Substituted indolealkanoic acids
View Patent ↗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.
1. A compound of the formula:
wherein
A is a C 1 -C 4 alkylene group;
Z is a bond or C 1 -C 3 alkylene;
R 1 is hydrogen, alkyl having 1-6 carbon atoms, halogen, 2-, 3-, or 4-pyridyl, or phenyl, where the phenyl or pyridyl is optionally substituted with up to three groups selected from halogen, hydroxy, C 1 -C 6 alkoxy, C 1 -C 6 alkyl, nitro, amino, or mono- or di(C 1 -C 6 )alkylamino;
R 2 , R 3 , R 4 and R 5 are each independently hydrogen, halogen, nitro, or an alkyl group of 1-6 carbon atoms optionally substituted with one or more halogens;
OR 7 , SR 7 , S(O)R 7 , S(O) 2 N(R 7 ) 2 , C(O)N(R 7 ) 2 , or N(R 7 ) 2 , wherein each R 7 is independently hydrogen, an alkyl group of 1-6 carbon atoms optionally 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;
phenyl or heteroaryl, where each of which phenyl or heteroaryl 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;
phenoxy 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; or
a group of the formula
where
J is a bond, CH 2 , oxygen, or nitrogen; and
each r is independently 2 or 3;
R 6 is hydroxy, benzyloxy, di(C 1 -C 6 )alkylaminoethyloxy, acetoxymethyl, pivaloyloxymethyl, phthalidoyl, ethoxycarbonyloxyethyl, 5-methyl-2-oxo-1,3-dioxol-4-ylmethyl, C 1 -C 6 alkoxy or O − M + where M + represents a cation selected from sodium, potassium, ammonium, magnesium and calcium;
R a is hydrogen or C 1 -C 6 alkyl;
and Ar represents
a phenyl group substituted nitro, SR 7 , S(O)R 7 , or S(O) 2 R 7 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 of the benzyl group 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.
2. A compound according to claim 1 , wherein Ar is a substituted phenyl of Formula II
wherein R 8 , R 8 ′, R 9 , R 9 ′, and R 10 are independently hydrogen, fluorine, chlorine, bromine, trifluoromethyl or nitro.
3. A compound according to claim 2 , wherein A is methylene and Z is a bond.
4. A compound according to claim 2 , wherein R a is hydrogen and Z is a bond.
5. A compound according to claim 2 , wherein A is methylene, R a is hydrogen, and Z is a bond.
6. A compound according to claim 5 , wherein R 6 is hydroxy.
7. A compound according to claim 5 , wherein R 6 is C 1 -C 6 alkoxy.
8. A compound according to claim 5 , wherein Ar is phenyl substituted with nitro or SO 2 R 7 .
9. A compound according to claim 8 , wherein at least one of R 8 , R 8′ , R 9 , R 9′ , R 10 is trifluoromethyl.
10. A compound according to claim 9 , wherein R 9 is trifluoromethyl.
11. A compound according to claim 10 , wherein R 8 , R 8′ , R 9 , R 9′ , R 10 are fluorines and R 13 is hydrogen.
12. A compound according to claim 11 , wherein R 6 is hydroxy.
13. A compound according to claim 11 , wherein R 6 is C 1 -C 6 alkoxy.
14. A compound according to claim 1 , which is 3-(3-nitrophenyl)methyl-indole-N-acetic acid.
15. A compound according to claim 1 , which is 3-(3-nitrophenyl)methyl-indole-N-acetic acid, ethyl ester.