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Reaction of nitriles under acidic conditions. Part III. A facile synthesis of thienopyrimidin‐4(3 H )‐ones
Author(s) -
Shishoo C. J.,
Devani M. B.,
Pathak U. S.,
Ananthan S.,
Bhadti V. S.,
Ullas G. V.,
Jain K. S.,
Rathod I. S.,
Talati D. S.,
Doshi N. H.
Publication year - 1984
Publication title -
journal of heterocyclic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.321
H-Index - 59
eISSN - 1943-5193
pISSN - 0022-152X
DOI - 10.1002/jhet.5570210220
Subject(s) - chemistry , yield (engineering) , acetonitrile , thiophene , organic chemistry , reaction conditions , medicinal chemistry , catalysis , materials science , metallurgy
A variety of thiophene o ‐aminoesters were reacted with cyanates, thiocyanates, cyanamides, acyl cyanides and α‐functionalized acetonitrile derivatives to yield the corresponding 2‐substituted thienopyrimidin‐4(3 H )‐ones.