IP Library Patent Application 13534875
Patent Application
App. No. 13/534,875

Substituted Indolealkanoic Acids

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Quick Facts
Patent No.
US None
App. No.
13/534,875
Abstract

Disclosed are substituted indolealkanoic acids useful in the treatment of chronic complications arising from diabetes mellitus. Also disclosed are pharmaceutical compositions containing the compounds and methods of treatment employing the compounds, as well as methods for their synthesis.

Claims (54)

1 . A compound of the formula:

or a pharmaceutically acceptable salt thereof, wherein

A is C 1 -C 4 alkyl;

Z is a bond;

R 1 is hydrogen, halogen, or alkyl having 1-6 carbon atoms;

R 3 is hydrogen, alkyl group of 1-6 carbon atoms, or halogen;

R 2 , R 4 and R 5 are independently hydrogen or halogen;

R 6 is hydroxy;

R a is hydrogen;

and Ar represents

a heterocyclic 5-membered ring having one nitrogen, two nitrogens one of which may be replaced by sulfur, said heterocyclic 5-membered ring optionally being condensed with benzo, said benzo being optionally substituted by one of iodo, cyano, nitro, perfluoroethyl, trifluoroacetyl, or (C 1 -C 6 )alkanoyl, one or two of fluoro, chloro, bromo, hydroxy, (C 1 -C 6 )alkyl, (C 1 -C 6 )alkoxy, (C 1 -C 6 )alkylthio, trifluoromethoxy, trifluoromethylthio, (C 1 -C 6 )alkylsulfinyl, (C 1 -C 6 )alkylsulfonyl or trifluoromethyl, or two fluoro or two trifluoromethyl with one hydroxy or one (C 1 -C 6 )alkoxy, or one or two fluoro and one trifluoromethyl, or three flour; or

a heterocyclic 6-membered ring having one to two nitrogen atoms, or one nitrogen atom and sulfur, said heterocyclic 6-membered ring optionally being condensed with benzo, said benzo being optionally substituted by one of iodo or trifluoromethylthio, or one or two of fluoro, chloro, bromo, (C 1 -C 6 )alkyl, (C 1 -C 6 )alkoxy, (C 1 -C 6 )alkylthio, (C 1 -C 6 )alkylsulfinyl, (C 1 -C 6 )alkylsulfonyl, or trifluoromethyl, and said pyridyl, furyl or thienyl optionally substituted in the 3-position by fluoro, chloro, (C 1 -C 6 )alkyl or (C 1 -C 6 )alkoxy.

2 . A compound according to claim 1 , wherein Ar represents

benzothiazolyl, quinolinyl, isoquinolinyl, quinoxalyl, or thiazolyl, each of which is optionally substituted with one of iodo, cyano, nitro, perfluoroethyl, trifluoroacetyl, or (C 1 -C 6 )alkanoyl, one or two of fluoro, chloro, bromo, hydroxy, (C 1 -C 6 )alkyl, (C 1 -C 6 )alkoxy, (C 1 -C 6 )alkylthio, trifluoromethoxy, trifluoromethylthio, (C 1 -C 6 )alkylsulfinyl, (C 1 -C 6 )alkylsulfonyl or trifluoromethyl, or two fluoro or two trifluoromethyl with one hydroxy or one (C 1 -C 6 )alkoxy, or one or, preferably, two fluoro and one trifluoromethyl, or three fluoro; or

phenyl group optionally substituted with up to 5 groups independently selected from halogen, an alkyl group of 1-6 carbon atoms (which may be substituted with one or more halogens), nitro, OR 7 , SR 7 , S(O)R 7 , S(O) 2 R 7 or N(R 7 ) 2 wherein R 7 is hydrogen, an alkyl group of 1-6 carbon atoms (which may be substituted with one or more halogens) or benzyl, where the phenyl portion is optionally substituted with up to three groups independently selected from halogen, C 1 -C 6 alkyl, C 1 -C 6 alkoxy, amino, and mono- or di(C 1 -C 6 )alkylamino.

3 . A compound according to claim 2 , wherein Ar is benzothiazolyl, quinolinyl, isoquinolinyl, quinoxalyl, or thiazolyl, each of which is optionally substituted with one trifluoromethyl or up to three fluoro groups.

4 . A compound according to claim 1 wherein at least one of R 1 and R 3 is not hydrogen;

5 . A compound according to claim 1 wherein R 2 , R 4 and R 5 are all hydrogen.

