4 Alkyl or C 3-6 Cycloalkyl, which is optionally substituted by one or more (e.g., 1, 2 or 3) independently selected from F, OH, C 1-4 Alkyl, fluorine-substituted C 1-4 Alkyl, C 1-4 Alkoxy and fluorine substituted C 1-4 In some embodiments, the general formula I (e.g., general formula I-1, I-1-E1, I-1-E2, I-1-E3, I-1-E4, I-2, I-2-E1, I-2-E2, I-2-E3, I-2-E4, I-3, I-3-E1, I-3-E2, I-3-E3, I-3-E4, I-4, I-4-E1, I-4-E2, I-4-E3, I-4-E4, I-5,

[0089] R in I-6) 2 It may be a cyclopentenyl group, preferably

[0090] In some embodiments, Formula I (e.g., Formula I-1, I-1-E1, I-1-E2, I-1-E3, I-1-E4, I-2, I-2-E1, I-2-E2, I-2-E3, I-2-E4, I-3, I-3-E1, I-3-E2, I-3-E3, I-3-E4, I-4,

[0091] R in I-4-E1, I-4-E2, I-4-E3, I-4-E4, I-5, I-6) 2 It can be an optionally substituted phenyl. For example, in some embodiments, R 2 It may be phenyl, which is optionally substituted by one or more (e.g., 1, 2 or 3) independently selected from F, Cl, OH, C 1-4 Alkyl, fluorine-substituted C 1-4 Alkyl, C 1-4 Alkoxy and fluorine substituted C 1-4In some embodiments, R in Formula I (e.g., Formula I-1, I-1-E1, I-1-E2, I-1-E3, I-1-E4, I-2, I-2-E1, I-2-E2, I-2-E3, I-2-E4, I-3, I-3-E1, I-3-E2, I-3-E3, I-3-E4, I-4, I-4-E1, I-4-E2, I-4-E3, I-4-E4, I-5, I-6) is substituted with a substituent of the alkoxy group. 2 It may be phenyl.

[0092] In some embodiments, Formula I (e.g., Formula I-1, I-1-E1, I-1-E2, I-1-E3, I-1-E4, I-2, I-2-E1, I-2-E2, I-2-E3, I-2-E4, I-3, I-3-E1, I-3-E2, I-3-E3, I-3-E4, I-4,

[0093] R in I-4-E1, I-4-E2, I-4-E3, I-4-E4, I-5, I-6) 2 It may be an optionally substituted 5- or 6-membered heteroaryl having ring heteroatoms independently selected from N, O and S, for example, those described herein. 2 It may be an optionally substituted 5-membered heteroaryl having 1-3 ring heteroatoms independently selected from N, O and S, such as oxazolyl, thiazolyl, etc. In some embodiments, the 5-membered heteroaryl may be optionally substituted by one or more (e.g., 1, 2 or 3) independently selected from F, Cl, OH, C 1-4 Alkyl, fluorine-substituted C 1-4 Alkyl, C 1-4 Alkoxy and fluorine substituted C 1-4 The substituents of the alkoxy group are substituted.

[0094] In some embodiments, Formula I (e.g., Formula I-1, I-1-E1, I-1-E2, I-1-E3, I-1-E4, I-2, I-2-E1, I-2-E2, I-2-E3, I-2 -R in E4, I-3, I-3-E1, I-3-E2, I-3-E3, I-3-E4, I-4, I-4-E1, I-4-E2, I-4-E3, I-4-E4, I-5, I-6) 2 It may be an oxazolyl group, for example,

[0095] In some embodiments, Formula I (e.g., Formula I-1, I-1-E1, I-1-E2, I-1-E3, I-1-E4, I-2, I-2-E1, I-2-E2, I-2-E3, I-2-E4, I-3, I-3-E1, I-3-E2, I-3-E3, I-3-E4, I-4,

[0096] R in I-4-E1, I-4-E2, I-4-E3, I-4-E4, I-5, I-6) 2 It may be an optionally substituted 6-membered heteroaryl having 1-2 heteroatoms independently selected from N, O and S, for example, as disclosed herein, such as pyridyl or pyrimidinyl, etc. In some embodiments, the 6-membered heteroaryl may be optionally substituted by one or more (e.g., 1, 2 or 3) independently selected from F, Cl, OH, C 1-4 Alkyl, fluorine-substituted C 1-4 Alkyl, C 1-4 Alkoxy and fluorine substituted C 1-4 The substituents of the alkoxy group are substituted.

[0097] Typically, general formula I (for example, general formula I-1, I-1-E1, I-1-E2, I-1-E3, I-1-E4, I-2, I-2-E1, I-2-E2, I-2-E3, I-2-E 4. R of I-3, I-3-E1, I-3-E2, I-3-E3, I-3-E4, I-4, I-4-E1, I-4-E2, I-4-E3, I-4-E4, I-5, I-6) 3 It is C 1-6 An alkyl group is more preferably a methyl group.

[0098] Typically, general formula I (for example, general formula I-1, I-1-E1, I-1-E2, I-1-E3, I-1-E4, I-2, I-2-E1, I-2-E2, I-2-E3, I-2-E 4. R of I-3, I-3-E1, I-3-E2, I-3-E3, I-3-E4, I-4, I-4-E1, I-4-E2, I-4-E3, I-4-E4, I-5, I-6) 4 It is C 1-6 An alkyl group is more preferably a methyl group.

[0099] For the counterion X in the general formula I - There is no particular limitation, since the anticholinergic activity of the salts of Formula I is independent of X -itself. Generally, general formula I (for example, general formula I-1, I-1-E1, I-1-E2, I-1-E3, I-1-E4, I-2, I-2-E1, I-2-E2, I-2-E3, I-2-E4, I-3, I-3-E1, I-3-E2, I-3-E3, I-3-E4, I-4,

[0100] X in I-4-E1, I-4-E2, I-4-E3, I-4-E4, I-5, I-6) - X is a pharmaceutically acceptable counterion, for example, a halide (e.g., F-, Cl-, Br-, or I-). Other suitable counterions include those derived from various inorganic or organic acids, such as sulfuric acid, nitric acid, phosphoric acid, acetic acid, propionic acid, glycolic acid, pyruvic acid, oxalic acid, malic acid, malonic acid, succinic acid, maleic acid, fumaric acid, tartaric acid, citric acid, benzoic acid, cinnamic acid, mandelic acid, methanesulfonic acid, ethanesulfonic acid, p-toluenesulfonic acid, salicylic acid, etc. It should be understood that in some embodiments, X - It can also be derived from a multivalent anion that is balanced with the cationic structure of Formula I so that the overall charge of X is negative 1.

[0101] In some embodiments, the present application also provides salts selected from those in Table 1 below:

[0102] Table 1. List of exemplary salts of the present application

[0103]

[0104]

[0105] Among them, X - It is a pharmaceutically acceptable counter ion.

[0106] In some embodiments, the present application also provides salts selected from those in Table 2 below:

[0107] Table 2. List of further exemplary salts of the present application

[0108]

[0109] Among them, X - It is a pharmaceutically acceptable counter ion.

[0110] In some embodiments, the compound genus described in the present application also excludes any particular known compounds or salts prior to the present application, to the extent applicable. In some embodiments, any subgenus of compound or salt species that completely fell into the compound genus described in the present application prior to the present application, to the extent applicable, may also be excluded from the genus of the present application. For example, glycopyrrolate or its precursor is excluded from the compound / salt genus associated with Formula I or II described in the present application, to the extent applicable.

[0111] Formula II

[0112] The salts of the general formula I in the present application can usually be prepared by reacting the corresponding amines of the general formula II

[0113]

[0114] With R 4 Group donors, such as R 4 -Lg 1 Reaction, where Lg 1 is a leaving group, such as a halide (e.g., I),

[0115] The variable L 1 , R 1 , R 2 , R 3 , R 4 and j may have any of the respective definitions described in this application in any combination in relation to Formula I (including subformulae thereof).

[0116] In some embodiments, the present application also provides a compound represented by general formula II or a salt thereof,

[0117]

[0118] in:

[0119] R 1 is hydrogen or optionally substituted C 3-8 Carbocyclic group;

[0120] L 1 Empty, C 1-4 Alkylene, or C 1-4 heteroalkylene;

[0121] R 2 For hydrogen, C 1-6 Alkyl, C 2-6 Alkenyl, C 2-6 Alkynyl, C 3-8 carbocyclyl, 4-8 membered heterocyclyl, phenyl, or 5-10 membered heteroaryl, each of which is optionally substituted;

[0122] R3 is hydrogen or C 1-6 Alkyl; and

[0123] j is 0, 1 or 2.

[0124] In some embodiments, the compound represented by Formula II may have Formula II-1:

[0125]

[0126] In some embodiments, the compound of Formula II may have a general formula according to Formula II-2:

[0127]

[0128] L in the general formula II (e.g., general formula II-1 or II-2) 1 , R 1 , R 2 , R 3 The definitions of and j include any of those corresponding to those of Formula I (including its subformulae) described herein. For example, in some embodiments, L in Formula II 1 In some embodiments, L in Formula II 1

[0129] Can be C 1-4 Alkylene, such as CH2. In some embodiments, R in Formula II 1 In some embodiments, R in Formula II 1 In some embodiments, R in Formula II 2 In some embodiments, R in Formula II 2 Can be C 3-6 Cycloalkyl, such as cyclopropyl, cyclobutyl, cyclopentyl or cyclohexyl, which may be optionally substituted, for example, as described herein. In some embodiments, R in Formula II 2 Can be C 4-7 Cycloalkenyl, such as cyclopentenyl, which may be optionally substituted, for example, as described herein. In some embodiments, j in Formula II is 1. In some embodiments, R in Formula II 3 is methyl. 1 , R 1 , R 2 , R 3 Other suitable groups or definitions for and j include those discussed herein in connection with Formula I (including subformulae thereof) in any combination.

[0130] In some embodiments, the compound represented by general formula II-2 can also be used to prepare pharmaceutically acceptable salts.

[0131] For example acid addition salts or quaternary ammonium salts such as those of the general formula I.

[0132] In view of the present application, compounds of Formula II can be easily prepared by those skilled in the art, which can be used to prepare the salts of Formula I discussed in the present application. Exemplary methods are also shown in the Examples section.

[0133] For example, compounds of Formula II can be prepared according to Scheme A shown below. Thus, compound A can be coupled with compound B under ester forming conditions to provide compound C, which can then be deprotected and optionally converted to R. 2 It is obvious to those skilled in the art that R 2 The group can also be introduced in the early stage of the synthesis. Therefore, in some embodiments, R 2 It can also be the same as the G group. 2 In different cases, it is usually a leaving group, such as a halogen or a sulfonate containing a leaving group (e.g., O-Ts, O-Ms, O-Tf), which can react with R 2 Donor reaction, for example under palladium-catalyzed cross-coupling conditions. Pg in compounds A and C 1 Typically, it is an oxygen protecting group such as described herein. 1 There is no particular limitation on the suitable protecting group of 1 , R 1 , R 2 , R 3 The definitions of and j include any corresponding definitions described in this application in any combination in relation to Formula II (including subformulae thereof).

[0134]

[0135] It will be apparent to those skilled in the art that conventional protecting groups may be required to prevent certain functional groups from undergoing undesired reactions. Suitable protecting groups for various functional groups and suitable conditions for protecting and deprotecting particular functional groups are well known in the art. For example, in Protective Groups in Organic Synthesis, 4 thMany protecting groups are described in ed. PGM Wuts; TW Greene, John Wiley, 2007, and references cited therein. The reagents used in the reactions described herein are generally known compounds or can be prepared by known methods or obvious modifications thereof. For example, many reagents are available from commercial suppliers, such as Aldrich Chemical Co. (Milwaukee, Wisconsin, USA), Sigma

[0136] (St. Louis, MO, USA). Other reagents can be prepared by methods described in standard reference texts, or obvious modifications thereof, such as Fieser and Fieser's Reagents for Organic Synthesis, Volumes 1-15 (John Wiley and Sons, 1991), Rodd's Chemistry of Carbon Compounds, Volumes 1-5 and Supplemental (Elsevier Science Publishers, 1989), Organic Reactions, Volumes 1-40 (John Wiley and Sons, 1991), March's Advanced Organic Chemistry, (Wiley, 7 th Edition) and Larock's Comprehensive Organic Transformations (Wiley-VCH, 1999), and any available updates as of the filing date of this application.

[0137] Pharmaceutical composition

[0138] Certain embodiments relate to pharmaceutical compositions comprising one or more compounds / salts of the present application.

[0139] The pharmaceutical composition can selectively include a pharmaceutically acceptable excipient. In some embodiments, the pharmaceutical composition includes a compound / salt of the present application (e.g., general formula I (e.g., general formula I-1, I-1-E1, I-1-E2, I-1-E3, I-1-E4, I-2, I-2-E1, I-2-E2, I-2-E3, I-2-E4, I-3, I-3-E1, I-3-E2, I-3-E3, I-3-E4, I-4, I-4-E1, I-4-E2, I-4-E3, I-4-E4, I-5 or I-6) shown in a compound / salt, any one of embodiments 1-12 or any one shown in Table 1 or Table 2 of the present application, or a pharmaceutically acceptable salt thereof) and a pharmaceutically acceptable excipient. Pharmaceutically acceptable excipients are known in the art. Suitable non-limiting excipients include, for example, encapsulating materials or additives such as antioxidants, binders, buffers, carriers, coating agents, colorants, diluents, disintegrants, emulsifiers, extenders, fillers, flavoring agents, humectants, lubricants, flavoring agents, preservatives, propellants, release agents, sterilants, sweeteners, solubilizers, wetting agents and mixtures thereof. See also Remington's The Science and Practice of Pharmacy, 21st Edition, A. R. Gennaro (Lippincott, Williams & Wilkins, Baltimore, Md., 2005; incorporated herein by reference), which discloses various excipients used in formulating pharmaceutical compositions and known preparation techniques thereof.

[0140] The pharmaceutical composition may include any one or more compounds described herein. For example, in some embodiments, the pharmaceutical composition comprises, for example, a therapeutically effective amount of Formula I (e.g., Formula I-1, I-1-E1, I-1-E2, I-1-E3, I-1-E4, I-2, I-2-E1, I-2-E2, I-2-E3, I-2-E4, I-3, I-3-E1, I-3-E2, I-3-E3, I-3-E4, I-4, I-4-E1, I-4-E2, I-4-E3, I-4-E4, I-5 or I-6), any one of Examples 1-12, or any salt shown in Table 1 or Table 2 of the present application, or a pharmaceutically acceptable salt thereof. In any embodiment described in the present application, the pharmaceutical composition may include any compound / salt selected from Examples 1-12, or any salt shown in Table 1 or Table 2 of the present application, or a pharmaceutically acceptable salt thereof.

[0141] The pharmaceutical composition in the present application can be formulated for delivery by any known delivery route, including but not limited to oral, intranasal, transdermal, pulmonary, inhalation, buccal, sublingual, intraperitoneal, subcutaneous, intramuscular, intravenous, rectal, intrathoracic, intrathecal or non-digestive way. For example, in some embodiments, the pharmaceutical composition in the present application can be formulated for local delivery. In some embodiments, the pharmaceutical composition of the present application can be formulated for oral administration. In some embodiments, the pharmaceutical composition of the present application can be formulated for non-digestive administration. In some embodiments, the pharmaceutical composition of the present application can be formulated for inhalation, such as aerosol spray, dry powder, etc. In some embodiments, the pharmaceutical composition of the present application can be formulated into eye drops.

