Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 11426생성일: 2026년 10월 25일
(1-Benzothiophen-3-yl)boronic acid → (Aminocarbonyl)amino-5-(1-benzothien-3-yl)thiophene-2-carboxamide
https://huagongshe.com/reaction/11426
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | (1-Benzothiophen-3-yl)boronic acid | HCID 2776344 | — |
| 반응물 | 5-Bromo-3-ureidothiophene-2-carboxamide | HCID 21975855 | — |
| 용매 | 1,2-Dimethoxyethane | HCID 8071 | — |
| 생성물 | (Aminocarbonyl)amino-5-(1-benzothien-3-yl)thiophene-2-carboxamide | HCID 9836627 | — |
반응 단계
3-[(Aminocarbonyl)amino-5-bromothiophene-2-carboxamide (0.222 g) and 1-benzothien-3-ylboronic acid (0.449 g) were sonicated in 1,2-dimethoxyethane (15 ml) and saturated aqueous sodium hydrogen carbonate solution (3.5 ml) and purged with argon. Tetrakis(triphenylphosphine)-palladium (95 mg) was added and the mixture was heated at reflux with stirring for 4.5 h, then allowed to cool and stirred at room temperature overnight. The solution was filtered and washed through with 1,2-dimethoxyethane and water. The filtrate was concentrated in vacuo and taken up in dichloromethane (20 ml) and saturated aqueous sodium hydrogen carbonate solution (20 ml). The solid product was collected by filtration, washed with dichloromethane, water, diethyl ether and dried (226 mg).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07098240B2 |
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| 출처 데이터셋 | uspto-grants-2006_08 |
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| ORD ID | ord-798a65328c5e4ea19223cb360c86736d |
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| 출처 메모 | uspto-grants-2006_08 |
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