US2008058365A1PendingUtilityA1
Fused heterocyclic compounds
Est. expiryNov 6, 2022(expired)· nominal 20-yr term from priority
A61P 43/00A61P 25/24A61P 3/00A61P 3/04A61P 25/22A61P 25/20C07D 471/04A61K 31/435
56
PatentIndex Score
0
Cited by
0
References
0
Claims
Abstract
Compounds, compositions and methods are provided that are useful in the treatment and/or prevention of a condition or disorder mediated by a G-protein coupled receptor. In particular, the compounds of the invention are useful in the treatment and/or prevention of eating disorders, obesity, anxiety disorders and mood disorders.
Claims
exact text as granted — not AI-modified1 - 35 . (canceled)
36 . A method for treating a condition or disorder is selected from the group consisting of obesity, an eating disorder, an anxiety disorder and a mood disorder, comprising administering to a subject in need thereof a therapeutically effective amount of a compound of the formula (I):
wherein
represents a single or fused aryl or heteroaryl ring;
Q is —N(R)—(C 1 )alkylene-;
R is
L 1 is a bond, (C 1 -C 4 )alkylene, (C 1 -C 4 )alkylenoxy and (C 1 -C 4 )alkylenamino;
L 2 is a bond, (C 1 -C 4 )alkylene, (C 2 -C 4 )alkenylene, (C 2 -C 4 )alkynylene, (C 1 -C 4 )alkylenoxy or (C 1 -C 4 )alkylenamino;
R″ is hydrogen or (C 1 -C 8 )alkyl;
each R 1 is independently selected from the group consisting of halogen, (C 1 -C 8 )alkyl, (C 2 -C 8 )alkenyl, (C 2 -C 8 )alkynyl, fluoro(C 1 -C 4 )alkyl, —OR 5 , —SR 5 , fluoro(C 1 -C 4 )alkoxy, aryl, aryl(C 1 -C 4 )alkyl, —NO 2 , —NR 5 R 6 , —C(O)R 5 , —CO 2 R 5 , —C(O)NR 5 R 6 , —N(R 6 )C(O)R 5 , —N(R 6 )CO 2 R 5 , —N(R 7 )C(O)NR 5 R 6 , —S(O) m NR 5 R 6 , —S(O) m R 5 , —CN and —N(R 6 )S(O) m R 5 ;
R 2 and R 3 are independently selected from the group consisting of hydrogen, halogen, (C 1 -C 8 )alkyl, (C 2 -C 8 )alkenyl, (C 2 -C 8 )alkynyl, fluoro(C 1 -C 4 )alkyl, —OR 8 , —SR 8 , fluoro(C 1 -C 4 )alkoxy, aryl, aryl(C 1 -C 4 )alkyl, —NO 2 , —NR 8 R 9 , ═O, —C(O)R 8 , —CO 2 R 8 , —C(O)NR 8 R 9 , —N(R 9 )C(O)R 8 , —N(R 9 )CO 2 R 8 , —N(R 10 )C(O)NR 8 R 9 , —S(O) m NR 8 R 9 , —S(O) m R 8 , —CN and —N(R 9 )S(O) m R 8 ;
R 4 is selected from the group consisting of hydrogen, —OR 11 , —C(O)R 11 , —CO 2 R 11 , —C(O)NR 11 R 12 , —CN, (C 1 -C 4 )alkyl and aryl;
X and Y are independently selected from the group consisting of (C 1 -C 8 )alkyl, (C 2 -C 8 )alkenyl, (C 2 -C 8 )alkynyl, —CO 2 R 13 and —C(O)NR 13 R 14 ;
optionally, X and Y may be combined to form a 3-, 4-, 5-, 6- or 7-membered ring containing from 0 to 2 heteroatoms independently selected from the group consisting of N, O and S;
Z is selected from the group consisting of —OR 15 , —NR 15 R 16 , —NR 15 R 18 , —C(O)R 15 , —CO 2 R 15 , —R 18 , —C(O)NR 15 R 16 , —C(O)NR 15 R 18 , —SO 2 NR 15 R 16 , —SO 2 NR 15 R 18 , —NR 16 SO 2 R 15 , —N(R 15 )N(R 16 )SO 2 R 17 , —C(O)N(R 16 )OR 15 , hydroxy(C 1 -C 8 )alkyl, fluoro(C 1 -C 4 )alkyl, heteroaryl, —C(═NOR 15 )NR 16 R 17 , —C(R 16 )═NOR 15 , —NR 16 (OR 15 ), —C(O)NR 17 C(O)NR 15 R 16 , —NR 17 (C(O)NR 16 C(O)R 15 and —NR 17 C(O)NR 15 R 16 ;