[0142] In some embodiments, the pharmaceutical composition can be formulated for oral administration. Oral formulations can be in the form of a plurality of discrete units, e.g., capsules, pills, cachets, lozenges, or tablets, each containing a predetermined amount of active compound, as a powder or granules, as a solution or suspension in an aqueous or non-aqueous liquid, or as an oil-in-water or water-in-oil emulsion. Excipients for preparing compositions for oral administration are known in the art. Non-limiting suitable excipients include, for example, agar, alginic acid, aluminum hydroxide, benzyl alcohol, benzyl benzoate, 1,3-butylene glycol, carbomer, castor oil, cellulose, cellulose acetate, cocoa butter, corn starch, corn oil, cottonseed oil, crospovidone, diglycerides, ethanol, ethylcellulose, ethyl laurate, ethyl oleate, fatty acid esters, gelatin, germ oil, glucose, glycerol, groundnut oil, hydroxypropyl methylcellulose, isopropyl alcohol, isotonic saline, lactose, magnesium hydroxide, magnesium stearate, malt, mannitol, monoglycerides, olive oil, peanut oil. oil), potassium phosphate, potato starch, povidone, propylene glycol, Ringer's solution, safflower seed oil, sesame oil, sodium carboxymethyl cellulose, sodium phosphate, sodium lauryl sulfate, sodium sorbitol, soybean oil, stearic acid, stearyl fumarate, sucrose, surfactant, talc, tragacanth gum, tetrahydrofurfuryl alcohol, triglyceride, water and mixtures thereof.

[0143] In some embodiments, the pharmaceutical composition is formulated for parenteral administration (e.g., intravenous injection or infusion, subcutaneous or intramuscular injection). The parenteral formulation can be, for example, an aqueous solution, a suspension, or an emulsion. Excipients for preparing parenteral formulations are known in the art. Non-limiting suitable excipients include, for example, 1,3-butanediol, castor oil, corn oil, cottonseed oil, glucose, germ oil, peanut oil, liposomes, oleic acid, olive oil, peanut oil, Ringer's solution, safflower oil, sesame oil, soybean oil, USP

[0144] Or isotonic sodium chloride solution, water and mixtures thereof.

[0145] In some embodiments, the pharmaceutical composition can be formulated for topical administration. A topical preparation comprising one or more salts of the present application can be prepared by mixing one or more salts with various carrier materials or pharmaceutically acceptable excipients. Excipients suitable for preparing topical preparations are known in the art. Some examples of suitable excipients include alcohols, aloe gel, allantoin, glycerol, vitamin A and E oil, mineral oil, PPG2, myristyl propionate lactose, glucose, sucrose, sorbitol, mannitol, starch, gum arabic, calcium phosphate, alginate, tragacanth, gelatin, calcium silicate, microcrystalline cellulose, polyvinyl pyrrolidone, cellulose, sterile water, syrup and methylcellulose. Topical preparations can also include: lubricants such as talc, magnesium stearate and mineral oil; wetting agents; emulsifiers and suspending agents; preservatives, such as methyl benzoate and propyl hydroxybenzoate; sweeteners; coloring agents; perfumes and flavoring agents. When excipient is used as diluent, solid, semisolid or liquid, it can serve as excipient, carrier or matrix of salt.In some embodiments, the topical preparation of the application can be powder, suspension, emulsion, solution, syrup, alcoholic solution, ointment, topical cleanser, cleansing cream, skin gel, toner, mousse, roll-on, aerosol or non-aerosol spray or gel formula and soft gelatin capsule.In some embodiments, pharmaceutical composition can be formulated as local solution, cream, ointment, mousse, gel, toner or powder.In some embodiments, pharmaceutical composition can include excipient, such as water, propylene glycol, citric acid, sodium citrate, tromethamine, alcohol (such as ethanol), preservative etc. For example, exemplary topical formulations comprising one or more salts of the present application can be in the form of topical solutions, such as those having aqueous carriers, alcoholic carriers, aqueous alcoholic carriers, etc., for example, including one or more of the following excipients: water, propylene glycol, citric acid, sodium citrate, tromethamine, alcohol (e.g., ethanol), preservatives, polymers and other excipients. In some embodiments, the topical solution can be formulated as a wipe, which can be contained in a leak-proof, for example, bag with a linear low-density polyethylene (LLDPE) liner. Exemplary topical formulations comprising one or more salts of the present application can be prepared using a formulation similar to U.S. Pat. Nos. 6,433,003, 8,618,160, 9,744,105, 10,052,267, 8,859,610, 9,259,414, 10,004,717,

[0146] Prepared as described in 10,543,192 and 10,548,875.

[0147] The compound / salt of the present application can be used alone, in combination with each other, or in combination with one or more additional therapeutic agents. When used in combination with one or more additional therapeutic agents, the compound or pharmaceutical composition of the present application can be applied to the subject simultaneously with such additional therapeutic agents or in any order. In some embodiments, the pharmaceutical composition can include one or more compounds of the present application and one or more additional therapeutic agents in a single composition. In some embodiments, the pharmaceutical composition comprising one or more compounds of the present application can be included in a kit, which also includes a separate pharmaceutical composition, which includes one or more additional therapeutic agents.

[0148] The pharmaceutical composition may include various amounts of compounds described herein, depending on various factors, such as the intended use, efficacy and selectivity of the compound. In some embodiments, the pharmaceutical composition comprises a therapeutically effective amount of the compound / salt of the present application, for example, for the treatment of hyperhidrosis. In some embodiments, the pharmaceutical composition comprises a therapeutically effective amount of the compound / salt of the present application (for example, for the treatment of hyperhidrosis) and a pharmaceutically acceptable excipient. As used herein, the therapeutically effective amount of the compound / salt of the present application is an amount for effectively treating a disorder, illness or disease (for example, hyperhidrosis) as described herein, which may depend on the recipient of the treatment, the disorder being treated, illness or disease and its severity, the composition containing the compound, the administration time, the route of administration, the duration of treatment, the compound efficacy, its clearance rate and whether another drug is given simultaneously.

[0149] Treatment / Use

[0150] The compounds / salts of the present application have various utilities. For example, the compounds of the present application can be used as therapeutically active substances for treating and / or preventing disorders, conditions or diseases associated with mAChR receptors, such as M3 bodies. Therefore, some embodiments of the present application also relate to methods of using one or more compounds of the present application or the pharmaceutical composition of the present application in a subject in need to treat or prevent disorders, conditions or diseases that may respond to antagonism of mAChRs, such as M3 receptors, for example, for treating hyperhidrosis in a subject in need.

[0151] In some embodiments, the present application provides a method for treating or preventing a disorder, condition or disease that may respond to the antagonism of M3 in a subject in need. In some embodiments, the method comprises administering to the subject an effective amount of a compound of the present application (e.g., Formula I (e.g., Formula I-1, I-1-E1, I-1-E2, I-1-E3, I-1-E4, I-2, I-2-E1, I-2-E2, I-2-E3, I-2-E4, I-3, I-3-E1, I-3-E2,

[0152] Compounds represented by I-3-E3, I-3-E4, I-4, I-4-E1, I-4-E2, I-4-E3, I-4-E4, I-5 or I-6) /

[0153] Salt, any one of Examples 1-12, or any salt shown in Table 1 or Table 2 of the present application, or a pharmaceutically acceptable salt thereof), or an effective amount of the pharmaceutical composition described herein. Disorders, conditions or diseases that may respond to the antagonism of M3 may include any of those described herein and any of those known in the art, such as hyperhidrosis, chronic obstructive pulmonary disease (COPD), mydriasis, abdominal pain, etc.

[0154] In some embodiments, the present application provides a method for inhibiting the activity of mAChRs, such as M3 receptors, in a subject or biological sample. In some embodiments, the method comprises injecting mAchR (e.g.

[0155] M3 receptor) is contacted with an effective amount of a compound of the present application (e.g., a compound / salt represented by Formula I (e.g., Formula I-1, I-1-E1, I-1-E2, I-1-E3, I-1-E4, I-2, I-2-E1, I-2-E2, I-2-E3, I-2-E4, I-3, I-3-E1, I-3-E2, I-3-E3, I-3-E4, I-4, I-4-E1, I-4-E2, I-4-E3, I-4-E4, I-5 or I-6), any one of Examples 1-12, or any salt shown in Table 1 or Table 2 of the present application, or a pharmaceutically acceptable salt thereof) or an effective amount of a pharmaceutical composition described herein.

[0156] Hyperhidrosis is a disorder characterized by excessive sweating, that is, the secretion of sweat in excess of that required to regulate body temperature.

[0157] This condition occurs in up to 1% of the population, with women being the main group affected by this condition. Excessive sweating associated with hyperhidrosis may occur in the hands (palmar hyperhidrosis), armpits (axillary hyperhidrosis), or feet (plantar hyperhidrosis). In the United States alone, 8.8 million people are affected, with 50.8% estimated to suffer from axillary hyperhidrosis and 25-34% suffering from palmar or plantar hyperhidrosis. The root cause of primary hyperhidrosis, also known as idiopathic hyperhidrosis, is not fully understood, but it is generally believed to be closely related to an overactive sympathetic nervous system, as it is well known that sweating is generally controlled by the sympathetic nervous system. Secondary hyperhidrosis can be distinguished from primary hyperhidrosis because it is caused by thyroid or pituitary disorders, diabetes, tumors, gout, menopause, or certain medications.

[0158] Various anticholinergic drugs are described as being effective for treating hyperhidrosis, such as eucatropine derivatives, oxybutynin, propantheline, benztropine, and various glycopyrrolate preparations, see, e.g., U.S. Pat. Nos. 4,720,494, 6,433,003, 8,618,160, 9,744,105, 10,052,267, 8,859,610, 9,259,414, 10,004,717,

[0159] 10,543,192 and 10,548,875, and the prescribing information of Qbrexza revised in June 2018. Compared with these drugs, the compounds or salts of the present application may have similar or better anticholinergic effects and can also be used to treat hyperhidrosis, see, for example, the Examples section.

[0160] In some embodiments, the application provides a method for treating hyperhidrosis in a subject in need. In some embodiments, the method includes administering to the subject a therapeutically effective amount of a compound of the present application (e.g., a compound / salt shown in Formula I (e.g., Formula, I-1, I-1-E1, I-1-E2, I-1-E3, I-1-E4, I-2, I-2-E1, I-2-E2, I-2-E3, I-2-E4, I-3, I-3-E1, I-3-E2, I-3-E3, I-3-E4, I-4, I-4-E1, I-4-E2, I-4-E3, I-4-E4, I-5 or I-6), any one of Examples 1-12, or any salt shown in Table 1 or 2 of the application, or a pharmaceutically acceptable salt thereof), or a therapeutically effective amount of a pharmaceutical composition described in the present application. For the treatment of hyperhidrosis, the administration is typically performed by topical routes. In some embodiments, the hyperhidrosis is primary hyperhidrosis. In some embodiments, the hyperhidrosis is secondary hyperhidrosis. In some embodiments, the hyperhidrosis is primary axillary hyperhidrosis. In some embodiments, the hyperhidrosis is primary palmar hyperhidrosis. In some embodiments, the hyperhidrosis is primary plantar hyperhidrosis.

[0161] Typically, the subject is an adult subject or a pediatric patient 9 years of age or older.

[0162] The treatment methods in the present application are not limited to hyperhidrosis. For example, in some embodiments, the present application also provides a method for treating peptic ulcer in a subject in need thereof, wherein the peptic ulcer involves excessive gastric acid production. In some embodiments, the method includes administering to the subject an effective amount of a compound of the present application (e.g., a compound / salt shown in Formula I (e.g., Formula I-1, I-1-E1, I-1-E2, I-1-E3, I-1-E4, I-2, I-2-E1, I-2-E2, I-2-E3, I-2-E4, I-3, I-3-E1, I-3-E2, I-3-E3, I-3-E4, I-4, I-4-E1, I-4-E2, I-4-E3, I-4-E4, I-5 or I-6), any one of Examples 1-12, or any salt shown in Table 1 or Table 2 of the present application, or a pharmaceutically acceptable salt thereof), or an effective amount of a pharmaceutical composition described herein.

[0163] In some embodiments, the present application also provides a method of reducing salivation in a subject in need thereof, for example, in a child aged 3 to 16 years. In some embodiments, the method comprises administering to the subject an effective amount of a compound of the present application (e.g., Formula I (e.g., Formula I-1, I-1-E1, I-1-E2, I-1-E3, I-1-E4, I-2, I-2-E1, I-2-E2, I-2-E3, I-2-E4, I-3, I-3-E1, I-3-E2, I-3-E3, I-3-E4, I-4,

[0164] I-4-E1, I-4-E2, I-4-E3, I-4-E4, I-5 or I-6), any one of Examples 1-12, or any salt shown in Table 1 or Table 2 of the present application, or a pharmaceutically acceptable salt thereof), or an effective amount of the pharmaceutical composition described in the present application.

[0165] In some embodiments, the application also provides a method for reducing secretions in the stomach or airway of a subject in need. In some embodiments, the method includes administering to the subject an effective amount of a compound of the application (e.g., Formula I (e.g., Formula I-1, I-1-E1, I-1-E2, I-1-E3, I-1-E4, I-2, I-2-E1, I-2-E2, I-2-E3, I-2-E4, I-3, I-3-E1, I-3-E2, I-3-E3, I-3-E4, I-4, I-4-E1, I-4-E2, I-4-E3, I-4-E4, I-5 or I-6) shown in the compound / salt, any one of Examples 1-12, or any salt shown in Table 1 or Table 2 of the application, or a pharmaceutically acceptable salt thereof), or an effective amount of a pharmaceutical composition described in the application.

[0166] In some embodiments, the application also provides a method for protecting the heart and nervous system of a subject in need (e.g., a patient under general anesthesia). In some embodiments, the method includes administering to the subject an effective amount of a compound of the present application (e.g., a compound / salt shown in Formula I (e.g., Formula I-1, I-1-E1, I-1-E2, I-1-E3, I-1-E4, I-2, I-2-E1, I-2-E2, I-2-E3, I-2-E4, I-3, I-3-E1, I-3-E2, I-3-E3, I-3-E4, I-4, I-4-E1, I-4-E2, I-4-E3, I-4-E4, I-5 or I-6), any one of Examples 1-12, or any salt shown in Table 1 or Table 2 of the application, or a pharmaceutically acceptable salt thereof), or an effective amount of a pharmaceutical composition described in the application.