6 . A compound according to claim 1 wherein R 1 is hydrogen or alkyl having 1-6 carbon atoms.

7 . A compound according to claim 5 , wherein R 1 is hydrogen or methyl.

8 . A compound of the formula:

or a pharmaceutically acceptable salt thereof, wherein

A is methylene;

Z is a bond;

R 1 is hydrogen or alkyl having 1-6 carbon atoms;

R 3 is hydrogen or halogen;

provided that at least one of R 1 and R 3 is not hydrogen;

R 2 , R 4 and R 5 are all hydrogen;

R 6 is hydroxy;

R a is hydrogen;

and Ar represents

benzothiazolyl, quinolinyl, isoquinolinyl, quinoxalyl, or thiazolyl, each of which is optionally substituted with one of iodo, cyano, nitro, perfluoroethyl, trifluoroacetyl, or (C 1 -C 6 )alkanoyl, one or two of fluoro, chloro, bromo, hydroxy, (C 1 -C 6 )alkyl, (C 1 -C 6 )alkoxy, (C 1 -C 6 )alkylthio, trifluoromethoxy, trifluoromethylthio, (C 1 -C 6 )alkylsulfinyl, (C 1 -C 6 )alkylsulfonyl or trifluoromethyl, or two fluoro or two trifluoromethyl with one hydroxy or one (C 1 -C 6 )alkoxy, or one or, preferably, two fluoro and one trifluoromethyl, or three fluoro; or

phenyl group optionally substituted with up to 5 groups independently selected from halogen, an alkyl group of 1-6 carbon atoms (which may be substituted with one or more halogens), nitro, OR 7 , SR 7 , S(O)R 7 , S(O) 2 R 7 or N(R 7 ) 2 wherein R 7 is hydrogen, an alkyl group of 1-6 carbon atoms (which may be substituted with one or more halogens) or benzyl, where the phenyl portion is optionally substituted with up to three groups independently selected from halogen, C 1 -C 6 alkyl, C 1 -C 6 alkoxy, amino, and mono- or di(C 1 -C 6 )alkylamino.

9 . A compound according to claim 6 , where R 1 is hydrogen or methyl.

10 . A compound according to claim 8 , wherein Ar is benzothiazolyl, quinolinyl, isoquinolinyl, quinoxalyl, or thiazolyl, each of which is optionally substituted with one trifluoromethyl or up to three fluoro groups.

11 . A compound according to claim 8 , wherein Ar is phenyl substituted with one group.

12 . A compound according to claim 8 , wherein Ar is phenyl substituted with SO 2 R 7 .

13 . A compound according to claim 1 , which is:

2-methyl-3-(4,5,7-trifluorobenzothiazol-2-yl)methyl-indole-N-acetic acid;

5-chloro-3-(4,5,7-Trifluorobenzothiazol-2-yl)methyl-indole-N-acetic Acid; 5-fluoro-3-(4,5,7-trifluorobenzothiazol-2-yl)methyl-indole-N-acetic acid;

3-(3-nitrophenyl)methyl-indole-N-acetic acid;

5-Methyl-3-(5-Trifluoromethylbenzothiazol-2-yl)methyl-indole-N-acetic acid or

5-Bromo-3-(4,5,7-trifluorobenzothiazol-2-yl)methyl-indole-N-acetic acid.

14 . A compound of general formula (I):

wherein R 1 , R 3 and R 4 are hydrogen;

R 2 is halo;

R 5 and R 6 are hydrogen;

R 7 is C 1 -C 6 alkyl;

R 8 is a phenyl, naphthalenyl, thiazole, biphenyl, quinolinyl or quinoxalinyl group, any of which may be substituted with one or more halo, C 1 -C 6 alkyl, —O(C 1 -C 6 )alkyl, —SO 2 R 11 , or —OH groups;

wherein R 11 is independently hydrogen or C 1 -C 6 alkyl;

R 9 is hydrogen; or a pharmaceutically acceptable salt thereof.

15 . The compound of claim 14 , wherein, R 2 is fluoro; and R 7 methyl.

16 . A pharmaceutical composition comprising a compound of claim 14 together with a pharmaceutical excipient or carrier.

17 . A pharmaceutical composition, comprising a compound of claim 15 together with a pharmaceutical excipient or carrier.