R 5 , R 6 , R 7 , R 8 , R 9 , R 10 , R 11 , R 12 R 13 , R 14 , R 15 , R 16 and R 17 are independently selected from the group consisting of hydrogen, (C 1 -C 8 )alkyl, (C 2 -C 8 )alkenyl, (C 2 -C 8 )alkynyl, cyclo(C 3 -C 6 )alkyl, fluoro(C 1 -C 4 )alkyl, hetero(C 1 -C 4 )alkyl, cyclohetero(C 3 -C 6 )alkyl, aryl and aryl(C 1 -C 4 )alkyl;
R 18 is a 5- or 6-membered ring containing from 0 to 4 heteroatoms selected from the group consisting of N, O and S (e.g. tetrazole);
optionally, when two R groups selected from the group consisting of R 5 , R 6 , R 8 , R 9 , R 11 , R 12 , R 13 , R 14 , R 15 , R 16 and R 17 are attached to the same nitrogen atom, the R groups may be combined to form a 3-, 4-, 5-, 6- or 7-membered ring containing the nitrogen atom and from 0 to 2 additional heteroatoms selected from the group consisting of N, O and S;
the subscript m is 1 or 2, and
the subscript n is 0, 1 or 2.
37 . The method of claim 36 , wherein said compound condition or disorder is selected from the group consisting of obesity, anorexia nervosa, anxiety, panic disorder and obsessive-compulsive disorder and depression.
38 . The method of claim 36 , wherein said compound is administered in combination with an anti-obesity agent, an antidepressant or an anxiolytic agent.
39 . The method of claim 36 , wherein said compound is administered orally.
40 . The method of claim 36 , wherein said compound is administered parenterally.
41 . The method of claim 36 , wherein said compound modulates MCHR.
42 . A method for modifying eating behavior, comprising administering to a subject in need thereof a therapeutically effective amount of a compound of the formula (I):
wherein
represents a single or fused aryl or heteroaryl ring;
Q is —N(R—(C 1 )alkylene-;
R is
L 1 is a bond, (C 1 -C 4 )alkylene, (C 1 -C 4 )alkylenoxy and (C 1 -C 4 )alkylenamino;
L 2 is a bond, (C 1 -C 4 )alkylene, (C 2 -C 4 )alkenylene, (C 2 -C 4 )alkynylene, (C 1 -C 4 )alkylenoxy or (C 1 -C 4 )alkylenamino;
R″ is hydrogen or (C 1 -C 8 )alkyl;
each R 1 is independently selected from the group consisting of halogen, (C 1 -C 8 )alkyl, (C 2 -C 8 )alkenyl, (C 2 -C 8 )alkynyl, fluoro(C 1 -C 4 )alkyl, —OR 5 , —SR 5 , fluoro(C 1 -C 4 )alkoxy, aryl, aryl(C 1 -C 4 )alkyl, —NO 2 , —NR 5 R 6 , —C(O)R 5 , —CO 2 R 5 , —C(O)NR 5 R 6 , —N(R 6 )C(O)R 5 , —N(R 6 )CO 2 R 5 , —N(R 7 )C(O)NR 5 R 6 , —S(O) m NR 5 R 6 , —S(O) m R 5 , —CN and —N(R 6 )S(O) m R 5 ;
R 2 and R 3 are independently selected from the group consisting of hydrogen, halogen, (C 1 -C 8 )alkyl, (C 2 -C 8 )alkenyl, (C 2 -C 8 )alkynyl, fluoro(C 1 -C 4 )alkyl, —OR 8 , —SR 8 , fluoro(C 1 -C 4 )alkoxy, aryl, aryl(C 1 -C 4 )alkyl, —NO 2 , —NR 8 R 9 , ═O, —C(O)R 8 , —CO 2 R 8 , —C(O)NR 8 R 9 , —N(R 9 )C(O)R 8 , —N(R 9 )CO 2 R 8 , —N(R 10 )C(O)NR 8 R 9 , —S(O) m NR 8 R 9 , —S(O) m R 8 , —CN and —N(R 9 )S(O) m R 8 ;
