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The conversion of [(4-chloro-5H-1,2,3-dithiazol-5-ylidene)amino]azines into azine fused thiazole-2-carbonitriles

โœ Scribed by Koutentis, Panayiotis A. ;Koyioni, Maria ;Michaelidou, Sophia S.


Book ID
118135163
Publisher
Royal Society of Chemistry
Year
2013
Tongue
English
Weight
336 KB
Volume
11
Category
Article
ISSN
1477-0520

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-vlidene derivatives 1-3 with primary and secovdary alkylarmnes in CH,CL at room temperature gave 2,5-dzhydro-2-iminopyrroles (22-55%) and 2, 5-dihydro-2-imino[urans (18-62%). However, similar treatment of alltyl (4-chloro-5H-1,2,3dithtazol-5-ylidene)cyanoacetates under the same conditions gave (Z)-