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Title:
THIADIAZOLE ANTIVIRAL AGENT
Document Type and Number:
Japanese Patent JPH02292297
Kind Code:
A
Abstract:

NEW MATERIAL: A compound (a salt) represented by formula I, wherein R denotes H, CN, formula II (wherein R1 denotes a 1-6C alkyl, a cyano-1-6C alkyl or a pyridyl-1-6C alkyl), etc.; and R2 denotes H or a hydroxy protecting group.

EXAMPLE: 1,3,4-Thiadiazol-2-ylcyanamide-3-β-D-ribofuranose.

USE: A therapeutic agent for viral infection.

PROCESS: A solution of β-D-ribofuranose compound (such as β-D- ribofuranose-1,2,3,5-tetraacetate, etc.), is added to a solution where dry HBr is saturated in dry methylene chloride, and the like for reaction to obtain a derivative represented by formula III (wherein X denotes an eliminable group). Then, it is reacted with 2-amino-1,3,4-thiadiazole represented by formula IV (wherein R3 denotes H; and R denotes H, cyano, etc.), and optionally deprotected to obtain a compound represented by formula I.


Inventors:
MARII TERESA RIIMAA
UEIN ARUFURETSUDO SUPITSUTSUAA
FURANTSU BIKUTAA
Application Number:
JP9742890A
Publication Date:
December 03, 1990
Filing Date:
April 12, 1990
Export Citation:
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Assignee:
LILLY CO ELI
International Classes:
A61K31/70; A61K31/7042; A61K31/7052; A61P31/12; C07H19/24; (IPC1-7): A61K31/70; C07H19/24
Attorney, Agent or Firm:
Aoyama Ryo (1 person outside)