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Facile synthesis of 3-aryl-1-((4-aryl-1,2,3-selenadiazol-5-yl)sulfanyl)isoquinolines

โœ Scribed by Kamalakannan Prabakaran; Fazlur-Rahman Nawaz Khan; Jong Sung Jin; Euh Duck Jeong; Pitchai Manivel


Book ID
111491510
Publisher
Versita
Year
2011
Tongue
English
Weight
278 KB
Volume
65
Category
Article
ISSN
0366-6352

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โœฆ Synopsis


Abstract

A new series of 1,2,3-selenadiazoles containing an aryl or a 3-arylisoquinoline sulfanyl moiety at carbons 4 and 5, respectively, was prepared by cyclization of the respective semicarbazones in the presence of selenium(II) oxide and tetrahydrofuran at 70โ€“75ยฐC. Semicarbazones required for the reaction were obtained from 2-((3-arylisoquinolin-1-yl)sulfanyl)-1-phenylethanones, I, by a reaction with semicarbazide hydrochloride in ethanol/water mixture and potassium acetate base.


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Synthesis and characterization of 4-aryl
โœ Sivaperuman Saravanan; Arumugam Nithya; Shanmugam Muthusubramanian ๐Ÿ“‚ Article ๐Ÿ“… 2006 ๐Ÿ› Journal of Heterocyclic Chemistry ๐ŸŒ English โš– 294 KB

## Abstract magnified image magnified image The synthesis of a new set of selenadiazoles, 4โ€arylโ€5โ€(1โ€arylโ€2โ€methylโ€2โ€nitropropyl)โ€1,2,3โ€selenadiazoles (**4**) derived from 2โ€[4โ€methylโ€4โ€nitroโ€1,3โ€diarylpentylidene]โ€1โ€hydrazinecarboxamide (**3**) has been reported. THF has been found to be the so