[0167] In some embodiments, the application also provides a method for treating chronic obstructive pulmonary disease (COPD) in a subject in need. In some embodiments, the method includes administering to the subject a therapeutically effective amount of a compound of the application (e.g., a compound / salt shown in Formula I (e.g., Formula I-1, I-1-E1, I-1-E2, I-1-E3, I-1-E4, I-2, I-2-E1, I-2-E2, I-2-E3, I-2-E4, I-3, I-3-E1, I-3-E2, I-3-E3, I-3-E4, I-4, I-4-E1, I-4-E2, I-4-E3, I-4-E4, I-5 or I-6), any one of Examples 1-12, or any salt shown in Table 1 or 2 of the application, or a pharmaceutically acceptable salt thereof), or an effective amount of a pharmaceutical composition described in the application. In some embodiments, the methods of treating COPD described herein may include administering to the subject one or more additional therapeutic agents effective for treating COPD, including any of those known in the art, such as bronchodilators, β-adrenergic agonists, anti-inflammatory agents including but not limited to inhaled steroids, oral steroids, phosphodiesterase-4 inhibitors, JAK inhibitors, TYK2 inhibitors, NLRP3 inhibitors, PI3K inhibitors, SYK inhibitors, BTK inhibitors, IRAK1 and / or IRAK4 inhibitors, theophylline, antibiotics, and the like.

[0168] In some embodiments, the present application also provides a method of inducing pupil dilation in a subject in need thereof. In some embodiments, the method comprises administering to the subject an effective amount of a compound of the present application (e.g., a compound / salt shown in Formula I (e.g., Formula I-1, I-1-E1, I-1-E2, I-1-E3, I-1-E4, I-2, I-2-E1, I-2-E2, I-2-E3, I-2-E4, I-3, I-3-E1, I-3-E2, I-3-E3, I-3-E4, I-4, I-4-E1, I-4-E2, I-4-E3, I-4-E4, I-5 or I-6), any one of Examples 1-12, or any salt shown in Table 1 or Table 2 of the present application, or a pharmaceutically acceptable salt thereof), or an effective amount of a pharmaceutical composition described herein. Typically, methods of inducing mydriasis comprise administering a compound of the present application formulated as eye drops.

[0169] In some embodiments, the application also provides a method for treating abdominal pain in a subject in need. In some embodiments, the method includes administering to the subject an effective amount of the compound of the present application (for example, general formula I (for example, general formula I-1, I-1-E1, I-1-E2, I-1-E3, I-1-E4, I-2, I-2-E1, I-2-E2, I-2-E3, I-2-E4, I-3, I-3-E1, I-3-E2, I-3-E3, I-3-E4, I-4, I-4-E1, I-4-E2, I-4-E3, I-4-E4, I-5 or I-6) shown in the compound / salt, any one of embodiments 1-12 or any salt shown in Table 1 or Table 2 of the application, or its pharmaceutically acceptable salt), or an effective amount of the pharmaceutical composition described in the application. Typically, the method for treating abdominal pain includes oral administration of the compound of the application.

[0170] The administration in the present application method is not limited to any specific route of administration. For example, in some embodiments, the administration can be oral, nasal, topical, transdermal, pulmonary, inhalation, buccal, sublingual, intraperitoneal, subcutaneous, intramuscular, intravenous, rectal, intrathoracic, intrathecal and through the parenteral tract. In some embodiments, the administration is topical administration. In some embodiments, the administration is oral administration. In some embodiments, the administration is parenteral administration.

[0171] As discussed herein, the compounds of the present application can be used as monotherapy or combination therapy. In some embodiments according to the methods described herein, the compounds of the present application can be administered as the sole active ingredient. In some embodiments, one or more compounds of the present application can be used in combination with an additional therapy, for example, an additional therapy that is effective in treating hyperhidrosis. In some embodiments according to the methods described herein, one or more compounds of the present application can also be co-administered to a subject in need with another therapeutic agent, for example, an agent that is effective in treating hyperhidrosis, simultaneously or sequentially in any order.

[0172] The dosage regimen, including the dosages of the methods described herein, can be varied and adjusted, depending on the subject being treated, the disorder, condition or disease being treated and its severity, the composition containing the compound, the time of administration, the route of administration, the duration of treatment, the potency of the compound, the clearance rate, and whether it is administered in combination with another drug.

[0173] definition

[0174] It is to be understood that all groups and combinations thereof maintain appropriate valences.

[0175] It is also to be understood that a specific embodiment of a variable portion in the present application may be the same as or different from another specific embodiment having the same identifier.

[0176] Suitable groups for compounds of formulae I and II or subformulae thereof, as applicable, are selected independently.

[0177] The embodiments described in this application can be combined. Such combinations are contemplated and within the scope of this application. For example, it is contemplated that R of Formula I 1 , R 2 , R 3 , R 4 , L 1 , X - Any one or more definitions of and j can be combined with other R 1 , R 2 , R 3 , R 4 , L 1 , X - and j, any one or more of the definitions may be combined as applicable, and the compounds resulting from the combination are within the scope of the present application. Combinations of other variables in other formulae should be similarly construed.

[0178] symbol Whether used as a bond or shown perpendicular to (or otherwise crossing) a bond, it indicates the point at which the portion shown is attached to the rest of the molecule. It should be noted that one or more groups that are directly attached can be shown outside the symbol to indicate connectivity, as understood by those skilled in the art.

[0179] The definitions of specific functional groups and chemical terms are described in more detail below. Chemical elements are based on the Periodic Table, CAS version, Handbook of Chemistry and Physics 75 th Ed. Inside cover, specific functional groups are generally defined as in this application. In addition, the general principles of organic chemistry, as well as specific functional groups and reactivity, are described in Thomas Sorrell's book Organic Chemistry, University Science Books, Sausalito, 1999; Smith and March's book March's Advanced Organic Chemistry, 5th Edition, John Wiley & Sons, Inc. Publishing Company, New York, 2001; Larock's book Comprehensive Organic Transformations, VCH Publishers, Inc. Publishing Company, New York, 1989; and Carruthers' book Some Modern Methods of Organic Synthesis, 3rd Edition, Cambridge University Press, Cambridge, 1987. This application is not intended to be limited in any way by the list of exemplary substituents described in this application.

[0180] The compounds described herein may contain one or more asymmetric centers and may therefore exist in various isomeric forms, for example, enantiomers and / or diastereomers. For example, the compounds described herein may be in the form of individual enantiomers, diastereomers, or geometric isomers, or may be in the form of a mixture of stereoisomers, including racemic mixtures and mixtures enriched in one or more stereoisomers. Isomers may be separated from the mixture by methods known to those skilled in the art, including chiral high performance liquid chromatography (HPLC) and the formation and crystallization of chiral salts; or the dominant isomer may be prepared by asymmetric synthesis.

[0181] See, for example, Jacques et al., Enantiomers, Racemates and Resolutions (Wiley Interscience, New York, 1981); Wilen et al., Tetrahedron 33:2725 (1977); Eliel, Stereochemistry of Carbon Compounds (McGraw-Hill, NY, 1962); and Wilen, Tables of Resolving

[0182] Agents and Optical Resolutions p. 268 (EL E Liel, Ed., Univ. of Notre Dame Press, Notre Dame, IN 1972). The present application also includes the compounds described herein as individual isomers substantially free of other isomers, or as mixtures of various isomers including racemic mixtures. When stereochemistry is specifically drawn, unless the context contradicts, it is understood that the compound may be present primarily as the drawn stereoisomer, e.g., less than 20%, less than 10%, less than 5%, less than 1%, or with undetectable amounts of other stereoisomers, with respect to that particular chiral center or axial chirality. In view of the present application, one skilled in the art can determine the presence and / or

[0183] or amount, including by using chiral HPLC.

[0184] When a range of values ​​is listed, it is intended to include every value and subrange within that range. For example, “C 1-6 ”

[0185] Designed to cover C1, C2, C3, C4, C5, C6, C 1-6 , C 1-5 , C 1-4 , C 1-3 , C 1-2 , C 2-6 , C 2-5 , C 2-4 , C 2-3 , C 3-6 , C 3-5 , C 3-4 , C 4-6 , C 4-5 and C 5-6 .

[0186] As used herein, the term "compound of the present application" or "salt of the present application" refers to a salt of the present application according to Formula I (e.g., I-1, I-1-E1, I-1-E2, I-1-E3, I-1-E4, I-2, I-2-E1, I-2-E2, I-2-E3, I-2-E4, I-3, I-3-E1, I-3-E2, I-3-E3, I-3-E4, I-4, I-4-E1, I-4-E2, I-4-E3, I-4-E4, I-5, or I-6), Formula II (e.g., Formula I I-1 or II-2), any one of Examples 1-12, or any salt shown in Table 1 or Table 2 of the present application, compounds / salts, isotope-labeled compounds thereof (e.g., deuterated analogs in which one or more hydrogen atoms are replaced by deuterium atoms having an abundance higher than their natural abundance), possible regioisomers, possible stereoisomers (including diastereomers, enantiomers, and racemic mixtures), tautomers thereof, conformational isomers thereof, and / or possible pharmaceutically acceptable salts (e.g., acid addition salts such as hydrochlorides, or base addition salts such as sodium salts). Hydrates and solvates of the compounds of the present application are considered to be compositions of the present application, in which the compounds are combined with water or a solvent, respectively.

[0187] The compounds of the present application may exist in isotopically labeled or isotopically enriched form, containing one or more atoms whose atomic mass or mass number is different from the atomic mass or mass number most abundant in nature. Isotopes may be radioactive or non-radioactive isotopes. Isotopes of atoms such as hydrogen, carbon, phosphorus, sulfur, fluorine, chlorine, iodine, etc. include but are not limited to 2 H. 3 H. 13 C. 14 C. 15 N. 18 O. 32 P. 35 S, 18 F. 36 Cl and 125 I. Compounds containing other isotopes of these and / or other atoms are within the scope of the invention.

[0188] As used herein, the phrases "administering" a compound or salt, "administering" a compound or salt,

[0189] or other variations thereof refers to providing the compound or salt, or a prodrug of the compound or salt, to a subject in need of treatment.

[0190] As used herein, the term "alkyl" used alone or as part of another group refers to a straight or branched aliphatic saturated hydrocarbon. In some embodiments, an alkyl group may include one to twelve carbon atoms (i.e., C 1-12In one embodiment, the alkyl group is a straight chain C 1-10 In another embodiment, the alkyl group is a branched C 3-10 In another embodiment, the alkyl group is a straight chain C 1-6 In another embodiment, the alkyl group is a branched C 3-6 In another embodiment, the alkyl group is a straight chain C 1-4 Alkyl. For example, C 1-4 Alkyl includes methyl, ethyl, propyl (n-propyl), isopropyl, butyl (n-butyl), sec-butyl, tert-butyl and isobutyl. In this application, the term "alkylene" used alone or as part of another group refers to a divalent group derived from an alkyl group. For example,

[0191] Non-limiting straight chain alkylene groups include -CH2-CH2-CH2-CH2-, -CH2-CH2-CH2-, -CH2-CH2-, and the like.

[0192] In the present application, the term "alkenyl" used alone or as part of another group refers to a straight or branched aliphatic hydrocarbon containing one or more, for example, one, two or three carbon-carbon double bonds. In one embodiment, alkenyl is C 2-6 In another embodiment, alkenyl is C 2-4 Alkenyl. Non-limiting exemplary alkenyl groups include ethenyl, propenyl, isopropenyl, butenyl, sec-butenyl, pentenyl, and hexenyl.

[0193] In this application, the term "alkynyl" used alone or as part of another group refers to a straight or branched aliphatic hydrocarbon containing one or more, for example, one to three, carbon-carbon triple bonds. In one embodiment, the alkynyl group has one carbon-carbon triple bond. In one embodiment, the alkynyl group is C 2-6 In another embodiment, alkynyl is C 2-4 Alkynyl. Non-limiting exemplary alkynyl groups include ethynyl, propynyl, butynyl, 2-butynyl, pentynyl, and hexynyl.

[0194] In this application, the term "alkoxy" used alone or as part of another group refers to a group of the general formula OR a1 A group in which R a1 It is an alkyl group.

[0195] In this application, the term "cycloalkoxy" as used alone or as part of another group

[0196] Refers to the general formula OR a1 A group in which R a1 It is a cycloalkyl group.

[0197] In this application, the term "haloalkyl" as used alone or as part of another group

[0198] refers to an alkyl group substituted by one or more fluorine, chlorine, bromine and / or iodine atoms. In a preferred embodiment, a haloalkyl group is an alkyl group substituted by one, two or three fluorine atoms. In one embodiment, a haloalkyl group is C 1-10 In one embodiment, the haloalkyl group is C 1-6 In one embodiment, the haloalkyl group is C 1-4 Halogenated alkyl.

[0199] In this application, unless otherwise indicated, the term "heteroalkyl" by itself or in combination with another term refers to a stable straight or branched chain alkyl group having, for example, 2 to 14 carbons, such as 2 to 10 carbons, in the chain, one or more of which is substituted with a heteroatom selected from S, O, P, and N, and wherein the nitrogen, phosphorus, and sulfur atoms may be optionally oxidized and the nitrogen heteroatom may be optionally quaternized. The heteroatoms S, O, P, and N may be located at any interior position of the heteroalkyl group, or at the position where the alkyl group is attached to the rest of the molecule. When a heteroalkyl group is referred to as being substituted, the substituent may replace the carbon atoms and / or heteroatoms attached to the heteroalkyl group. In some embodiments, the heteroalkyl group is C 1-4 Heteroalkyl refers to a heteroalkyl group having 1 to 4 carbon atoms as defined in the present application. 1-4Examples of heteroalkyl groups include, but are not limited to, C4 heteroalkyl groups such as -CH2-CH2-N(CH3)-CH3, C3 heteroalkyl groups such as -CH2-CH2-O-CH3, CH2-CH2-NH-CH3, -CH2-S-CH2-CH3, -CH2-CH2-S(O)-CH3, -CH2-CH2-S(O)2-CH3, C2 heteroalkyl groups such as -CH2-CH2-OH, -CH2-CH2-NH2, -CH2-NH(CH3), -O-CH2-CH3, and C1 heteroalkyl groups such as -CH2-OH, -CH2-NH2, -O-CH3. Similarly, the term "heteroalkylene" by itself or as part of another substituent refers to a divalent radical derived from an alkyl group, such as, but not limited to, -CH2-CH2-O-CH2-CH2- and -O-CH2-CH2-NH-CH2-. For heteroalkylene, heteroatoms may also occupy one or both chain ends (e.g., alkyleneoxy, alkylenedioxy, alkyleneamino, alkylenediamino, etc.). Further, for alkylene and heteroalkylene linking groups, the direction in which the general formula of the linking group is written does not imply the orientation of the linking group. When "heteroalkyl" is cited and then a specific heteroalkyl group such as -NR'R" is cited, it should be understood that the terms "heteroalkyl" and -NR'R" are not redundant or mutually exclusive. On the contrary, the specific heteroalkyl group is cited for greater clarity. Therefore, the term "heteroalkyl" should not be interpreted in this application to exclude specific heteroalkyl groups, such as -NR'R", etc.

