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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

반응식

참여 물질

역할이름HCID투입량
반응물(1-Benzothiophen-3-yl)boronic acidHCID 2776344—
반응물5-Bromo-3-ureidothiophene-2-carboxamideHCID 21975855—
용매1,2-DimethoxyethaneHCID 8071—
생성물(Aminocarbonyl)amino-5-(1-benzothien-3-yl)thiophene-2-carboxamideHCID 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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07098240B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-798a65328c5e4ea19223cb360c86736d
출처 메모uspto-grants-2006_08