发明名称 NEW PIRIDAZINE DERIVATIVE AND MEDICINE CONTAINING THE SAME AS ACTIVE INGREDIENT
摘要 PROBLEM TO BE SOLVED: To obtain the subject new derivative excellent in suppressing action on a specific interleukin production, and useful as a preventing and treating agent for an immune system disease, an inflammatory disease, an ischemic disease, or the like. SOLUTION: This new piridazine derivative is a compound of formula I [R1 is a (substituted) aryl; R2 is a phenyl substituted at least with a lower alkoxy or the like at its 4 position and other positions thereof are substitutable; R3 is H or the like; A is a single bond or the like; X is O or the like; a broken line is a single bond or the like; provided that such conditions must be satisfied when the R3 is a halogenated lower alkyl, the A is a single bond, or the like], preferably 5,6-bis(4-methoxyphenyl)-2-(4-chlorocinnamyl)-2H-piridazin-3-one, or the like. The compound of formula I is obtained e.g. by reacting a compound of formula II with glyoxalic acid, reacting a hydrated hydrazine with the obtained compound, then performing dehydration reaction, and then reacting the obtained compound of formula III with a compound of the formula: R3-A-Y (Y is a halogen). The obtained compound has an interleukin-1βproduction- suppressing activity.
申请公布号 JP2000198776(A) 申请公布日期 2000.07.18
申请号 JP19980319281 申请日期 1998.11.10
申请人 KOWA CO 发明人 OGUCHI MASAO;KYOTANI YOSHINORI;SHIGYO HIROMICHI;KOSHI TOMOYUKI;KITAMURA TAKAHIRO;OGIYA TADAAKI;MATSUDA TAKAYUKI;YAMAZAKI YUKIYOSHI;KUMAI NATSUYO;KOTAKI KYOKO
分类号 C07D237/04;A61K31/00;A61K31/50;A61K31/535;A61K31/5375;A61K31/5377;A61P1/00;A61P1/16;A61P9/00;A61P9/10;A61P13/00;A61P19/10;A61P29/00;A61P31/00;A61P37/00;A61P37/02;A61P43/00;C07D237/14;C07D401/04;C07D401/06;(IPC1-7):C07D237/14;A61K31/537 主分类号 C07D237/04
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