[0200] "Carbocyclyl" or "carbocycle" used alone or as part of another group refers to a non-aromatic ring system having at least 3 carbon atoms, such as 3 to 10 ring carbon atoms ("C 3-10 The term "carbocyclyl" refers to a group of non-aromatic cyclic hydrocarbon groups having zero heteroatoms and a monocyclic ("monocyclic carbocyclyl") ring system. The carbocyclyl group may be monocyclic ("monocyclic carbocyclyl") or contain a fused, bridged or spiro ring system, such as a bicyclic system ("bicyclic carbocyclyl") and may be saturated or may be partially unsaturated. Non-limiting exemplary carbocyclyl groups include cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, cyclooctyl, norbornyl, decalinyl, adamantyl, cyclopentenyl and cyclohexenyl. As used herein, the term "carbocyclylene" used alone or as part of another group refers to a divalent radical derived from a carbocyclyl group as defined herein.

[0201] In some embodiments, a "carbocyclyl" is fully saturated, also known as a cycloalkyl. In some embodiments, a cycloalkyl may have 3 to 10 ring carbon atoms ("C 3-10 In a preferred embodiment, the cycloalkyl group is a monocyclic ring. In the present application, the term "cycloalkylene" used alone or as part of another group refers to a divalent group derived from a cycloalkyl group, for example, wait.

[0202] "Heterocyclyl" or "heterocycle" used alone or as part of another group refers to a group of a 3-membered or more, e.g., 3- to 14-membered, non-aromatic ring system having ring carbon atoms and at least one ring heteroatom, e.g., 1 to 4 ring heteroatoms, each of which is independently selected from nitrogen, oxygen, sulfur, boron, phosphorus, and silicon. In heterocyclyls containing one or more nitrogen atoms, the point of attachment may be a carbon atom or a nitrogen atom as long as valence permits. Heterocyclyls may be monocyclic ("monocyclic heterocyclyl") or may be fused, bridged, or spirocyclic systems such as bicyclic systems ("bicyclic heterocyclyl") and may be saturated or may be partially unsaturated. Heterocyclyl bicyclic systems may include one or more heteroatoms in one or both rings, and the point of attachment may be on either ring. As used herein, the term "heterocyclylene" used alone or as part of another group refers to a divalent group derived from a heterocyclyl defined herein. A heterocyclyl or heterocyclylene group may optionally be attached to the remainder of the molecule via a carbon atom or a nitrogen atom.

[0203] Exemplary 3-membered heterocyclic groups containing one heteroatom include, but are not limited to, aziridine, oxirane, and thiirane. Exemplary 4-membered heterocyclic groups containing one heteroatom include, but are not limited to, azetidinyl, oxetanyl, and thiirane. Exemplary 5-membered heterocyclic groups containing one heteroatom include, but are not limited to, tetrahydrofuranyl, dihydrofuranyl, tetrahydrothienyl, dihydrothienyl, pyrrolidinyl, dihydropyrrolyl, and pyrrolyl-2,5-dione. Exemplary 5-membered heterocyclic groups containing two heteroatoms include, but are not limited to, dioxa-lanyl, oxathia-lanyl, dithia-lanyl, and oxazolidin-2-one. Exemplary 5-membered heterocyclic groups containing three heteroatoms include, but are not limited to, triazolinyl, oxadiazolinyl, and thiadiazolinyl. Exemplary 6-membered heterocyclic groups containing one heteroatom include, but are not limited to, piperidinyl, tetrahydropyranyl, dihydropyridinyl, and thienyl. Exemplary 6-membered heterocyclic groups containing two heteroatoms include, but are not limited to, piperazinyl, morpholinyl, dithienyl, and dioxanyl. Exemplary 6-membered heterocyclic groups containing two heteroatoms include, but are not limited to, triazine. Exemplary 7-membered heterocyclic groups containing one heteroatom include, but are not limited to, azepanyl, oxepane, and thiepanyl. Exemplary 8-membered heterocyclic groups containing one heteroatom include, but are not limited to, azooctanyl, oxoctanyl, and thieoctanyl. Exemplary 5-membered heterocyclic groups fused to C6 aryl rings (also referred to herein as 5,6-bicyclic heterocycles) include, but are not limited to, indolinyl, isoindolinyl, dihydrobenzofuranyl, dihydrobenzothienyl, benzoxazoline, and the like. Exemplary 6-membered heterocyclic groups fused to aryl rings (also referred to herein as 6,6-bicyclic heterocycles) include, but are not limited to, tetrahydroquinolinyl, tetrahydroisoquinolinyl, and the like.

[0204] "Aryl" used alone or as part of another group refers to a monocyclic or polycyclic (e.g., bicyclic or tricyclic) 4n+2 aromatic ring system (e.g., sharing 6, 10 or 14 π electrons in a cyclic arrangement) having 6-14 ring carbon atoms and zero heteroatoms provided in the aromatic ring system ("C 6-14 In some embodiments, an aryl group has six ring carbon atoms (a "C6 aryl"; e.g., phenyl). In some embodiments, an aryl group has ten ring carbon atoms (a "C 10 In some embodiments, an aryl group has fourteen ring carbon atoms ("C 14 As used herein, the term "arylene" used alone or as part of another group refers to a divalent radical derived from an aryl group as defined herein.

[0205] "Aralkyl" used alone or as part of another group refers to an alkyl group substituted with one or more aryl groups, preferably with one aryl group. Examples of aralkyl groups include benzyl, phenethyl, etc. When an aralkyl group is referred to as optionally substituted, either the alkyl portion or the aryl portion of the aralkyl group may be optionally substituted.

[0206] "Heteroaryl" used alone or as part of another group refers to a group of a 5-14 membered monocyclic, bicyclic, or tricyclic 4n+2 aromatic ring system (e.g., having 6 or 10 π electrons shared in a cyclic arrangement) ("5-14 membered heteroaryl") having ring carbon atoms provided in the aromatic ring system and at least one, preferably 1-4, ring heteroatoms, wherein each heteroatom is independently selected from nitrogen, oxygen, and sulfur. In heteroaryl groups containing one or more nitrogen atoms, the point of attachment can be a carbon atom or a nitrogen atom as long as the valence permits. The heteroaryl bicyclic ring system can contain one or more heteroatoms in one or both rings. For cyclic heteroaryl groups that do not contain heteroatoms on one ring (e.g., indolyl, quinolyl, etc.), the point of attachment can be on either ring, i.e., on the ring with heteroatoms (e.g., 2-indolyl) or on the ring without heteroatoms (e.g., 5-indolyl). As used herein, the term "heteroarylene" used alone or as part of another group refers to a divalent radical derived from a heteroaryl group as defined herein.

[0207] Exemplary 5-membered heteroaryl groups containing one heteroatom include, but are not limited to, pyrrolyl, furanyl, and thienyl. Exemplary 5-membered heteroaryl groups containing two heteroatoms include, but are not limited to, imidazolyl, pyrazolyl, oxazolyl, isoxazolyl, thiazolyl, and isothiazolyl. Exemplary 5-membered heteroaryl groups containing three heteroatoms include, but are not limited to, triazolyl, oxadiazolyl, and thiadiazolyl. Exemplary 5-membered heteroaryl groups containing four heteroatoms include, but are not limited to, tetrazolyl. Exemplary 6-membered heteroaryl groups containing one heteroatom include, but are not limited to, pyridinyl. Exemplary 6-membered heteroaryl groups containing two heteroatoms include, but are not limited to, pyridazinyl, pyrimidinyl, and pyrazinyl. Exemplary 6-membered heteroaryl groups containing three or four heteroatoms include, but are not limited to, triazinyl and tetrazinyl, respectively. Exemplary 7-membered heteroaryl groups containing one heteroatom include, but are not limited to, azacycloheptatrienyl, oxacycloheptatrienyl, and thiacycloheptatrienyl. Exemplary 5,6-bicyclic heteroaryl groups include, but are not limited to, indolyl, isoindolyl, indazolyl, benzotriazolyl, benzothiophenyl, isobenzothiophenyl, benzofuranyl, benzisofuranyl, benzimidazolyl, benzoxazolyl, benzisoxazolyl, benzoxadiazolyl, benzothiazolyl, benzisothiazolyl, benzothiadiazolyl, indolizinyl, and purinyl. Exemplary 6,6-bicyclic heteroaryl groups include, but are not limited to, naphthyridinyl, pteridinyl, quinolyl, isoquinolyl, cinnolinyl, quinoxalinyl, phthalazinyl, and quinazolinyl.

[0208] "Heteroaralkyl" used alone or as part of another group refers to an alkyl group substituted with one or more aryl groups, preferably with one aryl group. When the heteroaralkyl group is referred to as being optionally substituted, either the alkyl portion or the heteroaryl portion of the heteroaralkyl group may be optionally substituted.

[0209] An "optionally substituted" group, such as an optionally substituted alkyl, an optionally substituted alkenyl, an optionally substituted alkynyl, an optionally substituted carbocyclic radical, an optionally substituted heterocyclic radical, an optionally substituted aryl and an optionally substituted heteroaryl refer to the corresponding groups that are unsubstituted or substituted. Generally speaking, the term "substituted", whether preceded by the term "optionally", refers to at least one hydrogen present in a group (e.g., carbon or nitrogen atom) being replaced with a substituent that is allowed, for example, the substituent produces a stable compound after substitution, for example, the compound will not spontaneously be transformed, for example, by rearrangement, cyclization, elimination or other reactions. Unless otherwise indicated, a "substituted" group has a substituent at one or more substitutable positions of the group, and when more than one position in any given structure is substituted, the substituent may be the same or different at each position. Typically, when substituted, the optionally substituted group of the application may be substituted by 1-5 substituents. The substituent may be a carbon atom substituent, a nitrogen atom substituent, an oxygen atom substituent or a sulfur atom substituent, as the case may be. Two optional substituents can be connected to form an optionally substituted ring structure, such as a carbocyclic group (e.g., cycloalkyl), heteroaryl, aryl or heteroaryl ring. Substitution can occur on any available carbon, oxygen or nitrogen atom, and can form a spirocycle. Typically, substitution here will not produce OO, ON, SS, SN (except SO2-N key), heteroatom-halogen or-C (O)-S key or three or more continuous heteroatoms, but O-SO2-O, O-SO2-N and

[0210] The exception is N-SO2-N, except that some such bonds or linkages may be permitted if in a stable aromatic system.

[0211] In a broad sense, the substituents permitted in the present application include substituents of acyclic and cyclic, branched and unbranched, carbocyclic and heterocyclic, aromatic and non-aromatic organic compounds of organic compounds. For suitable organic compounds, the substituents permitted may be one or more and may be the same or different. For the purposes of the present application, heteroatoms such as nitrogen may have hydrogen substituents and / or any permitted substituents of the organic compounds described in the present application that satisfy the heteroatom valences. Substituents may include any of the substituents described herein, such as halogen, hydroxy, carbonyl (e.g., carboxyl, alkoxycarbonyl, formyl or acyl), thiocarbonyl (e.g., thioester, thioacetate or thioformate), alkoxy, cycloalkyloxy, phosphoryl, phosphate, phosphonate, phosphinate, amino, amido, amidino, imino, cyano, nitro, azido, sulfhydryl, alkylthio, sulfate, sulfonate, aminosulfonyl, sulfonamido, sulfonyl, heterocyclyl, aralkyl, aryl or heteroaryl, each of which may be substituted if appropriate.

[0212] , heteroaryl, -alkylene-aryl, -arylene-alkyl, -alkylene-heteroaryl, -alkenylene-heteroaryl,

[0213] -alkynylene-heteroaryl, -OH, hydroxyalkyl, haloalkyl, -O-alkyl, -O-haloalkyl, -alkylene-O-

[0214] Alkyl, -O-aryl, -O-alkylene-aryl, acyl, -C(O)-aryl, halogen, -NO2, -CN, -SF5,

[0215] -C(O)OH, -C(O)O-alkyl, -C(O)O-aryl, -C(O)O-alkylene-aryl, -S(O)-alkyl, -S(O)2-alkyl, -S(O)-aryl, -S(O)2-aryl, -S(O)-heteroaryl, -S(O)2-heteroaryl, -S-alkyl, -S-aryl,

[0216] -S-heteroaryl, -S-alkylene-aryl, -S-alkylene-heteroaryl, -S(O)2-alkylene-aryl, -S(O)2-alkylene-heteroaryl, cycloalkyl, heterocycloalkyl, -OC(O)-alkyl, -OC(O)-aryl, -OC(O)-cycloalkyl,

[0217] -C(=N-CN)-NH2, -C(=NH)-NH2, -C(=NH)-NH(alkyl), -N(Y1)(Y2), -alkylene-N(Y1)(Y2),

[0218] -C(O)N(Y1)(Y2) and -S(O)2N(Y1)(Y2), wherein Y1 and Y2 may be the same or different and are independently selected from hydrogen, alkyl, aryl, cycloalkyl and -alkylene-aryl.

[0219] Some examples of suitable substituents include, but are not limited to, (C1-C8)alkyl, (C2-C8)alkenyl, (C2-C8)alkynyl, (C3-C 10 ) cycloalkyl, halogen (F, Cl, Br or I), halo (C1-C8) alkyl (such as but not limited to -CF3),

[0220] -O-(C1-C8)alkyl, -OH, -S-(C1-C8)alkyl, -SH, -NH(C1-C8)alkyl, -N((C1-C8)alkyl)2, -NH2, -C(O)NH2, -C(O)NH(C1-C8)alkyl, -C(O)N((C1-C8)alkyl)2, -NHC(O)H,

[0221] -NHC(O)(C1-C8)alkyl, -NHC(O)(C3-C8)cycloalkyl, -N((C1-C8)alkyl)C(O)H, -N((C1-C8)alkyl)C(O)(C1-C8)alkyl, -NHC(O)NH2, -NHC(O)NH(C1-C8)alkyl, -N((C1-C8)alkyl)C(O)NH2 group, -NHC(O)N((C1-C8)alkyl)2 group, -N((C1-C8)alkyl)C(O)N((C1-C8)alkyl)2 group, -N((C1-C8)alkyl)C(O)NH((C1-C8)alkyl), -C(O)H, -C(O)(C1-C8)alkyl, -CN,

[0222] -NO2, -S(O)(C1-C8)alkyl, -S(O)2(C1-C8)alkyl, -S(O)2N((C1-C8)alkyl)2 group,

[0223] -S(O)2NH(C1-C8)alkyl, -S(O)2NH(C3-C8)cycloalkyl, -S(O)2NH2 group, -NHS(O)2(C1-C8)alkyl, -N((C1-C8)alkyl)S(O)2(C1-C8)alkyl, -(C1-C8)alkyl-O-(C1-C8)alkyl, -O-(C1-C8)alkyl-O-(C1-C8)alkyl, -C(O)OH, -C(O)O(C1-C8)alkyl, NHOH, NHO(C1-C8)alkyl,

[0224] -O-halo(C1-C8)alkyl (for example, but not limited to -OCF3), -S(O)2-halo(C1-C8)alkyl (for example, but not limited to -S(O)2CF3), -S-halo(C1-C8)alkyl (for example, but not limited to -SCF3), -(C1-C6)heterocycle (for example, but not limited to pyrrolidine, tetrahydrofuran, pyran or morpholine), -(C1-C6)heteroaryl (for example, but not limited to tetrazole, imidazole, furan, pyrazine or pyrazole), -phenyl, -NHC(O)O-(C1-C6)alkyl, -N((C1-C6)alkyl)C(O)O-(C1-C6)alkyl, -C(=NH)-(C1-C6)alkyl, -C(=NOH)-(C1-C6)alkyl, or

[0225] -C(=N-O-(C1-C6)alkyl)-(C1-C6)alkyl.

