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Title:
SUBSTITUTED CARBOXYTETRAHYDROISOQUINOLINE AND DERIVATIVE OF THE SAME HAVING PHERMACEUTICAL ACTIVITY
Document Type and Number:
Japanese Patent JPH03120254
Kind Code:
A
Abstract:

NEW MATERIAL: A compound of formula [R1 is H or a protecting group; R2 and R3 are H, alkyl, aryl, COOR4 (R4 is H, alkyl, alkenyl or the like), or the like with the proviso that one of them is COOR4; R5 is OH when R3 is COOR4, and is H, alkyl, aryl or the like when R2 is COOR4; R6 and R7 are each H, OH, alkoxy, alkyl, aryl or the like; B is phenyl, 5-6 membered heteroaryl ring; X is (CH2)n (n is 0-2), OCH2, NHCH2, SOCH2 or the like; A is OPO3R8R9 (R8 and R9 are each H, alkyl, alkenyl or the like), BO2R8R9, tetrazole, or the like].

EXAMPLE: 1,2,3,4-Tetrahydro-5-phosphono-3-isoquinoline carboxylic acid.

USE: Effectively used for the medical treatment of a disease relating to the blockade of stimulus concentrated amino acid receptor.

PROCESS: A solution of dimethyl 5-(diethoxyphosfinyl)-3,4-dihydro-2,3(1H)- isoquinoline dicarboxylate, is heated under the reflux, to obtain the compound of the example.


Inventors:
GUREIAMU JIYONSON
TOMASU CHIYAARUZU MAROUN
Application Number:
JP26327690A
Publication Date:
May 22, 1991
Filing Date:
October 02, 1990
Export Citation:
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Assignee:
WARNER LAMBERT CO
International Classes:
C07D217/22; A61K31/41; A61K31/47; A61K31/472; A61K31/473; A61K31/675; A61P9/00; C07B61/00; C07C271/22; C07D217/26; C07D221/04; C07D401/06; C07D401/12; C07D495/04; C07F9/40; C07F9/62; C07F9/6561; (IPC1-7): A61K31/41; A61K31/47; A61K31/675; C07B61/00; C07D217/22; C07D221/04; C07D401/06; C07D401/12; C07F9/62; C07F9/6561
Attorney, Agent or Firm:
Chika Takagi (2 outside)