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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 416611생성일: 2026년 10월 23일

Ethyl 2-aminothiazole-4-carboxylate → Ethyl 6-(2-nitrophenyl)imidazo[2,1-b]thiazole-3-carboxylate

https://huagongshe.com/ko/reaction/416611

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl 2-aminothiazole-4-carboxylateHCID 73216—
반응물2-Bromo-2'-nitroacetophenoneHCID 244025—
용매Methyl Ethyl KetoneHCID 6569—
생성물Ethyl 6-(2-nitrophenyl)imidazo[2,1-b]thiazole-3-carboxylateHCID 2523252279.4%

반응 단계

In a typical run, 2.1 g of ethyl 2-aminothiazole-4-carboxylate (Combi-Blocks, 0.0123 mol) was mixed with 25 mL of methyl ethyl ketone along with 2-bromo-2′-nitroacetophenone (3.0 g, 0.0123 mol). The reaction mixture was stirred under reflux for 18 hours. It was then cooled to room temperature and filtered to remove some of the solids. The filtrate was concentrated to afford 3.10 g of 6-(2-nitro-phenyl)-imidazo[2,1-b]thiazole-3-carboxylic acid ethyl ester (MS, M++H=318).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08088928B2
출처 데이터셋uspto-grants-2012_01
ORD IDord-f11f0e9818664a20991016afb4914dc7
출처 메모uspto-grants-2012_01