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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1094975생성일: 2026년 10월 27일

Pyridine → 2-(3-Chloromethyl-benzoylamino)-4,5,6,7-tetrahydro-benzo[b]thiophene-3-carboxylic acid ethyl ester

https://huagongshe.com/reaction/1094975

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물DichloromethaneHCID 6344—
반응물Veratroyl chlorideHCID 77070—
반응물Ethyl 2-amino-4,5,6,7-tetrahydrobenzo[b]thiophene-3-carboxylateHCID 78262—
생성물2-(3-Chloromethyl-benzoylamino)-4,5,6,7-tetrahydro-benzo[b]thiophene-3-carboxylic acid ethyl esterHCID 66639201—

반응 조건

온도0 °C

반응 단계

2-Amino-4,5,6,7-tetrahydrobenzothiophene-3-carboxylic acid ethyl ester (Compound A) (4.0 g) was dissolved in anhydrous methylene chloride (40.0 ml). Subsequently, pyridine (2.8 ml) and 3-(chloromethyl)benzoyl chloride (compound B) (3.0 ml) were added at 0° C., and the mixture was stirred at 0° C. for one hr. After the completion of the reaction, distilled water was added, and the mixture was subjected to separatory extraction with chloroform, and the organic layer was washed with saturated brine, was dried over sodium sulfate, and was then concentrated to give 2-(3-chloromethyl-benzoylamino)-4,5,6,7-tetrahydro-benzo[b]thiophene-3-carboxylic acid ethyl ester as a useful intermediate (7.42 g, yield 100%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08134015B2
출처 데이터셋uspto-grants-2012_03
ORD IDord-d039a63894f94c38830b00a29956f7a9
출처 메모uspto-grants-2012_03