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Synthesis, characterization and biological screening of various pharmacophoric derivatives of 4-alkylpyrimidine-5-carbonitrile

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Title Synthesis, characterization and biological screening of various pharmacophoric derivatives of 4-alkylpyrimidine-5-carbonitrile
 
Creator Thanki, Pragna H
Hingrajia, Dhaval V
Modha, Jayesh J
 
Subject Derivatives of 4-isobutyl-1
6-dihydro-1-Methyl-6-oxo pyrimidine-5-carbonitrile
antimicrobial
anticancer
CO-ADD
DTP
 
Description 81-87
4-Isobutyl-1,6-dihydro-1-methyl-2-(methylthio)-6-oxopyrimidine-5-carbonitrile has been used as a starting material.
Reaction of 4-isobutyl-1,6-dihydro-1-methyl-2-(methylthio)-6-oxopyrimidine-5-carbonitrile with hydrazine hydrate and
amine gives 2-hydrazino and 2-(alkyl/ substituted aryl amino)-4-isobutyl-1,6-dihydro-1-methyl-6-oxopyrimidine-5-
carbonitrile compounds respectively. The hydrazino compounds react with different aromatic aldehydes, substituted benzene
sulphonyl chloride and s-triazine derivative to form Schiff base, sulphonamide and s-triazine derivatives respectively.
Reaction of Schiff base with mercapto lactic acid and chloroacetyl chloride yield 4-thiazolidinones and 2-azetidinones
respectively.
 
Date 2022-02-01T10:40:57Z
2022-02-01T10:40:57Z
2022-01
 
Type Article
 
Identifier 2583-1321 (Online); 0019-5103 (Print)
http://nopr.niscair.res.in/handle/123456789/59036
 
Language en
 
Publisher NIScPR-CSIR, India
 
Source IJC Vol.61(01) [January 2022]