IP Library Granted Patent US 7,238,709
Granted Patent B2
US 7,238,709 · App. 09/732,241 · Granted Jul 3, 2007

Therapeutic carbamates

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Quick Facts
Patent No.
US 7,238,709
App. No.
09/732,241
Granted
Jul 3, 2007
Kind
B2
Abstract

This invention relates to hindered carbamate derivatives that are muscarinic receptor antagonists, pharmaceutical compositions comprising such compounds, and methods of preparing these compounds.

Claims (44)

1. A compound of the formula:

wherein:

A is phenyl;

B″ is —O—;

R X is alkyl, alkenyl, or alkynyl, each optionally substituted with 1 to 5 alkoxy or fluoro substituents;

R 1 is hydrogen or alkyl;

R 2 is phenyl;

K is a bond;

K″ is a bond; and

B is a piperidine ring;

R 46 is alkyl, substituted alkyl, cycloalkyl, substituted cycloalkyl, or heterocycle;

R 47 is alkyl, substituted alkyl, aryl, acyl, heterocycle, or —COOR 50 where R 50 is alkyl; or

R 46 and R 47 together with the nitrogen atom to which they are attached form a heterocycle, which hetorocycle is optionally substituted with one or more alkyl, substituted alkyl, alkenyl, substituted alkenyl, alkynyl, substituted alkynyl, alkoxy, substituted alkoxy, cycloalkyl, substituted cycloalkyl, cycloalkenyl, substituted cycloalkenyl, acyl, acylamino, acyloxy, amino, substituted amino, aminoacyl, aminoacyloxy, oxyaminoacyl, azido, cyano, halo, hydroxyl, keto, thioketo, carboxyl, carboxyalkyl, thioaryloxy, thioheteroaryloxy, thioheterocyclooxy, thiol, thioalkoxy, substituted thioalkoxy, aryl, aryloxy, heteroaryl, heteroaryloxy, heterocycle, heterocyclooxy, hydroxyamino, alkoxyamino, nitro, —SO-alkyl, —SO-substituted alkyl, —SO-aryl, —SO-heteroaryl, —SO 2 -alkyl, -SO 2 -substituted alkyl, —SO 2 -aryl or —SO 2 -heteroaryl;

X is alkylene optionally substituted with one, two, or three hydroxy groups, alkylene wherein one, two, or three carbon atoms have been replaced by an oxygen atom, or an -alkylene-phenylene-alkylene- wherein the phenylene ring is optionally substituted with one or two chloro or fluoro groups;

or a pharmaceutically acceptable salt thereof.

2. The compound of claim 1 wherein R 1 is hydrogen, methyl, or ethyl.

3. The compound of claim 1 wherein R X is (C 1 -C 6 )alkyl, (C 2 -C 6 )alkenyl, (C 2 -C 6 )alkynyl, each optionally substituted with 1 to 3 methoxy, ethoxy, or fluoro substituents.

4. The compound of claim 1 wherein R X is (C 1 -C 6 )alkyl optionally substituted with 1 to 3 methoxy, ethoxy, or fluoro substituents.

5. The compound of claim 1 wherein R X is methyl, ethyl, propyl, isopropyl, butyl, isobutyl or secbutyl, optionally substituted with methoxy or ethoxy or with 1 to 3 or fluoro substituents.

6. The compound of claim 1 wherein R X is methyl, ethyl, methoxymethyl, ethoxymethyl, methoxyethyl, ethoxyethyl, fluoromethyl, difluoromethyl, trifluoromethyl or trifluoromethoxymethyl.

7. The compound of claim 1 wherein R X is methyl, ethyl, methoxymethyl, fluoromethyl, difluoromethyl, or trifluoromethyl.

8. The compound of claim 1 wherein B is piperidin-3-yl or piperidin-4-yl.

9. The compound of claim 1 wherein B taken together with R X is 4-methylpiperidine-1,4-diyl.

10. The compound of claim 1 wherein: R 46 is alkyl or substituted alkyl; R 47 is alkyl, substituted alkyl, or heterocycle; or R 46 and R 47 together with the nitrogen atom to which they are attached form a heterocycle.

11. The compound of claim 1 wherein X is an alkylene group having from 3 to 20 carbon atoms; wherein one or more carbon atoms in the alkylene group is optionally replaced with —O—; and wherein the chain is optionally substituted on carbon with one or more hydroxyl groups.

12. The compound of claim 1 wherein X is nonane-1,9-diyl, octane-1,8-diyl, propane-1,3-diyl, 2-hydroxypropane-1,3-diyl, or 5-oxa-nonane-1,9-diyl.

