Synthesis of N-methylmorpholinium 6-methyl-4-(2-thienyl)-5-phenylcarbamoyl-3-cyano-1,4-dihydropyridine-2-thiolate and its reaction with various functionally substituted methyl halides

2Citations
Citations of this article
2Readers
Mendeley users who have this article in their library.
Get full text

Abstract

Condensation of the anilide of acetoacetic acid, thiophene aldehyde, cyanothioacetamide and N-methylmorpholine gave N-methylmorpholinium 6-methyl-4-(2-thienyl)-5-phenylcarbamoyl-3-cyano-1,4-dihydropyridine-2-thiolate which reacted with various halides ZCH2Hal or H2NCOCH(Ph)Cl to give substituted 2-ZCH2-thio or 2-H2NCOCH(Ph)-thio-1,4-dihydropyridines. ©1997 Plenum Publishing Corporation.

Cite

CITATION STYLE

APA

Dyachenko, V. D., Krivokolysko, S. G., & Litvinov, V. P. (1997). Synthesis of N-methylmorpholinium 6-methyl-4-(2-thienyl)-5-phenylcarbamoyl-3-cyano-1,4-dihydropyridine-2-thiolate and its reaction with various functionally substituted methyl halides. Chemistry of Heterocyclic Compounds, 33(5), 577–582. https://doi.org/10.1007/BF02291942

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free