N-SUBSTITUTE-2-OXODIHYDROPYRIDINE DERIVATIVES

Application 242/KOLNP/2005 published 2006-06-23, filed 2005-02-22
A compound of the formula (I): (wherein Ar1l and Ar2 are independently aryl or heteroaryl, any of which is optionally substituted by a substituent selected from the group consisting of cyano, halogen, nitro, lower alkyl, halo-lower alkyl, hydroxy-lower alkyl, cyclo-lower alkyl, cyclo(lower alkyl) -lower alkyl, lower alkenyl, lower alkylamino, di-lower alkylamino, lower alkanoylamino, lower alkylsulfonylamino, arylsulfonylamino, hydroxy, lower alkoxy, halo-lower alkoxy, aryloxy, heteroaryloxy, lower alkylthio, carboxyl, formyl, lower alkanoyl, lower alkoxycarbonyl, carbamoyl, lower alkylcarbamoyl, di-lower alkylcarbamoyl, lower alkylsulfonyl, arylsulfonyl, aryl and heteroaryl; R1 and R2 are independently lower alkyl, cyclo-lower alkyl, cyclo(lower alkyl)-lower alkyl or lower alkoxy, any of which is optionally substituted by a substituent selected from the group consisting of halogen, lower alkylamino, di-lower alkylamino, lower alkanoylamino, hydroxy, lower alkoxy, f ormyl, lower alkoxycarbonyl, lower alkylcarbamoyl and di-lower alkylcarbamoyl; R1 , R4 and R5 are independently hydrogen, cyano, halogen hydroxy, or lower alkyl, lower alkoxy or lower alkylthio, the last three groups being optionally substituted by a substituent selected from the group consisting of halogen, lower alkylamino, di -lower alkylamino, lower alkanoylamino, hydroxy, lower alkoxy, formyl, lower alkoxycarbonyl, lower alkylcarbamoyl and di-lower alkylcarbamoyl), or a salt or ester thereof is useful as a neuropeptide Y receptor antagonist agent and is also useful as an agent for the treatment of bulimia, obesity or diabetes. (FIG. – Nil)

Applicant

BANYU PHARMACEUTICAL CO LTTD
2-3 NIHONBASHI HONCHIO 2-CHOME CHUO-KU TOKYO 103-8416 JAPAN

Inventor

1. SATO NAGAAKI 2. ANDO MAKATO 3. ISHIKAWA SHIHO 4. NAGASE TSUYOSHI 5. NAGAI KEITA 6. KANATANI AKIO

International Info

Classification: C07D 401/14,401/04,213/80,A61K 31/444,A61P 3/04
Publication Number: WO 04/031175 A2
Application Date: 2003-09-25

Priority Information

2002-287015 JP 2002-09-30