13. The compound of claim 1 wherein X has the following formula:

wherein the phenyl ring is optionally substituted with 1, 2, or 3 fluoro groups.

14. The compound of claim 1 wherein X has one of the following formulas:

15. The compound of claim 1 wherein the compound has the formula:

or a pharmaceutically acceptable salt thereof.

16. The compound of claim 15 wherein X is an alkylene group having from 3 to 20 carbon atoms; wherein one or more carbon atoms in the alkylene group is optionally replaced with —O—; and wherein the chain is optionally substituted on carbon with one or more hydroxyl groups.

17. The compound of claim 15 wherein X is nonane-1,9-diyl, octane-1,8-diyl, propane-1,3-diyl,2-hydroxypropane-1,3-diyl, or 5-oxa-nonane-1,9-diyl.

18. The compound of claim 15 wherein X has the following formula:

wherein the phenyl ring is optionally substituted with 1,2, or 3 fluoro groups.

19. The compound of claim 15 wherein X has one of the following formulas:

20. The compound of claim 1 wherein R 46 is alkyl that is optionally substituted with from 1 to 5 substituents independently selected from the group consisting of alkoxy, substituted alkoxy, cycloalkyl, substituted cycloalkyl, cycloalkenyl, substituted cycloalkenyl, acyl, acylamino, acyloxy, amino, aminoacyl, aminoacyloxy, oxyaminoacyl, cyano, halo, hydroxyl, keto, thioketo, carboxyalkyl, thioaryloxy, thioheteroaryloxy, thioheterocyclooxy, thiol, thioalkoxy, substituted thioalkoxy, heterocycle, heterocyclooxy, hydroxyamino, alkoxyamino, and NR a R b , wherein R a and R b may be the same or different and are chosen from hydrogen, alkyl, substituted alkyl, cycloalkyl, alkenyl, cycloalkenyl, alkynyl, and heterocycle.

21. The compound of claim 1 wherein R 46 is 3-piperidinyl, 4-piperidinyl, or 3-pyrrolidinyl, which R 46 is optionally substituted with 1 to 3 substituents independently selected from the group consisting of alkoxy, substituted alkoxy, cycloalkyl, substituted cycloalkyl, cycloalkenyl, substituted cycloalkenyl, acyl, acylamino, acyloxy, amino, substituted amino, aminoacyl, aminoacyloxy, oxyaminoacyl, cyano, halo, hydroxyl, keto, thioketo, carboxyalkyl, thioaryloxy, thioheteroaryloxy, thioheterocyclooxy, thiol, thioalkoxy, substituted thioalkoxy, heterocycle, heterocyclooxy, hydroxyamino, alkoxyamino, alkyl, substituted alkyl, alkenyl, substituted alkenyl, alkynyl, and substituted alkynyl.

22. The compound of claim 1 wherein R 46 and R 47 together with the nitrogen atom to which they are attached form a piperidine or pyrrolidine ring which ring is optionally substituted with 1 to 3 substituents independently selected from the group consisting of alkoxy, substituted alkoxy, cycloalkyl, substituted cycloalkyl, cycloalkenyl, substituted cycloalkenyl, acyl, acylamino, acyloxy, amino, substituted amino, aminoacyl, aminoacyloxy, oxyaminoacyl, cyano, halo, hydroxyl, keto, thioketo, carboxyalkyl, thioaryloxy, thioheteroaryloxy, thioheterocyclooxy, thiol, thioalkoxy, substituted thioalkoxy, heterocycle, heterocyclooxy, hydroxyamino, alkoxyamino, alkyl, substituted alkyl, alkenyl, substituted alkenyl, alkynyl, and substituted alkynyl.

23. The compound of claim 1 wherein R 46 and R 47 together with the nitrogen atom to which they are attached form a heterocycle that is an aza-crown ether.

24. The compound of claim 23 wherein the aza-crown ether is 1-aza-12-crown-4,1-aza-15-crown-5, or 1-aza-18-crown-6.

25. A pharmaceutical composition comprising a pharmaceutically acceptable carrier and a therapeutically effective amount of a compound of claim 1 .

26. A compound having formula (V):

or a salt thereof.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 11, 2014
From: THERAVANCE, INC.
To: THERAVANCE BIOPHARMA R&D IP, LLC
Reel/Frame 033075/0370 →
MERGER Recorded Jun 14, 2002
From: ADVANCED MEDICINE, INC.
To: THERAVANCE, INC.
Reel/Frame 013005/0079 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 27, 2001
From: MAMMEN, MATHAI; OARE, DAVID
To: ADVANCED MEDICINE, INC.
Reel/Frame 011657/0481 →