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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | 4-Ethoxyphenylthiourea | HCID 853569 | — |
| 반응물 | 2-Bromo-1-(6-methylimidazo[2,1-b]thiazol-5-yl)ethanone hydrobromide | HCID 86627848 | — |
| 용매 | Ethanol | HCID 702 | — |
| 생성물 | N-(4-Ethoxyphenyl)-4-(6-methylimidazo[2,1-b][1,3]thiazol-5-yl)-1,3-thiazol-2-amine;hydrobromide | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08252822B2 |
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| 출처 데이터셋 | uspto-grants-2012_08 |
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| ORD ID | ord-20895cacf9754a578ed0cb7f679b5719 |
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| 출처 메모 | uspto-grants-2012_08 |
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