[0226] Exemplary carbon atom substituents include, but are not limited to, halogen, -CN, -NO2, -N3, hydroxy, alkoxy, cycloalkoxy, aryloxy, amino, monoalkylamino, dialkylamino, amide, sulfonamide, thiol, acyl, carboxylic acid, ester, sulfone, sulfoxide, alkyl, haloalkyl, alkenyl, alkynyl, C3-10 Carbocyclic group, C 6-10 aryl, 3-10 membered heterocyclic group, 5-10 membered heteroaryl, etc. For example, exemplary carbon atom substituents may include F, Cl, -CN, SO2H, -SO3H, OH, -OC 1-6 Alkyl, -NH2, -N(C 1-6 Alkyl)2, -NH(C 1-6 alkyl),

[0227] -SH, -SC 1-6 Alkyl, -C(=O)(C 1-6 alkyl), -CO2H, -CO2(C 1-6 alkyl), -OC(=O)(C 1-6 alkyl),

[0228] -OCO2(C 1-6 alkyl), -C(=O)NH2, -C(=O)N(C 1-6 alkyl)2, -OC(=O)NH(C 1-6 alkyl),

[0229] -NHC(=O)(C 1-6 Alkyl), -N(C 1-6 alkyl)C(=O)(C 1-6 Alkyl), -NHCO2(C 1-6 alkyl),

[0230] -NHC(=O)N(C 1-6 Alkyl)2, -NHC(=O)NH(C 1-6 alkyl), -NHC(=O)NH2, -NHSO2(C 1-6 Alkyl), -SO2N(C 1-6 Alkyl)2, -SO2NH(C 1-6 Alkyl), -SO2NH2, -SO2C 1-6 Alkyl, -SO2OC 1-6 Alkyl, -OSO2C 1-6 Alkyl, -SOC 1-6 Alkyl, C 1-6 Alkyl, C 1-6 Haloalkyl, C 2-6 Alkenyl, C 2-6 Alkynyl, C 3-10 Carbocyclic group, C 6-10 aryl, 3-10 membered heterocyclyl, 5-10 membered heteroaryl; or two geminal substituents may be linked to form =0.

[0231] Where valence permits, the nitrogen atoms may be substituted or unsubstituted and include primary, secondary, tertiary, and quaternary nitrogen atoms. Exemplary nitrogen atom substituents include, but are not limited to, hydrogen, acyl, ester, sulfone, sulfoxide, C 1-10 Alkyl, C 1-10 Haloalkyl, C 2-10 Alkenyl, C 2-10 Alkynyl, C 3-10 Carbocyclic group, 3-14 membered heterocyclic group,

[0232] C 6-14 Aryl and 5-14 membered heteroaryl, or two substituents attached to the nitrogen atom are connected to form a 3-14 membered heterocyclyl or 5-14 membered heteroaryl ring, wherein each alkyl, alkenyl, alkynyl, carbocyclyl, heterocyclyl, aryl and heteroaryl may be further substituted as defined herein. In certain embodiments, the substituent present on the nitrogen atom is a nitrogen protecting group (also referred to as an amino protecting group). Nitrogen protecting groups are well known in the art and include

[0233] Those described in detail in Protective Groups in Organic Synthesis, TW Greene and PGM Wuts, 3rd edition, John Wiley & Sons, 1999, are incorporated herein by reference. Exemplary nitrogen protecting groups include, but are not limited to, those that form carbamates, such as benzyloxycarbonyl (Cbz) groups, p-methoxybenzylcarbonyl (Moz or MeOZ) groups, tert-butoxycarbonyl (BOC) groups, Troc, 9-fluorenylmethoxycarbonyl (Fmoc) groups, etc.; those that form amides, such as acetyl, benzoyl, etc.; those that form benzylamines, such as benzyl, p-methoxybenzyl, 3,4-dimethoxybenzyl, etc.; those that form sulfonamides, such as toluenesulfonyl, nitrobenzenesulfonyl, etc.; and other protecting groups, such as p-methoxyphenyl, etc.

[0234] Exemplary oxygen atom substituents include, but are not limited to, acyl, ester, sulfonate, C 1-10 Alkyl, C 1-10 Haloalkyl, C 2-10 Alkenyl, C 2-10 Alkynyl, C 3-10 Carbocyclic group, 3-14 membered heterocyclic group, C 6-14Aryl and 5-14 yuan heteroaryl, wherein each alkyl, alkenyl, alkynyl, carbocyclic radical, heterocyclic radical, aryl and heteroaryl can be further substituted as defined in the application.In certain embodiments, the oxygen atom substituent present on the oxygen atom is an oxygen protecting group (also referred to as a hydroxy protecting group).Oxygen protecting groups are well known in the art, are included in " Protective Groups in Organic Synthesis ", TW Greene and PGM Wuts, the 3rd edition, John Wiley & Sons, those oxygen protecting groups described in detail in 1999, are incorporated herein by reference at this. Exemplary oxygen protecting groups include, but are not limited to, those that form alkyl ethers or substituted alkyl ethers, such as methyl, allyl, benzyl, substituted benzyl (e.g., 4-methoxybenzyl), methoxymethyl (MOM), benzyloxymethyl (BOM), 2-methoxyethoxymethyl (MEM), and the like; those that form silyl ethers, such as trimethylsilyl (TMS), triethylsilyl (TES), triisopropylsilyl (TIPS), tert-butyldimethylsilyl (TBDMS), and the like; those that form acetals or ketals, such as tetrahydropyranyl (THP); those that form esters, such as formates, acetates, chloroacetates, dichloroacetates, trichloroacetates, trifluoroacetates, methoxyacetates, and the like; those that form carbonates or sulfonates, such as methyl sulfonate (mesylate), benzylsulfonate, tosylate (Ts), and the like.

[0235] Unless expressly stated to the contrary, combinations of substituents and / or variables are permissible only if such combinations are chemically permitted and result in stable compounds. A "stable" compound is one that can be prepared and isolated and whose structure and properties remain or are capable of being maintained substantially unchanged for a period of time sufficient to permit use of the compound for the purposes described herein (e.g., therapeutic administration to a subject).

[0236] In some embodiments, the "optionally substituted" alkyl, alkylene, heteroalkyl, heteroalkylene, alkenyl, alkynyl, carbocyclyl, carbocyclylene, cycloalkyl, cycloalkylene, alkoxy, cycloalkyloxy, heterocyclyl or heterocyclylene in the present application can be each independently unsubstituted or substituted with 1, 2, 3 or 4 substituents independently selected from the following: F, Cl, -OH, protected hydroxy, oxo (if applicable), NH2, protected amino, NH(C 1-4 alkyl) or its protected derivatives, N(C 1-4 Alkyl)(C 1-4 Alkyl), C 1-4 Alkyl, C 2-4 Alkenyl, C 2-4 Alkynyl, C 1-4 Alkoxy, C3-6 Cycloalkyl, C 3-6 cycloalkyloxy, phenyl, 5- or 6-membered heteroaryl containing 1, 2 or 3 ring heteroatoms independently selected from O, S and N, 3-7-membered heterocyclyl containing 1 or 2 ring heteroatoms independently selected from O, S and N, wherein each of alkyl, alkenyl, alkynyl, alkoxy, cycloalkyl, cycloalkyloxy, phenyl, heteroaryl and heterocyclyl is optionally substituted by 1, 2 or 3 independently selected from F,

[0237] -OH, oxo (if applicable), C 1-4 Alkyl, fluorine-substituted C 1-4 Alkyl (e.g., CF3), C 1-4 Alkoxy and fluorine substituted C 1-4 In some embodiments, the "optionally substituted" aryl, arylene, heteroaryl or heteroarylene group in the present application can be each independently unsubstituted or substituted with 1, 2, 3 or 4 substituents independently selected from the following: F, Cl, -OH, -CN, NH2, protected amino, NH(C 1-4 alkyl) or its protected derivatives, N(C 1-4 Alkyl)(C 1-4 alkyl), -S(=O)(C 1-4 alkyl),

[0238] -SO2(C 1-4 Alkyl), C 1-4 Alkyl, C 2-4 Alkenyl, C 2-4 Alkynyl, C 1-4 Alkoxy, C 3-6 Cycloalkyl, C 3-6 cycloalkyloxy, phenyl, 5- or 6-membered heteroaryl containing 1, 2 or 3 ring heteroatoms independently selected from O, S and N, 3-7-membered heterocyclyl containing 1 or 2 ring heteroatoms independently selected from O, S and N, wherein each of alkyl, alkenyl, alkynyl, alkoxy, cycloalkyl, cycloalkyloxy, phenyl, heteroaryl and heterocyclyl is optionally substituted by 1, 2 or 3 independently selected from F, -OH, oxo (if applicable), C 1-4 Alkyl, fluorine-substituted C 1-4 Alkyl, C 1-4 Alkoxy and fluorine substituted C 1-4 The substituents of the alkoxy group are substituted.

[0239] "Halo" or "halogen" refers to fluorine (fluoro, -F), chlorine (chloro,

[0240] -Cl), bromine (bromo, -Br) or iodine (iodo, -I).

[0241] The term "leaving group" is given its ordinary meaning in the field of synthetic organic chemistry and refers to an atom or group capable of being displaced by a nucleophile. See, for example, Smith, March Advanced Organic Chemistry.

[0242] 6th edition. (501-502). Examples of suitable leaving groups include, but are not limited to, halogens (e.g., F, Cl,

[0243] Br or I (iodine)), alkoxycarbonyloxy, aryloxycarbonyloxy, alkanesulfonyloxy, arylsulfonyloxy, alkyl

[0244] -carbonyloxy (eg, acetyloxy), arylcarbonyloxy, aryloxy, methoxy, N,O-dimethylhydroxyamino, 9-phenylxanthenyl (pixyl), and haloformates.

[0245] "Pharmaceutically acceptable salts" means salts that are suitable for use in contact with human and lower animal tissues within the scope of reasonable medical judgment, without excessive toxicity, irritation, allergic reaction, etc., and commensurate with a reasonable benefit / risk ratio. Pharmaceutically acceptable salts are well known in the art.

[0246] The term "tautomer" or "tautomeric" refers to two or more interconvertible compounds resulting from tautomerization. The exact ratio of tautomers depends on a number of factors, including, for example, temperature, solvent, and pH. Tautomerism is known to those skilled in the art. Exemplary tautomerism includes keto to enol, amide to imide, lactam to lactim, enamine to imine, and enamine to (a different enamine) tautomerism.

[0247] As used herein, the term "subject" (also referred to herein as "patient") refers to an animal, preferably a mammal, most preferably a human, who is the object of treatment, observation, or experiment.

[0248] As used in this application, the terms "treat", "treating", "treatment" and "treatment" are

[0249] Etc. refer to eliminate, reduce or improve disease or illness and / or symptoms associated therewith. Although not excluded, it is not necessary to completely eliminate the disease, illness or symptom associated therewith for the treatment of disease or illness. As used herein, the terms "treat", "treating", "treatment" etc. may include "preventive treatment", which refers to reducing the disease or illness redevelopment in a subject who is not suffering from but has a risk of illness or is susceptible to disease or illness redevelopment or disease or illness recurrence, or the possibility of previously controlled disease or illness recurrence. The term "treatment" and synonyms relate to giving a compound described in the present application of a therapeutically effective amount to a subject who needs such treatment.

[0250] The term "effective amount" or "therapeutically effective amount" refers to an amount of a compound or combination of compounds as described herein that is sufficient to achieve the intended application, including but not limited to: preventing or treating a disease. The therapeutically effective amount may vary depending on the intended application (in vitro or in vivo), or the subject and the condition being treated (e.g., body weight, age and gender of the subject), the severity of the condition, the mode of administration, etc., which can be easily determined by a person of ordinary skill in the art. The term also applies to a dose that induces a specific response in a response in a target cell and / or tissue. The specific dose will vary depending on the specific compound selected, the dosage regimen to be followed, whether the compound is administered in combination with other compounds, the time of administration, the tissue to which it is administered, and the physical delivery system that carries the compound.

[0251] As used in this application, the singular forms "a," "an," and "the"

[0252] Plural references are included unless expressly stated or it is clear from the context that this is not the case.

[0253] As used herein, the term "and / or" as used in phrases such as "A and / or B" is intended to include A and B; A or B; A (alone); and B (alone). Similarly, the term "and / or" as used in phrases such as "A, B, and / or C" is intended to encompass each of the following embodiments: A, B, and C; A, B, or C; A or C; A or B;

[0254] B or C; A and C; A and B; B and C; A (alone); B (alone); and C (alone).

[0255] The titles and subtitles are for convenience and / or formal compliance only, do not limit the subject technology, and are not associated with the explanation of the description of the subject technology. In various embodiments, the features described under a title or a subtitle of the subject disclosure scheme can be combined with the features described under other titles or subtitles. In addition, all features under a single title or a single subtitle are not necessarily used together in an embodiment.

[0256] Example

[0257] The various parent materials, intermediates and compounds of each embodiment in the application can be separated and purified using conventional techniques in appropriate circumstances, such as precipitation, filtration, crystallization, evaporation, distillation and chromatography. The characterization of these compounds can be carried out using conventional methods, such as by fusing point, mass spectrum, nuclear magnetic resonance and various other spectral analyses. The illustrative embodiments for carrying out the synthetic step of product described in the application are described in more detail below.

[0258] Example 1. (3R)-3-(2-hydroxy-2-(2-(oxazol-2-yl)phenyl)acetoxy)-1,1-dimethylpyrrolidine

[0259] Synthesis of 1-onium trifluoroacetate

[0260]

[0261] Schema 1

[0262]

[0263] Step 1: Add 2-(2-bromophenyl)acetic acid (S-1) (10 g, 0.047 mol) to MeOH (100 mL).

[0264] Concentrated H2SO4 (15.2 mL, 0.28 mol) was added dropwise to the solution. After the addition was complete, the resulting mixture was heated to reflux for 16 hours. The solvent was evaporated to dryness and the residue was poured into ice water (100 mL). The mixture was extracted with EA (50 mL x 2), dried and concentrated to give crude methyl 2-(2-bromophenyl)acetate (S-2). MS (ESI) m / z 229.1.

[0265] Step 2 A mixture of methyl 2-(2-bromophenyl)acetate (S-2) (10 g, crude, 0.0467 mol), NBS (9 g, 0.051 mol) and AIBN (3.83 g, 0.023 mol) in CCl4 (100 mL) was heated at 80° C. under N2 for 16 h. The solvent was removed and the residue was diluted with DCM (150 mL), washed with water and brine, dried over Na2SO4 and concentrated to give methyl 2-bromo-2-(2-bromophenyl)acetate (S-3).