R 4 is selected from the group consisting of hydrogen, —OR 11 , —C(O)R 11 , —CO 2 R 11 , —C(O)NR 11 R 12 , —CN, (C 1 -C 4 )alkyl and aryl;
X and Y are independently selected from the group consisting of (C 1 -C 8 )alkyl, (C 2 -C 8 )alkenyl, (C 2 -C 8 )alkynyl, —CO 2 R 13 and —C(O)NR 13 R 14 ;
optionally X and Y may be combined to form a 3-, 4-, 5-, 6- or 7-membered ring containing from 0 to 2 heteroatoms independently selected from the group consisting of N, O and S;
Z is selected from the group consisting of —OR 15 , —NR 15 R 16 , —NR 15 R 18 , —C(O)R 15 , —CO 2 R 15 , —R 18 , —C(O)NR 15 R 16 , —C(O)NR 15 R 18 , —SO 2 NR 15 R 16 , —SO 2 NR 15 R 18 , —NR 16 SO 2 R 15 , —N(R 15 )N(R 16 )SO 2 R 17 , —C(O)N(R 16 )OR 15 , hydroxy(C 1 -C 8 )alkyl, fluoro(C 1 -C 4 )alkyl, heteroaryl, —C(═NOR 15 )NR 16 R 17 , —C(R 16 )═NOR 15 , —NR 16 (OR 15 ), —C(O)NR 17 C(O)NR 15 R 16 , —NR 17 C(O)NR 16 C(O)R 15 and —NR 17 C(O)NR 15 R 16 ;
R 5 , R 6 , R 7 , R 8 , R 9 , R 10 , R 11 , R 12 , R 13 , R 14 , R 15 , R 16 and R 17 are independently selected from the group consisting of hydrogen, (C 1 -C 8 )alkyl, (C 2 -C 8 )alkenyl, (C 2 -C 8 )alkynyl, cyclo(C 3 -C 6 )alkyl, fluoro(C 1 -C 4 )alkyl, hetero(C 1 -C 4 )alkyl, cyclohetero(C 3 -C 6 )alkyl, aryl and aryl(C 1 -C 4 )alkyl;
R 18 is a 5- or 6-membered ring containing from 0 to 4 heteroatoms selected from the group consisting of N, O and S (e.g. tetrazole);
optionally when two R groups selected from the group consisting of R 5 , R 6 , R 8 , R 9 , R 11 , R 12 , R 13 , R 14 , R 15 , R 16 and R 17 are attached to the same nitrogen atom, the R groups may be combined to form a 3-, 4-, 5-, 6- or 7-membered ring containing the nitrogen atom and from 0 to 2 additional heteroatoms selected from the group consisting of N, O and S;
the subscript m is 1 or 2: and
the subscript n is 0, 1 or 2.
43 . The method of claim 42 , wherein food intake is decreased.
44 . The method of claim 42 , wherein food intake is increased.
45 . A method for treating a condition or disorder mediated by MCHR, comprising administering to a subject in need thereof a therapeutically effective amount of a compound of the formula (I):
wherein
represents a single or fused aryl or heteroaryl ring,
Q is —N(R)—(C 1 )alkylene-;
R is
L 1 is a bond, (C 1 -C 4 )alkylene, (C 1 -C 4 )alkylenoxy and (C 1 -C 4 )alkylenamino;
L 2 is a bond, (C 1 -C 4 )alkylene, (C 2 -C 4 )alkenylene, (C 2 -C 4 )alkynylene, (C 1 -C 4 )alkylenoxy or (C 1 -C 4 )alkylenamino;
R″ is hydrogen or (C 1 -C 8 )alkyl;
each R 1 is independently selected from the group consisting of halogen, (C 1 -C 8 )alkyl, (C 2 -C 8 )alkenyl, (C 2 -C 8 )alkynyl, fluoro(C 1 -C 4 )alkyl, —OR 5 , —SR 5 , fluoro(C 1 -C 4 )alkoxy, aryl, aryl(C 1 -C 4 )alkyl, —NO 2 , —NR 5 R 6 , —C(O)R 5 , —CO 2 R 5 , —C(O)NR 5 R 6 , —N(R 6 )C(O)R 5 , —N(R 6 )CO 2 R 5 , —N(R 7 )C(O)NR 5 R 6 , —S(O) m NR 5 R 6 , —S(O) m R 5 , —CN and —N(R 6 )S(O) m R 5 ;
