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Title:
PYRIDADINONE, TRIAZINONE AND OXAPYRIDADINONE COMPOUND HAVING LIPOXYGENASE INHIBITING EFFECT
Document Type and Number:
Japanese Patent JPH01156966
Kind Code:
A
Abstract:

NEW MATERIAL: A compd. expressed by formula I and its salt wherein A is C=O or C=S; B is O, NR4 or CR5R6 (R4 is H, alkyl, OH, alkoxy, aryloxy, etc.; R5 and R6 are R2); R1 is aromatic carbon cyclic group or aromatic heterocyclic group with any substituents as desired and having 1 to 3 condensed or non-condensed ring each comprising 5 to 7 atoms; R2 is H, NR8R9 (R8, R9 is H or alkyl), halogen, alkyl, OH, CN, etc.; Z is H, pharmaceutically acceptable salt or metabolically cleavable group.

EXAMPLE: 1-(3-chlorophenyl)-2H,4H-tetrahydro-1,2,4-triazin-3-one.

USE: Lipoxygenase inhibitor.

PREPARATION: For example, a R1-substd. hydrazine is allowed to react with a R2-substd. haloethyl isocyanate expressed by formula II (X is halogen) to obtain a compd. expressed by formula III, which is then cyclized in a polar aprotic solvent to obtain a compd. expressed by formula IV.


Inventors:
DEII DABURIYU BURUTSUKUSU
JIYOOJI DABURIYUU KAATAA
ANWAA BATSUSHIYA
BURUUSU PII GAN
RICHIYAADO DEII DAIYAA
PURAMIRA EI BAATEIA
Application Number:
JP17889188A
Publication Date:
June 20, 1989
Filing Date:
July 18, 1988
Export Citation:
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Assignee:
ABBOTT LAB
International Classes:
A61K31/50; A61K31/52; A61K31/522; A61K31/53; A61K31/535; A61P11/00; A61P27/16; A61P29/00; A61P43/00; C07D237/04; C07D253/06; C07D273/04; C07D401/04; C07D401/10; C07D403/04; C07D403/10; C07D405/04; C07D405/10; C07D409/04; C07D413/04; C07D413/10; C07D417/04; C07D417/10; C07D473/08; (IPC1-7): A61K31/50; A61K31/52; A61K31/53; A61K31/535; C07D237/04; C07D253/06; C07D273/04; C07D401/04; C07D401/10; C07D403/04; C07D403/10; C07D405/04; C07D405/10; C07D409/04; C07D413/04; C07D413/10; C07D417/04; C07D417/10; C07D473/08
Attorney, Agent or Firm:
Aoyama Ryo (1 person outside)