[0266] Step 3 Under N2, a small amount of NaH (2.154 g, 0.054 mol) was added to a solution of 4-methoxyphenol (S-4) (4.45 g, 0.0359 mol) in dry THF (250 mL) at 0°C. The resulting mixture was stirred at 0°C for 30 min, followed by the addition of 2-bromo-2-(2-bromophenyl)acetic acid methyl ester (S-3) (15 g, crude product, 0.047 mol) and TBAI (776 mg, 0.007 mol). The resulting reaction mixture was stirred at room temperature for 16 hours. The reaction was quenched with NH4Cl (100 mL) aqueous solution at 0°C, and then extracted with EA (50 mL x 2). The combined organic phases were concentrated, and the residue was purified by silica gel column chromatography (PE / EA = 95:5 to 90:10) to give 2-(2-bromophenyl)-2-(4-methoxyphenoxy)acetic acid methyl ester (S-5). 1 HNMR (400MHz,

[0267] CDCl3):7.72-7.64(m,2H),7.43-7.38(m,1H),7.29-7.24(m,1H),6.98-6.94(m,2H),

[0268] 6.88-6.84(m,2H),6.10(s,1H),3.81(s,3H),3.79(s,3H).

[0269] Step 4 To a solution of methyl 2-(2-bromophenyl)-2-(4-methoxyphenoxy)acetate (S-5) (1.0 g, 3.13 mmol) in MeOH (10 mL), THF (10 mL) and water (10 mL) was added LiOH (160 mg, 3.8 mmol) and the resulting reaction mixture was stirred at 40° C. for 16 hours. MeOH and THF were removed under vacuum and the residue was diluted with HCl (1 N, 20 mL). Extracted with EA (30 mL×3), dried and concentrated to give 2-(2-bromophenyl)-2-(4-methoxyphenoxy)acetic acid (S-6).

[0270] Step 5 At 0°C, 2-(2-bromophenyl)-2-(4-methoxyphenoxy)acetic acid (S-6) (2.0 g,

[0271] To a solution of (5.931mmol) in dry DCM (20mL) was added (COCl) (0.75mL, 8.897mmol) and DMF (one drop). The mixture was stirred at room temperature for 1 hour. The reaction mixture was then concentrated under vacuum to give 2-(2-bromophenyl)-2-(4-methoxyphenoxy)acetyl chloride (S-7) (2.1g, crude). The crude product was used in the next step without further purification.

[0272] Step 6 To a solution of 2-(2-bromophenyl)-2-(4-methoxyphenoxy)acetyl chloride (S-7) (2.1 g, 5.91 mmol) in dry DCM (20 mL) at 0°C was added (R)-1-methylpyrrolidin-3-ol (S-8) (717 mg, 7.09 mmol) and TEA (1.8 g, 17.73 mmol). The resulting reaction mixture was stirred at room temperature for 2 hours. The reaction was quenched with water (30 mL) and extracted with DCM (30 mL x 3). The combined organic layers were washed with water (40 mL x 3).

[0273] The filtrate was concentrated and the crude product was purified by silica gel column chromatography with MeOH:DCM (0-5%) to give (R)-1-methylpyrrolidin-3-yl 2-(2-bromophenyl)-2-(4-methoxyphenoxy)acetate (S-9). MS (ESI) m / z 422.1 [M+H] + .

[0274] Step 7 2-(2-bromophenyl)-2-(4-methoxyphenoxy)acetic acid-(R)-1-methylpyrrolidin-3-yl ester

[0275] A mixture of (S-9) (509 mg, 1.2 mmol), 2-(tributyltinyl)oxazole (S-10) (862 mg, 2.4 mmol) and Pd(PPh3)4 (277 mg, 0.24 mmol) and dioxane (15 mL) was heated at 100°C under N2 for 16 hours. The solvent was removed and the residue was purified by prep-TLC (DCM / MeOH=10:1) to give (R)-1-methylpyrrolidin-3-yl 2-(4-methoxyphenoxy)-2-(2-(oxazol-2-yl)phenyl)acetate

[0276] (S-11). MS(ESI)m / z 409.4[M+H] + .

[0277] Step 8 To 2-(4-methoxyphenoxy)-2-(2-(oxazol-2-yl)phenyl)acetic acid-(R)-1-methylpyrrolidine

[0278] -3-yl ester (S-11) (80mg, 0.2mmol) in MeCN (15mL) and water (15mL) was added cerium ammonium nitrate (CAN) (550mg, 1.0mmol). The resulting reaction mixture was stirred at room temperature for 20 hours. The solvent was removed in vacuo, and the residue was diluted with H2O and then extracted with EA (15mL x3). The combined organic phase was dried and concentrated. The residue was purified by preparative HPLC to obtain 2-hydroxy-2-(2-(oxazole-2-

[0279] (R)-1-methylpyrrolidin-3-yl (((R)-1-methylpyrrolidin-3-yl)phenyl)acetate (S-12).

[0280] Step 9: (R)-1-methylpyrrolidin-3-yl 2-hydroxy-2-(2-(oxazol-2-yl)phenyl)acetate

[0281] To a solution of (S-12) (9 mg, 0.03 mmol) in 2-butanone (3 mL) was added CH3I (43 mg, 0.3 mol).

[0282] The reaction mixture was placed in a sealed tube and heated at 75°C overnight. The reaction mixture was concentrated and the residue was purified by preparative HPLC to give (3R)-3-(2-hydroxy-2-(2-(oxazol-2-yl)phenyl)acetoxy)-1,1-

[0283] Dimethylpyrrolidin-1-ium trifluoroacetate (Example 1). 1 H NMR (400 MHz, D2O): 7.94-7.90

[0284] (m,2H),7.57-7.51(m,2H),7.42-7.36(m,1H),7.29-7.214(m,1H),6.01-5.95(m,1H),

[0285] 5.42(br,1H),3.76-3.33(m,3H),3.05(s,3H),2.77-2.69(m 3H),2.66-2.51(m,2H),

[0286] 2.17-2.08(m,1H),1.89-1.79(m,1H).MS(ESI)m / z 317.1[M+H] + .

[0287] Example 2 and Example 3. Synthesis of (3R)-3-(2-(2-(cyclopent-1-en-1-yl)phenyl)-2-hydroxyacetoxy)-1,1-dimethylpyrrolidin-1-ium trifluoroacetate

[0288]

[0289] Schema 2

[0290]

[0291] Step 1 In an ice bath, 2-(2-bromophenyl)-2-(4-methoxyphenoxy)acetyl chloride (S-7) (2.1 g,

[0292] To a solution of (R)-1-methylpyrrolidin-3-ol (S-8) (717 mg, 7.09 mmol) in dry DCM (20 mL) was added (R)-1-methylpyrrolidin-3-ol (S-8) (717 mg, 7.09 mmol) and TEA (1.8 g, 17.73 mmol). The mixture was stirred at room temperature for 2 hours. The mixture was quenched with water (30 mL) and extracted with DCM (30 mL x 3). The organic layer was dried over Na2SO4 and filtered. The filtrate was concentrated and purified by silica gel column chromatography eluting with MeOH:DCM (0-5%) to give (R)-1-methylpyrrolidin-3-yl 2-(2-bromophenyl)-2-(4-methoxyphenoxy)acetate (S-13). MS (ESI)

[0293] m / z 422.1[M+H] + .

[0294] Step 2 To a solution of 2-(2-bromophenyl)-2-(4-methoxyphenoxy)acetic acid-(R)-1-methylpyrrolidin-3-yl ester (S-13) (1.57 g, 3.74 mmol) in CH3CN / H2O (30 mL / 6 mL) was added CAN (6.14 g, 11.206 mmol). The mixture was stirred at room temperature overnight. The mixture was quenched with water (30 mL) and extracted with EA (30 mL x 3). The organic layer was washed with HCl (0.5 M, 20 mL x 2). The aqueous layer was basified to pH = 9 with Na2CO3 (aq.). The mixture was extracted with EA (30 mL x 3). The combined organic layers were dried over Na2SO4 and filtered.

[0295] The filtrate was concentrated to give (R)-1-methylpyrrolidin-3-yl 2-(2-bromophenyl)-2-hydroxyacetate (S-14) (600

[0296] mg, crude product), used directly in the next step without further purification. MS (ESI) m / z 316.0 [M+H] + .

[0297] Step 3 A solution of a mixture of 2-(2-bromophenyl)-2-hydroxyacetic acid-(R)-1-methylpyrrolidin-3-yl ester (S-14) (480 mg, 1.529 mmol), cyclopent-1-ene-1-boronic acid (S-15) (257 mg, 2.293 mmol), K3PO4 (972 mg, 4.587 mmol) and Pd(dppf)Cl2 (112 mg, 0.153 mmol) in 1,4-dioxane (15 mL) was heated to 110° C. under nitrogen atmosphere for 16 hours. The mixture was quenched with water (30 mL) and extracted with EA (30 mL x 3). The combined organic layers were dried over Na2SO4 and filtered. The filtrate was concentrated and purified by silica gel column chromatography eluting with MeOH:DCM (0-10%) to give a mixture of diastereoisomers of (R)-1-methylpyrrolidin-3-yl 2-(2-(cyclopent-1-en-1-yl)phenyl)-2-hydroxyacetate. Further separation was performed using an IH column from Daicel using Hex-EtOH (9:1) to give the S-16a fast eluting isomer and the S-16b slow eluting isomer.

[0298] Step 4 To a solution of S-16a (70.0 mg, 0.233 mmol) in 2-butanone (3 mL) was added CH3I (3 drops). The mixture was stirred at 75°C for 4 hours. The mixture was concentrated and then purified by preparative HPLC to give (R)-3-(-2-(2-(cyclopent-1-ene-1-yl)phenyl)-2-hydroxyacetoxy)-1,1-dimethylpyrrolidin-1-ium trifluoroacetate (Example 2). 1 H NMR (400MHz, D2O): δ=7.47-7.39(m,4H),5.89(t,J=2.0Hz,1H),5.71(s,1H),5.57(t,J=6Hz,1H),3.89-3.77(m,2H),3.61-3.48(m,2H),3.20 (s,3H),2.93(s,3H),2.79-2.75(m,1H),2.72-2.68(m,2H),2.58-2.54(m,2H),2.19-2.11(m,1H),2.08-2.00(m,2H).MS(ESI)m / z316.2[M+H] + .

[0299] Example 3 was prepared from S-16b in the same manner as Example 2. 1H NMR (400MHz, D2O): δ=7.46-7.37(m,4H),5.89(t,J=2.0Hz,1H),5.72(s,1H),5.61(br,1H),3.82-3.78(dd,1H),3.71-3.57(m,2H),3.53(d ,1H),3.16(s,3H),2.81-2.75(m,1H),2.76(s,3H),2.73-2.68(m,2H),2.59-2.55(m,2H),2.42-2.34(m,1H),2.05(quint,2H).MS(ESI)m / z 316.2[M+H] + .

[0300] Example 4 and Example 5. Synthesis of (3S)-3-(2-(2-(cyclopent-1-en-1-yl)phenyl)-2-hydroxyacetoxy)-1,1-dimethylpyrrolidin-1-ium trifluoroacetate

[0301]

[0302] Starting from (S)-1-methylpyrrolidin-3-ol, Examples 4 and 5 were synthesized in the same manner as described in Examples 2 and 3; Example 4 was derived from the fast eluting isomer of (S)-1-methylpyrrolidin-3-yl 2-(2-(cyclopent-1-en-1-yl)phenyl)-2-hydroxyacetate, and Example 5 was derived from the corresponding slow eluting isomer. 1 H NMR appears identical to Example 3. 1 H NMR appeared identical to Example 2.

[0303] Example 6 and Example 7. Synthesis of (R)-2-((2-(2-(cyclopent-1-en-1-yl)phenyl)-2-hydroxyacetoxy)methyl)-1,1-dimethylpyrrolidin-1-ium trifluoroacetate

[0304]

[0305] Diagram 3

[0306]

[0307] Step 1 To a solution of (R)-(1-methylpyrrolidin-2-yl)methanol (0.68 g, 5.9 mmol) and TEA (1.19 g, 11.8 mmol) in DCM (20 mL) was added 2-(2-bromophenyl)-2-(4-methoxyphenoxy)acetyl chloride (S-7) (2.1 g, 5.9 mmol) in DCM (10 mL) at 0°C over 20 minutes, and the resulting reaction mixture was stirred at 45°C for 2 h. The mixture was quenched with H2O and then extracted with DCM. The combined organic phases were dried over Na2SO4 and concentrated to give the crude product. The crude product was purified by silica gel column chromatography (PE / EA

[0308] =1 / 1) to give ((R)-1-methylpyrrolidin-2-yl)methyl 2-(2-bromophenyl)-2-(4-methoxyphenoxy)acetate (S-17). MS (ESI) m / z 433.9 [M+H] + .

[0309] Step 2: To a solution of ((R)-1-methylpyrrolidin-2-yl)methyl 2-(2-bromophenyl)-2-(4-methoxyphenoxy)acetate (S-17) (2.1 g, 4.9 mmol) in CH3CN / H2O (10 mL / 10 mL) was added CAN

[0310] (8.0 g, 14.6 mmol). The resulting reaction mixture was stirred at room temperature overnight. The mixture was concentrated, the residue was diluted with water (50 mL), and extracted with EA (50 mL). The aqueous phase was adjusted to pH 5 with Na2CO3 solution.

[0311] =9. The resulting mixture was extracted with EA (100 mL x 2). The combined organic phase was washed with brine, dried over Na2SO4, and concentrated to give crude 2-(2-bromophenyl)-2-hydroxyacetic acid ((R)-1-methylpyrrolidin-2-yl)methyl ester (S-18)

[0312] (0.9 g, yield: 56.6%), the product was used directly in the next step without further purification. MS (ESI) m / z 327.9

[0313] [M+H] + .

[0314] Step 3 2-(2-bromophenyl)-2-hydroxyacetic acid ((R)-1-methylpyrrolidin-2-yl)methyl ester (S-18) (0.8

[0315] g, 2.4 mmol), cyclopent-1-en-1-ylboronic acid (S-15) (0.4 g, 3.6 mmol), K3PO4 (1.01 g,

[0316] A mixture of 2-(2-(cyclopent-1-ene-1-yl)phenyl)-2-hydroxyacetic acid-((R)-1-methylpyrrolidine-2-yl)-1-yl)-1-nitropropene (2-nitropropene-1-yl)-1-nitropropene (2-nitropropene-2-yl)-1-nitropropene (2-nitropropene-1-yl)-1-nitropropene (2-nitropropene-2-yl)-1-nitropropene (2-nitropropene-1-yl)-1-nitropropene (2-nitropropene-2-yl)-1-nitropropene (2-nitropropene-1-yl)-1-nitropropene (2-nitropropene-2-yl)-1-nitropropene (2-nitropropene-1-yl)-1-nitropropene

[0317] The fast isomer S-19a and the slow isomer S-19b were obtained by further separation on a chiral column IH from Daicel, eluting with hexane:EtOH (9:1, containing 0.3% DEA).

[0318] Step 4: To a solution of S-19a (30 mg, 0.095 mmol) in 2-butanone (1 mL) was added CH3I

[0319] (1 mL). The resulting reaction mixture was loaded into a sealed tube and stirred at 65° C. for 2 h. The mixture was concentrated and purified by preparative HPLC (0.1% TFA as an additive) to afford Example 6, one enantiomer of (R)-2-((2-(2-(cyclopent-1-en-1-yl)phenyl)-2-hydroxyacetoxy)methyl)-1,1-dimethylpyrrolidin-1-ium trifluoroacetate. 1 H NMR(400MHz,D2O):7.36-7.26(m,4H)5.79-5.78(t,J=2.2Hz,

[0320] 1H),5.63(s,1H),4.68-4.64(m,1H),4.28-4.22(m,1H),3.74-3.67(m,1H),3.36-3.28

[0321] (m,2H),2.70(s,3H),2.67(s,3H),2.64-2.58(m,2H),2.51-2.44(m,2H),2.26-2.20(m,

[0322] 1H),2.07-1.82(m,5H).MS(ESI)m / z 330.2[M+H] + .