R 2 and R 3 are independently selected from the group consisting of hydrogen, halogen, (C 1 -C 8 )alkyl, (C 2 -C 8 )alkenyl, (C 2 -C 8 )alkynyl, fluoro(C 1 -C 4 )alkyl, —OR 8 , —SR 8 , fluoro(C 1 -C 4 )alkoxy, aryl aryl(C 1 -C 4 )alkyl, —NO 2 , —NR 8 R 9 , ═O, —C(O)R 8 , —CO 2 R 8 , —C(O)NR 8 R 9 , —N(R 9 )C(O)R 8 , —N(R 9 )CO 2 R 8 , —N(R 10 )C(O)NR 8 R 9 , —S(O) m NR 8 R 9 , —S(O) m R 8 , —CN and —N(R 9 )S(O) m R 8 ;
R 4 is selected from the group consisting of hydrogen, —OR 11 , —C(O)R 11 , —CO 2 R 11 , —C(O)NR 11 R 12 , —CN, (C 1 -C 4 )alkyl and aryl;
X and Y are independently selected from the group consisting of (C 1 -C 8 )alkyl, (C 2 -C 8 )alkenyl, (C 2 -C 8 )alkynyl, —CO 2 R 13 and —C(O)NR 13 R 14 ;
optionally, X and Y may be combined to form a 3-, 4-, 5-, 6- or 7-membered ring containing from 0 to 2 heteroatoms independently selected from the group consisting of N, O and S;
Z is selected from the group consisting of —OR 15 , —NR 15 R 16 , —NR 15 R 18 , —C(O)R 15 , —CO 2 R 15 , —R 18 , —C(O)NR 15 R 16 , —C(O)NR 15 R 18 , —SO 2 NR 15 R 16 , —SO 2 NR 15 R 18 ; —NR 16 SO 2 R 15 , —N(R 15 )N(R 16 )SO 2 R 17 , —C(O)N(R 16 )OR 15 , hydroxy(C 1 -C 8 )alkyl, fluoro(C 1 -C 4 )alkyl, heteroaryl, —C(═NOR 15 )NR 16 R 17 , —C(R 16 )═NOR 15 , —NR 16 (OR 15 ), —C(O)NR 17 C(O)NR 15 R 16 , —NR 17 C(O)NR 16 C(O)R 15 and —NR 17 C(O)NR 15 R 16 ;
R 5 , R 6 , R 7 , R 8 , R 9 , R 10 , R 11 , R 12 , R 13 , R 14 , R 15 , R 16 and R 17 are independently selected from the group consisting of hydrogen, (C 1 -C 8 )alkyl, (C 2 -C 8 )alkenyl, (C 2 -C 8 )alkynyl, cyclo(C 3 -C 6 )alkyl, fluoro(C 1 -C 4 )alkyl, hetero(C 1 -C 4 )alkyl, cyclohetero(C 3 -C 6 )alkyl, aryl and aryl(C 1 -C 4 )alkyl;
R 18 is a 5- or 6-membered ring containing from 0 to 4 heteroatoms selected from the group consisting of N, O and S (e.g. tetrazole);
optionally, when two R groups selected from the group consisting of R 5 , R 6 , R 8 , R 9 , R 11 , R 12 , R 13 , R 14 , R 15 , R 16 and R 17 are attached to the same nitrogen atom, the R groups may be combined to form a 3-, 4-, 5-, 6- or 7-membered ring containing the nitrogen atom and from 0 to 2 additional heteroatoms selected from the group consisting of N, O and S;
the subscript m is 1 or 2; and
the subscript n is 0, 1 or 2.
46 . The method of claim 45 , wherein said condition or disorder is selected from the group consisting of obesity, an eating disorder, an anxiety disorder and a mood disorder.
47 . The method of claim 46 , wherein said eating disorder is anorexia nervosa.
48 . The method of claim 46 , wherein said anxiety disorder is selected from the group consisting of anxiety, panic disorder and obsessive-compulsive disorder.
49 . The method of claim 46 , wherein said mood disorder is depression.
50 - 52 . (canceled)
53 . The method of claim 36 , wherein said compound is selected from the group consisting of:Join the waitlist — get patent alerts
Track US2008058365A1 — get alerts on status changes and closely related new filings.
We store only your email — no account needed. See our privacy policy.