z-logo
Premium
One‐Pot Synthesis of Pyrido[2,3‐ d ]Pyrimidine‐2‐Thiones and a Study of Their Reactivity Towards Some Reagents
Author(s) -
ElGazzar A. B. A.,
Hafez H. N.,
Yakout E. M. A.
Publication year - 2007
Publication title -
journal of the chinese chemical society
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.329
H-Index - 45
eISSN - 2192-6549
pISSN - 0009-4536
DOI - 10.1002/jccs.200700184
Subject(s) - chemistry , malononitrile , reagent , pyrimidine , aldehyde , formamide , reactivity (psychology) , organic chemistry , combinatorial chemistry , medicinal chemistry , stereochemistry , catalysis , medicine , alternative medicine , pathology
A series of pyrido[2,3‐ d ]pyrimidine‐2‐thione derivatives ( 5a‐c ) were synthesized by the one‐pot reaction of the appropriate aldehyde, malononitrile and 6‐aminothiouracil ( 1 ) in dimethyl‐formamide. The same compounds were also synthesized by the reaction of arylidine malononitrile ( 4 ) with 6‐aminothiouracil ( 1 ). Moreover, the chemical behaviour of the produced pyrimidines towards different reagents was studied.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom