Convenient synthesis of substituted 3‐aminothiophene‐2‐carbonitriles from α‐acetylenic nitriles and their conversion to thieno[3,2‐d]pyrimidines Journal Article


Authors: Ren, W. Y.; Rao, K. V. B.; Klein, R. S.
Article Title: Convenient synthesis of substituted 3‐aminothiophene‐2‐carbonitriles from α‐acetylenic nitriles and their conversion to thieno[3,2‐d]pyrimidines
Abstract: Several novel 2,4,6‐trisubstituted thieno[3,2‐d]pyrimidines were synthesized from the hitherto unknown 3‐amino‐5‐methyl‐(or 5‐phenyl)thiophene‐2‐carbonitriles 7 and 8. o‐Aminonitriles 7 and 8 were obtained in a single step by conjugate addition of mercaptoacetonitrile (generated in situ) to substituted acetylenic nitriles 4 and 5 and annelation of the intermediate vinylic thioethers. Copyright © 1986 Journal of Heterocyclic Chemistry
Keywords: unclassified drug; drug efficacy; nonhuman; biological model; in vitro study; drug screening; drug synthesis; drug cytotoxicity; nuclear magnetic resonance; drug identification; intoxication; drug comparison; new drug; ultraviolet spectrophotometry; leukemia l 1210; thieno[3,2 d]pyrimidine derivative; blood and hemopoietic system; drug analysis; 2,4 diamino 6 phenylthieno[2,3 d]pyrimidine; 3 amino 2 thiophenecarbonitrile derivative; p 815 cell
Journal Title: Journal of Heterocyclic Chemistry
Volume: 23
Issue: 6
ISSN: 0022-152X
Publisher: Wiley-Blackwell Publishing, Inc.  
Date Published: 1986-11-01
Start Page: 1757
End Page: 1763
Language: English
DOI: 10.1002/jhet.5570230631
PROVIDER: scopus
DOI/URL:
Notes: Article -- Export Date: 18 August 2021 -- Source: Scopus
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  1. Robert S. Klein
    16 Klein