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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 889228생성일: 2026년 10월 24일

4-Ethoxyphenylthiourea → N-(4-Ethoxyphenyl)-4-(6-methylimidazo[2,1-b][1,3]thiazol-5-yl)-1,3-thiazol-2-amine;hydrobromide

https://huagongshe.com/ko/reaction/889228

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참여 물질

역할이름HCID투입량
반응물4-EthoxyphenylthioureaHCID 853569—
반응물2-Bromo-1-(6-methylimidazo[2,1-b]thiazol-5-yl)ethanone hydrobromideHCID 86627848—
용매EthanolHCID 702—
생성물N-(4-Ethoxyphenyl)-4-(6-methylimidazo[2,1-b][1,3]thiazol-5-yl)-1,3-thiazol-2-amine;hydrobromideHCID 2877568—

반응 단계

A mixture of 2-bromo-1-(6-methylimidazo[2,1-b]thiazol-5-yl)ethanone hydrobromide (18) (2.20 g, 6.5 mmol) and (p-ethoxyphenyl)thiourea (10) (1.30 g, 6.5 mmol) in 40 mL of anhydrous ethanol was refluxed under stirring for 20 h, and then cooled to room temperature. The solid was filtered. The crude white solid product was re-crystallized from methanol. The methanol solution was filtered while still hot to remove possible dust, and then heated into solution. It was re-crystallized two more times from methanol, and dried under vacuum to provide the desired product 20 as a white solid, yield 0.64 g (22.4%), HPLC purity 97.81%, mp >240° C. 1HNMR (CD3OD) δ 1.27 (t, 3H, J=6.8 Hz), 2.56 (s, 3H), 3.88-3.94 (m, 2H), 6.85 (d, 2H, J=8.8 Hz), 6.97 (s, 1H), 7.34 (d, 2H, J=8.8 Hz), 7.54 (d, 1H, J=4.4 Hz), 8.44 (d, 1H, J=4.4 Hz). ESI-MS m/z 357 (M+1)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08252822B2
출처 데이터셋uspto-grants-2012_08
ORD IDord-20895cacf9754a578ed0cb7f679b5719
출처 메모uspto-grants-2012_08