IP Library › Granted Patent US 7,314,889
Granted Patent B2
US 7,314,889 · App. 10/306,898 · Granted Jan 1, 2008

Compounds and their use in medicine, process for their preparation and pharmaceutical compositions containing them

Assignees: Dr. Reddy's Laboratories, Inc.; Dr. Reddy's Laboratories Limited
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Quick Facts
Patent No.
US 7,314,889
App. No.
10/306,898
Granted
Jan 1, 2008
Kind
B2
Abstract

The present invention relates to novel antidiabetic, hypolipidemic, antiobesity and hypocholesterolemic compounds of formula (I), their derivatives, their analogs, their tautomeric forms, their stereoisomers, their polymorphs, their pharmaceutically acceptable salts, their pharmaceutically acceptable solvates and pharmaceutically acceptable compositions containing them.

Claims (72)

1. A compound of the formula (I)

wherein R 1 represents hydrogen, hydroxy, halogen, linear or branched (C 1 -C 12 ) alkyl, linear or branched (C 1 -C 12 ) alkoxy, or substituted or unsubstituted arylalkyl;

R 2 represents hydrogen, halogen, linear or branched (C 1 -C 12 ) alkyl, linear or branched (C 1 -C 12 ) alkoxy, (C 1 -C 12 ) alkanoyl, aroyl, arylalkanoyl, or substituted or unsubstituted arylalkyl;

R 3 represents hydrogen or a substituted or unsubstituted group which is linear or branched (C 1 -C 12 )alkyl, cycloalkyl, cycloalkylalkyl, cycloalkenyl, aryl, (C 1 -C 12 )alkanoyl, aroyl, arylalkyl, arylalkanoyl, alkoxyalkyl, alkoxycarbonyl, aryloxycarbonyl, alkylaminocarbonyl, or arylaminocarbonyl;

R 4 represents hydrogen;

Y represents oxygen;

R 5 represents hydrogen or a substituted or unsubstituted group which is alkyl, alkenyl, cycloalkyl, cycloalkylalkyl, aryl or arylalkyl;

Ar represents substituted or unsubstituted group which is divalent phenylene, or naphthylene;

X represents a bond;

R 6 represents —OSO 2 R 8 , —SO 2 R 8 , —SOR 8 , —SR 8 , —SO 2 NR 8 R 9 , or —SO 2 OR 8 , wherein R 8 and R 9 which may be the same or different, independently represent hydrogen, substituted or unsubstituted alkyl, aryl, arylalkyl, alkoxycarbonyl or arylalkoxycarbonyl; or with the provisio that R 6 is hydrogen, when R 13 is at the third position of the phenyl ring and does not represent hydrogen;

R 13 represents hydrogen, —OSO 2 R 8 , —SO 2 R 8 , —SOR 8 , —SR 8 , —SO 2 NR 8 R 9 , —SO 2 OR 8 , wherein R 8 and R 9 , which may be the same or different, independently represent hydrogen, substituted or unsubstituted alkyl, aryl, arylalkyl, alkoxycarbonyl or arylalkoxycarbonyl;

n is 1 to 6, and m is 0 to 6;

and stereoisomers, tautomeric forms, pharmaceutically acceptable salts, and pharmaceutically acceptable solvates of the compound of the formula (I).

2. The compound of formula (I) as claimed in claim 1 , wherein:

R 1 is hydrogen or linear or branched (C 1 -C 6 )alkyl;

R 2 is hydrogen or linear or branched (C 1 -C 6 )alkyl;

R 3 is hydrogen, linear or branched (C 1 -C 12 )alkyl, (C 3 -C 7 )cycloalkyl, aryl or arylalkyl;

R 4 hydrogen;

R 5 is hydrogen, (C 1 -C 12 )alkyl or (C 3 -C 7 )cycloalkyl;

R 6 is —OSO 2 R 8 ;

R 8 is hydrogen, linear or branched (C 1 -C 6 )alkyl or substituted or unsubstituted aryl;

R 9 is hydrogen, linear or branched (C 1 -C 6 )alkyl;

R 13 is hydrogen or —OSO 2 R 8 ;

X represents a bond;

Y is oxygen;

m is an integer from 0 to 1; and

n is an integer from 1 to 2.

3. The compound of formula (I) as claimed in claim 2 , wherein

R 1 is hydrogen;

R 2 is hydrogen;

R 3 is hydrogen, or linear or branched (C 1 -C 12 )alkyl;

R 4 is hydrogen;

R 5 is hydrogen or (C 1 -C 12 )alkyl;

R 6 is —OSO 2 R 8 ;

R 8 is or linear or branched (C 1 -C 6 )alkyl, or substituted aryl group wherein the substituent is linear or branched (C 1 -C 6 )alkyl;

R 9 is linear or branched (C 1 -C 6 )alkyl;

R 13 is hydrogen or —OSO 2 R 8 ; and

X represents a bond.