[0323] Example 7 was prepared from S-19b, 1H NMR (400MHz, D2O): 7.38-7.31(m,4H)5.80-5.79(t,J=2.0Hz,1H),5.65(s,1H),4.50-4.38(m,2H),3.85-3.81(m,1H),3.41-3.37 (m,2H),2.69(s,3H),2.63-2.58(m,5H),2.51-2.46(m,2H),2.24-2.22(m,1H),2.04-1.83(m,4H),1.71-1.66(m,1H).MS(ESI)m / z 330.2[M+H] + .

[0324] Example 8 and Example 9. Synthesis of (S)-2-((2-(2-(cyclopent-1-en-1-yl)phenyl)-2-hydroxyacetoxy)methyl)-1,1-dimethylpyrrolidin-1-ium trifluoroacetate

[0325]

[0326] Examples 8 and 9 were synthesized starting from (S)-(1-methylpyrrolidin-2-yl)methanol in the same manner as described in Examples 6 and 7, with Example 8 being derived from the faster eluting isomer of (S)-1-methylpyrrolidin-2-yl)methyl 2-(2-(cyclopent-1-en-1-yl)phenyl)-2-hydroxyacetate and Example 9 being derived from the corresponding slower eluting isomer. 1 H NMR appears identical to Example 6. 1 H NMR appeared identical to Example 7.

[0327] Example 10. Synthesis of 3-[2-(2-cyclopentylphenyl)-2-hydroxy-acetoxy]-1,1-dimethylpyrrolium chloride

[0328]

[0329] Schema 4

[0330]

[0331] Step 1 To a solution of 1-methylpyrrolidin-3-ol (300 mg, 2.97 mmol) and TEA (400 mg, 3.95 mmol) in DCM (15 mL) was added 2-(2-bromophenyl)-2-(4-methoxyphenoxy)acetyl chloride (S-7) (710 mg, 1.98 mmol) at 0°C over 10 minutes. The mixture was stirred at room temperature for 2 hours. The mixture was quenched with H2O and extracted with DCM. The combined organic phases were dried over Na2SO4 and concentrated to give the crude product. The crude product was purified by silica gel column chromatography (PE / EA=1 / 1) to give 2-(2-bromophenyl)-2-(4-methoxyphenoxy)acetic acid-1-methylpyrrolidin-3-yl ester (S-20). MS (ESI) m / z 422.1 [M+H] + .

[0332] Step 2: 2-(2-bromophenyl)-2-(4-methoxyphenoxy)acetic acid-1-methylpyrrolidin-3-yl ester (S-20)

[0333] Cyclopent-1-en-1-ylboronic acid (S-5) (491 mg, 2.53 mmol), K2CO3 (699 mg, 5.07 mmol) and Pd(dppf)Cl2 were added to a solution of cyclopent-1-en-1-ylboronic acid (S-5) (491 mg, 2.53 mmol), K2CO3 (699 mg, 5.07 mmol) and Pd(dppf)Cl2

[0334] (123 mg, 0.169 mmol). The resulting mixture was degassed and filled with N2. The reaction mixture was then heated at 110°

[0335] C. and stirred overnight. The reaction mixture was diluted with water (20 mL) and extracted with EA (50 mL). The organic phase was washed with brine, dried over Na2SO4, and then concentrated. The residue was purified by silica gel column chromatography (DCM / MeOH

[0336] =20 / 1) to obtain (2-cyclopent-1-enylphenyl)-(4-methoxyphenoxy)acetic acid-1-methylpyrrolidin-3-yl ester (S-21). MS (ESI) m / z 408.2 [M+H] + .

[0337] Step 3: (2-cyclopent-1-enylphenyl)-(4-methoxyphenoxy)acetic acid-1-methylpyrrolidine

[0338] -3-yl ester (S-21) (330 mg, 0.81 mmol) in 2-butanone (5 mL) was added K2CO3 (20 mg, 0.081 mmol) and CH3I (571 mg, 4.05 mmol). The resulting reaction mixture was loaded into a sealed tube and stirred at 75 ° C overnight. The mixture was concentrated and purified by preparative HPLC to give 3-[2-(2-cyclopent-1-enylphenyl)-2-(4-methoxyphenoxy)acetoxy]-1,1-dimethylpyrrolidinium trifluoroacetate (S-22). MS (ESI) m / z 422.3 [M] + .

[0339] Step 4: 3-[2-(2-cyclopent-1-enyl-phenyl)-2-(4-methoxyphenoxy)-acetoxy]-1,1-

[0340] Dimethylpyrrolidine trifluoroacetate (S-22) (81 mg, 0.189 mmol) and Pd / C (~20 mg, 20%

[0341] The mixture was then degassed at room temperature for 16 hours. The reaction mixture was filtered through celite and concentrated to give the crude product 3-[2-(2-(2-pentylphenyl)-4-(1-methoxyphenoxy)-acetoxy]-1,1-dimethylpyrrolidine trifluoroacetate (S-23), which was used directly in the next step.

[0342] MS (ESI) m / z 424.3 [M] + .

[0343] Step 5: At room temperature, add the crude 3-[2-(2-cyclopentylphenyl)-2-(4-methoxyphenoxy)-

[0344] [acetoxy]-1,1-dimethylpyrrolidine trifluoroacetate (S-23) (80 mg, 0.189 mmol) and CH3CN / H2O

[0345] CAN (625 mg, 1.14 mmol) was added to the mixture of (5 mL / 5 mL). The resulting reaction mixture was stirred at room temperature overnight. The mixture was concentrated, the residue was diluted with water (10 mL) and washed with EA (10 mL x 2).

[0346] Extraction. The aqueous phase was adjusted to pH=9 using Na2CO3 solution and extracted again with EA (10 mL x 2). The combined organic phases were dried and concentrated using Na2SO4. The residue was purified by preparative HPLC (0.1% TFA as an additive), and the product was treated with a few drops of HCl and lyophilized to give 3-[2-(2-cyclopentyl-phenyl)-2-hydroxy-acetoxy]-1,1-dimethyl-pyrrolium chloride (Example 10). 1 H NMR (400 MHz, D2O, mixture of two diastereomers): 7.44-7.42 (m, 2H, two diastereomers), 7.36-7.33 (m, 2H, two diastereomers), 7.27-7.20 (m, 2H, two diastereomers), 5.72 (s, 1H, enantiomers

[0347] 1), 5.70 (s, 1H, enantiomer 2), 5.54 (br, 2H, two diastereomers), 3.81-3.68 (m, 3H, two diastereomers), 3.63-3.41 (m, 5H, two diastereomers), 3.12 (s, 3H, diastereomer 1), 3.08 (3, 3H, diastereomer 2), 2.86 (s, 3H, diastereomer 1), 2.73-2.64 (m, 5H, two diastereomers), 2.32-2.29 (m, 1H, diastereomer 1), 2.08-1.92 (m, 5H, two diastereomers

[0348] enantiomers), 1.77-1.51 (m, 12H, two diastereomers). MS (ESI) m / z 318.2 [M] + Example 11. Synthesis of 3-(2-([1,1'-biphenyl]-2-yl)-2-hydroxyacetoxy)-1,1-dimethylpyrrolidin-1-ium chloride

[0349]

[0350] Diagram 5

[0351]

[0352] Step 1: 2-(2-bromophenyl)-2-(4-methoxyphenoxy)acetic acid methyl ester (S-5) (1.06 g, 3.02

[0353] mmol), phenylboronic acid (553 mg, 4.53 mmol), KOAc (444 mg, 4.53 mmol) and Pd(PPh3)4

[0354] A mixture of 4-(175 mg, 0.15 mmol) and CH3CN / H2O (75 mL / 16 mL) was degassed and filled with N2. The resulting mixture was then heated at 80°C overnight. The reaction mixture was concentrated and the residue was purified by silica gel column chromatography (PE / EA=10 / 1) to give methyl 2-([1,1'-biphenyl]-2-yl)-2-(4-methoxyphenoxy)acetate (S-24).

[0355] MS (ESI) m / z 366.2 [M+18] +

[0356] Step 2: methyl 2-([1,1'-biphenyl]-2-yl)-2-(4-methoxyphenoxy)acetate (S-24) (908

[0357] mg, 2.6 mmol) in MeOH / THF / H2O solution (10 mL / 10 mL / 10 mL) was added with LiOH·H2O

[0358] (131 mg, 3.12 mmol). The resulting mixture was stirred at 40° C. overnight. The reaction mixture was concentrated.

[0359] The residue was diluted with water (10 mL), acidified with dilute HCl until pH reached 2 and extracted with EA (20 mL x 3). The combined organic phases were washed with brine (20 mL), dried over Na2SO4 and concentrated to give 2-([1,1'-biphenyl]-2-yl)-2-(4-methoxyphenoxy)acetic acid. MS (ESI) m / z 333.2 [MH] - .

[0360] Step 3: At 0°C, 2-([1,1'-biphenyl]-2-yl)-2-(4-methoxyphenoxy)acetic acid (890

[0361] mg, 2.6 mmol) and DCM (15 mL) were added dropwise with DMF (one drop) and oxalyl chloride (500 mg, 3.9 mmol). The mixture was stirred at room temperature for 2 hours. The mixture was then concentrated to give biphenyl-2-yl-

[0362] (4-Methoxyphenoxy)-acetyl chloride (S-25) was used directly in the next step.

[0363] Step 4: A solution of 2-([1,1'-biphenyl]-2-yl)-2-(4-methoxyphenoxy)acetyl chloride (S-25) (900 mg, 2.60 mmol) in DCM (10 mL) was added dropwise to a mixture of 1-methylpyrrolidin-3-ol (240 mg, 2.36 mmol) and TEA (290 mg, 2.83 mmol) and DCM (20 mL) at 0 ° C for 20 minutes. After the addition, the mixture was stirred for 2 hours and the temperature was slowly warmed to room temperature. LCMS showed that the reaction was complete. The mixture was quenched with water and extracted with DCM (30 mLx3). The combined organic phase was dried with Na2SO4 and concentrated. The residue was purified by silica gel column chromatography (DCM / MeOH=20 / 1) to give 2-([1,1'-biphenyl]-2-yl)-2-(4-methoxyphenoxy)acetic acid-1-methylpyrrolidin-3-yl ester (S-26). MS (ESI) m / z 418.2 [M+H] + .

[0364] Step 5 A sealed tube was charged with a solution of 2-([1,1'-biphenyl]-2-yl)-2-(4-methoxyphenoxy)acetic acid-1-methylpyrrolidin-3-yl ester (S-26) (840 mg, 1.85 mmol) and MeI (1.15 mL, 18.5 mmol) in 2-butanone (10 mL), sealed and heated at 75°C for 16 hours. The cooled reaction mixture was concentrated and the residue was purified by preparative HPLC (0.1% TFA as an additive), and the product fraction was treated with HCl and lyophilized to give 3-(2-([1,1'-biphenyl]-2-yl)-2-hydroxyacetoxy)-1,1-dimethylpyrrolidin-1-ium chloride (S-27) as a yellow oil. MS (ESI) m / z 432.2 [M] + .

[0365] Step 6 To a solution of 3-[2-biphenyl-2-yl-2-(4-methoxyphenoxy)-acetoxy]-1,1-dimethylpyrrolidine trifluoroacetate (S-27) (314 mg, 0.73 mmol) in CH3CN / H2O (10 mL / 10 mL) was added CAN (800 mg, 1.46 mmol). The mixture was stirred overnight at room temperature. The mixture was concentrated and the residue was purified by preparative HPLC (0.1% TFA as an additive) to give 3-(2-biphenyl-2-yl-2-hydroxy-acetoxy)-1,1-dimethylpyrrolidine trifluoroacetate (Example 11). 1H NMR(400MHz,D2O):7.50-7.39(m,6H),7.38-7.35(m,3H),5.41(s,1H),5.36(br,1H),3.73-3.66(m,1H),3 .60-3.41(m,3H),3.23-3.12(m,3H),2.83-2.72(m,3H),2.64-2.56(m,1H),2.20-1.98(m,1H).MS(ESI)m / z 326.2[M] + .

[0366] Example 12. Synthesis of 3-(2-hydroxy-2-(2-isopropylphenyl)acetoxy)-1,1-dimethylpyrrolidin-1-ium chloride

[0367]

[0368] Diagram 6

[0369]

[0370] Step 1: 2-(2-bromophenyl)-2-(4-methoxyphenoxy)acetic acid-1-methylpyrrolidin-3-yl ester

[0371] A mixture of (S-20) (500 mg, 1.19 mmol), 4,4,5,5-tetramethyl-2-(prop-1-en-2-yl)-1,3,2-dioxaborolane (240 mg, 1.43 mmol), K2CO3 (328 mg, 2.38 mmol) and Pd(PPh3)4 (137 mg, 0.12 mmol) and dioxane / H2O (10 mL / 1 mL) was stirred overnight at 100 °C under N2. The reaction mixture was diluted with water (20 mL) and extracted with EA (20 mL x 2). The combined organic phases were washed with brine, dried over Na2SO4 and filtered. The filtrate was concentrated and purified by silica gel column chromatography eluting with EA to give 2-(4-methoxyphenoxy)-2-(2-(prop-1-en-2-yl)phenyl)acetic acid-1-methylpyrrolidin-3-yl ester (S-28).

[0372] MS (ESI) m / z 382.2 [M+H] +.

[0373] Step 2 To a solution of 2-(4-methoxyphenoxy)-2-(2-(prop-1-en-2-yl)phenyl)acetate-1-methylpyrrolidin-3-yl ester (S-28) (300 mg, 0.78 mmol) in MeOH (5 mL) was added Pd / C (80 mg). The mixture was then stirred at room temperature under H2 for 4 hours. The reaction mixture was filtered and the filtrate was concentrated to give 2-(2-isopropylphenyl)-2-(4-methoxyphenoxy)acetate-1-methylpyrrolidin-3-yl ester (S-29). MS (ESI) m / z

[0374] 384.2[M+H] + .

[0375] Step 3 To a solution of 2-(2-isopropylphenyl)-2-(4-methoxyphenoxy)acetic acid-1-methylpyrrolidin-3-yl ester (S-29) (270 mg, 0.71 mmol) in CH3CN / H2O (5 mL / 5 mL) was added CAN (1.16 g, 2.11 mmol). The reaction mixture was stirred at room temperature overnight. The reaction mixture was concentrated. The residue was then diluted with water (10 mL) and extracted with EA (20 mL). The aqueous phase was adjusted to 4% by weight using Na2CO3 solution.

