Facile synthesis of 3-aryl-1-((4-aryl-1,2,3-selenadiazol-5-yl)sulfanyl)isoquinolines
โ 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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โฆ 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 70โ75ยฐC. 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.
๐ SIMILAR VOLUMES
## Abstract magnified image magnified image The synthesis of a new set of selenadiazoles, 4โarylโ5โ(1โarylโ2โmethylโ2โnitropropyl)โ1,2,3โselenadiazoles (**4**) derived from 2โ[4โmethylโ4โnitroโ1,3โdiarylpentylidene]โ1โhydrazinecarboxamide (**3**) has been reported. THF has been found to be the so