4. The compound according to claim 1 , wherein the pharmaceutically acceptable salt is selected from the group consisting of Li, Na, K, Ca, Mg, Fe, Cu, Zn, Al, Mn; N,N′-diacetylethylenediamine, betaine, caffeine, 2-diethylaminoethanol, 2-dimethylaminoethanol, N-ethylmorpholine, N-ethylpiperidine, glucamine, glucosamine, hydrabamine, isopropylamine, methylglucamine, morpholine, piperazine, piperidine, procaine, theobromine, valinol, diethylamine, triethylamine, trimethylamine, tripropylamine, tromethamine, adamentyl amine, diethanolamine, meglumine, ethylenediamine, N,N′-diphenylethylenediamine, N,N′-dibenzylethylenediamine, N-benzyl phenylethylamine, choline, choline hydroxide, dicyclohexylamine, metformin, benzylamine, phenylethylamine, dialkylamine, trialkylamine, thiamine, aminopyrimidine, aminopyridine, purine, pyrimidine, spermidine; alkylphenylamine, glycinol, phenyl glycinol; glycine, alanine, valine, leucine, isoleucine, norleucine, tyrosine, cystine, cysteine, methionine, proline, hydroxy proline, histidine, ornithine, lysine, arginine, serine, threonine, phenylalanine; unnatural amino acids; D-isomers or substituted amino acids; salts of acidic amino acids selected from aspartic acid or glutamic acid; guanidine, substituted guanidine wherein the substituents are selected from nitro, amino, alkyl, alkenyl or alkynyl; ammonium, substituted ammonium salts; sulphates, nitrates, phosphates, perchlorates, borates, hydrohalides (HCI, HBr, HI), acetates, tartrates, maleates, citrates, succinates, palmoates, methanesulphonates, benzoates, salicylates, hydroxynaphthoates, benzenesulfonates, ascorbates, glycerophosphates, or ketoglutarate salt.

5. The compound according to claim 1 , wherein the substituent on the group represented by R 3 is selected from the group consisting of hydrogen linear or branched groups selected from (C 1 -C 12 )alkyl, (C 3 -C 7 )cycloalkyl, aryl or arylalkyl.

6. The compound according to claim 1 , wherein the substituent on the group represented by R 5 is selected from the group consisting of hydrogen linear or branched groups selected from (C 1 -C 12 )alkyl, or (C 3 -C 7 )cycloalkyl.

7. The compound according to claim 1 , wherein the substituent on the group represented by R 6 is —OSO 2 R 8 .

8. The compound according to claim 1 , wherein the substituents on the group represented by R 13 are selected from the group consisting of hydrogen or —OSO 2 R 8 .

9. The compound according to claim 1 , wherein the substituents on the groups represented by, R 8 or R 9 are selected from the group consisting of hydrogen, linear or branched (C 1 -C 6 )alkyl, or substituted or unsubstituted aryl group wherein the substituent is linear or branched (C 1 -C 6 )alkyl.

10. A composition comprising a) the compound of claim 1 in accordance with the formula (I) its pharmaceutically acceptable salts, or its pharmaceutically acceptable solvates, and b) a pharmaceutically acceptable carrier, diluent, or excipients.

11. The composition of claim 10 , wherein, for said compound, said salt or said solvate,

R 1 is hydrogen, linear or branched (C 1 -C 6 )alkyl;

R 2 is hydrogen, linear or branched (C 1 -C 6 )alkyl;

R 3 is hydrogen, linear or branched (C 1 -C 12 )alkyl, (C 1 -C 7 )cycloalkyl;

R 4 is hydrogen;

R 5 is hydrogen, (C 1 -C 12 )alkyl or (C 3 -C 7 )cycloalkyl;

R 6 is —OSO 2 R 8 ;

R 8 is hydrogen, linear or branched (C 1 -C 6 )alkyl or substituted or unsubstituted aryl;

R 9 is hydrogen, linear or branched (C 1 -C 6 )alkyl, t-butyloxycarbonyl or benzyloxycarbonyl;

R 13 is hydrogen or —OSO 2 R 8 ;

X represents a bond;

Y is oxygen;

m is an integer from 0 to 1; and

n is an integer from 1 to 2.

12. The composition of claim 10 , wherein

R 1 hydrogen;

R 2 is hydrogen;

R 3 is hydrogen, or linear or branched (C 1 -C 12 )alkyl;

R 4 is hydrogen;

R 5 hydrogen or (C 1 -C 12 )alkyl;

R 6 is —OSO 2 R 8 ;

R 8 is or linear or branched (C 1 -C 6 )alkyl, or substituted aryl group wherein the substituent is linear or branched (C 1 -C 6 )alkyl;

R 9 is linear or branched (C 1 -C 6 )alkyl, t-butyloxycarbonyl or benzyloxycarbonyl;

R 13 is hydrogen or —OSO 2 R 8 ; and

X represents a bond.

13. The composition of claim 10 , which is in the form of a tablet, capsule, powder, syrup, solution or suspension.

14. The composition of claim 10 , further comprising insulin.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 1, 2003
From: DR. REDDY'S LABORATORIES LIMTED
To: DR. REDDY'S LABORATORIES INC.
Reel/Frame 014791/0035 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 26, 2003
From: DEBNATH, BHUNIYA; DAS, SAIBAL KUMAR; MADHAVAN, GURRAM RANGA; IQBAL, JAVED; CHAKRABARTI, RANJAN; VIKRAMADITHYAN, REEBA KANNIMEL
To: DR. REDDY'S LABORATORIES LIMITED
Reel/Frame 013893/0311 →
Priority Claims (1)
IN 971/MAS/2001 · Dec 3, 2001 · national
Continuity (1)
Related Publication 20030229083A1 · Dec 11, 2003