[0376] pH = 9. The resulting mixture was extracted with EA (20 mL x 2). The combined organic phases were washed with brine, dried over Na2SO4, and filtered. The filtrate was concentrated to give 2-hydroxy-2-(2-isopropylphenyl)acetic acid-1-methylpyrrolidin-3-yl ester (S-30) as a brown solid, which was used in the next step without further purification. MS (ESI) m / z 278.2 [M+H] + .

[0377] Step 4 To a solution of 2-hydroxy-2-(2-isopropylphenyl)acetate-1-methylpyrrolidin-3-yl ester (S-30) (100 mg, 0.29 mmol) in 2-butanone (2 mL) was added CH3I (1 mL). The mixture was stirred at 65 °C for 2 h. The reaction mixture was concentrated to give a crude product. The crude product was then purified by preparative HPLC (0.1% TFA as an additive), treated with HCl and lyophilized to give 3-(2-hydroxy-2-(2-isopropylphenyl)acetoxy)-1,1-dimethylpyrrolidin-1-ium chloride, Example 12. 1H NMR(400MHz,D2O):7.44(d,J=8Hz,1H),7.40-7.35(m,1H),7.27-7.22(m,2 H),5.71(d,J=9.2Hz,1H),5.54(br,1H),3.83-3.71(m,2H),3.64-3.45(m,2 H),3.31-3.21(m,1H),3.13,3.08(s,3H),2.90,2.73(s,3H),2.71-2.66(m ,1H),2.34-2.30(m,1H),2.13-2.06(m,1H),1.24-1.13(m,6H).MS(ESI)m / z 292.2[M] + .

[0378] Biological Example 1 In vitro assay to determine IC50

[0379] The FLIPR assay was used to evaluate the potency of the compounds. CHO-K1 cells stably expressing the M3 receptor were cultured in culture medium (90% Ham's F-12 nutrient mixture, Gibco; 10% fetal bovine serum, Biosera; 200 μg / mL hygromycin and penicillin (100 U / mL) / streptomycin (100 g / mL, Invitrogen) at 37°C until 100% confluence was reached in a cell culture incubator (ThermoFisher, 5% CO2). Cells were harvested using 0.25% trypsin / EDTA, pelleted by centrifugation at 300 × g for 5 min, and lysed at 5 × 10 5Cells were resuspended in culture medium at a cell density of 10 cells / mL. 20 microliters of cell suspension (10,000 cells / well) were transferred to 384-well plates and cultured for 24 hours before the assay. DMSO was used as a blank control, and scopolamine (MedChemExpress) was used as a positive control for antagonists. Compounds were prepared in DMSO (stock concentration: 1 mM) and diluted 3× (10 concentrations) in 384-LDV plates (Labcyte). 90 nL of the serially diluted compounds were transferred from the 384-LDV plates to the compound plates (PerkinElmer) by Echo 550 (Labcyte), and then 30 uL of assay buffer (1 HBSS containing 20 mM HEPES, pH 7.4, Sigma) was added to each well. For the FLIPR assay, the medium was removed and 20uL of 1x loading dye (assay buffer containing 2μM Fluo-8 AM, AAT Bioquest; 1mM probenecid and 0.0025% pluronic F-127, Sigma) was added to each well. The well plate was incubated at 37°C for 1 hour (protected from light). For the FLIPR assay, the excitation wavelength was set to 470 / 495nm and the emission wavelength was set to 515 / 575nm (Molecular Devices). The assay was performed in agonist and antagonist modes. For the agonist mode, 10μL of diluted compounds were transferred to the cell culture wells and incubated at room temperature for 10 minutes. For the antagonist mode, 10μL of compounds diluted with 8nM acetylcholine (EC80, MedChemExpress) were added to each well and incubated at room temperature for 10 minutes. RFU values ​​were calculated by subtracting the minimum value from the maximum value of the FLIPR signal. The inhibitory effect of the compound on acetylcholine-induced calcium flux was calculated by the following formula: % effect = (RFU 样品 –RFU DMSO ) / (RFU 东莨菪碱 –RFU DMSO )×100. The dose response curve fitting and IC50 values ​​of each compound were calculated by using XLFit. The following table lists the IC50, where * indicates IC50>1000nM; **10-100nM; <10nM.

[0380] Compound IC50 Example 1 ** Example 2 *** Example 3 ** Example 4 ** Example 5 ** Example 6 *** Example 7 ** Example 8 ** Example 9 *** Example 10 ** Embodiment 11 ** Example 12 *

[0381] The Summary and Abstract sections may set forth one or more but not all exemplary embodiments of the present invention as contemplated by the inventor(s), and thus, are not intended to limit the present invention and the appended claims in any way.

[0382] The present invention has been described above with the aid of functional building blocks, which illustrate the implementation of specified functions and their relationships. For ease of description, the application has arbitrarily defined the boundaries of these functional building blocks. Alternative boundaries may be defined as long as the specified functions and their relationships are properly performed.

[0383] For aspects of the invention described as being generic, all individual species are considered individually as independent aspects of the invention. If aspects of the invention are described as "comprising" a feature, embodiments are also contemplated as "consisting of" or "consisting essentially of" the feature.

[0384] The foregoing description of specific embodiments will fully reveal the general nature of the present invention, so that other people, without departing from the general concept of the present invention, can easily modify and / or adapt to the various applications of such specific embodiments by applying knowledge within the technical scope of the art, without excessive experimentation. Therefore, based on the teaching and guidance presented in this application, such adaptations and modifications are intended to fall within the meaning and scope of the equivalents of the disclosed embodiments. It should be understood that the terms or terms of the present application are for the purpose of description rather than limitation, so that the terms or terms of this specification will be interpreted by those skilled in the art according to teaching and guidance.

[0385] The breadth and scope of the present invention should not be limited by any of the above-described exemplary embodiments.

[0386] All of the various aspects, embodiments and options described in this application can be combined in any and all variations.

[0387] All publications, patents, and patent applications mentioned in this patent specification are incorporated herein by reference to the same extent as if each individual publication, patent, or patent application was specifically and individually indicated to be incorporated by reference. If any meaning or definition of a term in this document conflicts with any meaning or definition of the same term in a document incorporated by reference, the meaning or definition assigned to that term in this document shall govern.

Claims

1. A salt having the general formula I: in: X - is the counter ion; R 1 is hydrogen or optionally substituted C 3-8 Carbocyclic group; L 1 Empty, C 1-4 Alkylene, or C 1-4 heteroalkylene; R 2 C 3-6 Cycloalkyl, C 4-7 cycloalkenyl, phenyl, 5-membered heteroaryl having 1-3 ring heteroatoms independently selected from N, O and S, or 6-membered heteroaryl having 1-2 ring heteroatoms independently selected from N, O and S; When R 2 C 3-6 When cycloalkyl is present, it is optionally substituted by one or more independently selected from F, OH, R A OR A Substituents, where R A Each occurrence is independently C 1-4 Alkyl or C 3-6 Cycloalkyl, C 1-4 Alkyl or C 3-6 The cycloalkyl group is optionally substituted by one or more independently selected from F, OH, C 1-4 Alkyl, fluorine-substituted C 1-4 Alkyl, C 1-4 Alkoxy and fluorine substituted C 1-4 Substitution of alkoxy groups; When R 2 C 4-7 When cycloalkenyl is substituted, it is optionally substituted by one or more independently selected from F, OH, R A OR A Substituents, where R A C independently at each occurrence 1-4 Alkyl or C 3-6 Cycloalkyl, C 1-4 Alkyl or C 3-6 The cycloalkyl group is optionally substituted by one or more independently selected from F, OH, C 1-4 Alkyl, fluorine-substituted C 1-4 Alkyl, C 1-4 Alkoxy and fluorine substituted C 1-4 Substitution of alkoxy groups; When R 2 When phenyl is present, it is optionally substituted by one or more independently selected from F, Cl, OH, C 1-4 Alkyl, fluorine-substituted C 1-4 Alkyl, C 1-4 Alkoxy and fluorine substituted C 1-4 Substitution of alkoxy groups; When R 2 When it is a 5-membered heteroaryl group having 1-3 ring heteroatoms independently selected from N, O and S, it is optionally substituted by one or more independently selected from F, Cl, OH, C 1-4 Alkyl, fluorine-substituted C 1-4 Alkyl, C 1-4 Alkoxy and fluorine substituted C 1-4 Substitution of alkoxy groups; When R 2 When it is a 6-membered heteroaryl group having 1-2 ring heteroatoms independently selected from N, O and S, it is optionally substituted by one or more independently selected from F, Cl, OH, C 1-4 Alkyl, fluorine-substituted C 1-4 Alkyl, C 1-4 Alkoxy and fluorine substituted C 1-4 Substitution of alkoxy groups; R 3 and R 4 are independently hydrogen or C 1-6 Alkyl; and j is 1 or 2.

2. The salt according to claim 1, characterized in that: When the R 2 When oxazolyl or thiazolyl, it is optionally substituted by one or more independently selected from F, Cl, OH, C 1-4 Alkyl, fluorine-substituted C 1-4 Alkyl, C 1-4 Alkoxy and fluorine substituted C 1-4 The substituents of the alkoxy group are substituted.

3. The salt according to claim 1, characterized in that: When R 2 When pyridyl or pyrimidinyl, it is optionally substituted by one or more independently selected from F, Cl, OH, C 1-4 Alkyl, fluorine-substituted C 1-4 Alkyl, C 1-4 Alkoxy and fluorine substituted C 1-4 The substituents of the alkoxy group are substituted.

4. The salt according to claim 1, which has the general formula shown in Formula I-1:

5. The salt according to claim 1, which has the general formula shown in general formula I-2:

6. The salt according to any one of claims 1 to 5, wherein L 1 Is empty.

7. The salt according to any one of claims 1 to 5, wherein L 1 C 1-4 Alkylene.

8. The salt according to any one of claims 1 to 5, wherein L 1 For CH2.

9. The salt according to any one of claims 1 to 5, wherein R 1 For hydrogen.

10. The salt according to any one of claims 1 to 5, wherein R 1 It is cyclopentyl.

11. The salt according to any one of claims 1 to 5, wherein R 3 It is methyl.

12. The salt according to any one of claims 1 to 5, wherein R 4 It is methyl.

13. The salt according to any one of claims 1 to 5, wherein j is 1.

14. The salt according to any one of claims 1 to 5, wherein X - It is a pharmaceutically acceptable counter ion.

15. A salt selected from the following structures: in, X - It is a pharmaceutically acceptable counter ion.

16. A salt selected from the following structures: in, X - It is a pharmaceutically acceptable counter ion.

17. A pharmaceutical composition comprising the salt according to any one of claims 14 to 16 and optionally a pharmaceutically acceptable carrier.

18. The pharmaceutical composition according to claim 17, wherein the pharmaceutically acceptable carrier is a topically acceptable carrier.

19. The pharmaceutical composition of claim 17, formulated for topical administration.

20. The pharmaceutical composition of claim 17 in the form of a topical solution, cream, ointment, gel or powder.

21. A compound having the general formula II or a salt thereof: in: R 1 is hydrogen or optionally substituted C 3-8 Carbocyclic group; L 1 Empty, C 1-4 Alkylene, or C 1-4 heteroalkylene; R 2 C 3-6 Cycloalkyl, C 4-7 cycloalkenyl, phenyl, 5-membered heteroaryl having 1-3 ring heteroatoms independently selected from N, O and S, or 6-membered heteroaryl having 1-2 ring heteroatoms independently selected from N, O and S; When R 2 C 3-6 When cycloalkyl is present, it is optionally substituted by one or more independently selected from F, OH, R A OR A Substituents, where R A Each occurrence is independently C 1-4 Alkyl or C 3-6 Cycloalkyl, C 1-4 Alkyl or C 3-6 The cycloalkyl group is optionally substituted by one or more independently selected from F, OH, C 1-4 Alkyl, fluorine-substituted C 1-4 Alkyl, C 1-4 Alkoxy and fluorine substituted C 1-4 Substitution of alkoxy groups; When R 2 C 4-7 When cycloalkenyl is substituted, it is optionally substituted by one or more independently selected from F, OH, R A OR A Substituents, where R A C independently at each occurrence 1-4 Alkyl or C 3-6 Cycloalkyl, C 1-4 Alkyl or C 3-6 The cycloalkyl group is optionally substituted by one or more independently selected from F, OH, C 1-4 Alkyl, fluorine-substituted C 1-4 Alkyl, C 1-4 Alkoxy and fluorine substituted C 1-4 Substitution of alkoxy groups; When R 2 When phenyl is present, it is optionally substituted by one or more independently selected from F, Cl, OH, C 1-4 Alkyl, fluorine-substituted C 1-4 Alkyl, C 1-4 Alkoxy and fluorine substituted C 1-4 Substitution of alkoxy groups; When R 2 When it is a 5-membered heteroaryl group having 1-3 ring heteroatoms independently selected from N, O and S, it is optionally substituted by one or more independently selected from F, Cl, OH, C 1-4 Alkyl, fluorine-substituted C 1-4 Alkyl, C 1-4 Alkoxy and fluorine substituted C 1-4 Substitution of alkoxy groups; When R 2 When it is a 6-membered heteroaryl group having 1-2 ring heteroatoms independently selected from N, O and S, it is optionally substituted by one or more independently selected from F, Cl, OH, C 1-4 Alkyl, fluorine-substituted C 1-4 Alkyl, C 1-4 Alkoxy and fluorine substituted C 1-4 Substitution of alkoxy groups; R 3 is hydrogen or C 1-6 Alkyl; and j is 1 or 2.

22. The compound or salt thereof according to claim 21, characterized in that: When the R 2 When oxazolyl or thiazolyl, it is optionally substituted by one or more independently selected from F, Cl, OH, C 1-4 Alkyl, fluorine-substituted C 1-4 Alkyl, C 1-4 Alkoxy and fluorine substituted C 1-4 The substituents of the alkoxy group are substituted.

23. The compound or salt thereof according to claim 21, characterized in that: When the R 2 When pyridyl or pyrimidinyl, it is optionally substituted by one or more independently selected from F, Cl, OH, C 1-4 Alkyl, fluorine-substituted C 1-4 Alkyl, C 1-4 Alkoxy and fluorine substituted C 1-4 The substituents of the alkoxy group are substituted.

24. The compound or salt thereof according to claim 21, which has the general formula according to Formula II-1:

25. The compound or salt thereof according to claim 21, which has the general formula shown in Formula II-2:

26. The compound or salt thereof according to any one of claims 21 to 25, wherein L 1 Is empty.

27. The compound or salt thereof according to any one of claims 21 to 25, wherein L 1 C 1-4 Alkylene.

28. The compound or salt thereof according to any one of claims 21 to 25, wherein L 1 For CH2.

29. The compound or salt thereof according to any one of claims 21 to 25, wherein R 1 For hydrogen.

30. The compound or salt thereof according to any one of claims 21 to 25, wherein R 1 It is cyclopentyl.

31. The compound or salt thereof according to any one of claims 21 to 25, wherein R 3 It is methyl.

32. The compound or salt thereof according to any one of claims 21 to 25, wherein j is 1.

33. A pharmaceutically acceptable salt of the compound of any one of claims 21-32.

34. A pharmaceutical composition comprising the pharmaceutically acceptable salt of claim 33 and optionally a pharmaceutically acceptable carrier.

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