Facile Synthesis of Benzo[d]azol-2(3H)-ones Using 2-Phenoxycarbonyl-4,5-dichloropyridazin-3(2H)-one as Green CO Source

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초록

Developing eco-friendly, stable, and easy-to-handle acyl sources is of great importance in synthetic and green chemistry. This study describes the synthesis of benzo[d]azol-2(3H)-ones such as benzo[d]thiazol-2(3H)-ones, benzo[d]oxazol-2(3H)-ones, and benzo[d]imidazol-2(3H)-ones using 2-phenoxycarbonyl-4,5-dichloropyridazin-3(2H)-one in one pot. The reaction reported is carried out under neutral or acidic conditions in the presence of zinc or sodium bicarbonate to give the corresponding heterocycles in good to excellent yields. The reaction uses a solid stable carbonyl source that is a recyclable functional-group carrier, pyridazin-3(2H)-one.

키워드

carbonylationgreen chemistryheterocyclesmedicinal chemistryring closure2(3H)-BENZOTHIAZOLONE DERIVATIVESRECEPTOR LIGANDSHIGHLY POTENT2(3H)-BENZOXAZOLONEDESIGNINHIBITORSDISCOVERYAGONISTSUREASD-2
제목
Facile Synthesis of Benzo[d]azol-2(3H)-ones Using 2-Phenoxycarbonyl-4,5-dichloropyridazin-3(2H)-one as Green CO Source
저자
Ryu, Ki EunKim, Bo RamSung, Gi HyeonYoon, Hyo JaeYoon, Yong-Jin
DOI
10.1055/s-0034-1378783
발행일
2015-09
유형
Article
저널명
Synlett
26
14
페이지
1985 ~ 1990