313353-02-5Relevant articles and documents
Transamination of cyanothioacetamide with morpholine. molecular and crystal structure of 3-(morpholin-1-yl)-3-thioxopropanenitrile and 3-(morpholin-1-yl)- 3-thioxopropanethioamide
Dyachenko,Chernega,Dyachenko
, p. 720 - 724 (2012)
Transamination of cyanothioacetamide with equimolar amount of morpholine resulted in the formation of 3-(morpholin-1-yl)-3-thioxopropanenitrile, and with twofold excess of morpholine 3-(morpholin-1-yl)-3-thioxopropanethioamide was obtained. By the alkylation of the resulting products 2-[2-(morpholin-1-yl)-2- thioxoethylidene]thiazolidin-4-one, 3-amino-N-(4-acetylphenyl)-5-(morpholin-1- yl)-thiophene-2-carbox-amide, 3-amino-3-methylthio-1-morpholinoprop-2-ene-1- thione, (2E,4E)-2-(morpholin-4-yl)thiocarbonyl)-5-phenylpenta-2,4- dienothioamide, and 3-{2′-[2″-(molrpholin-1-yl)-2-thioxoethyl] thiazol-4′-yl}-2H-chromen-2-one were synthesized. The 3-(morpholin-1-yl)- 3-thioxopropanenitrile and 3-(morpholin-1-yl)-3-thioxopropane-thioamide structures were studied by the X-ray diffraction.