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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 14600생성일: 2026년 10월 25일

Triethylamine → 4-[4-(2-Chloro-phenoxy)-butyrylamino]-thiophene-3-carboxylic acid methyl ester

https://huagongshe.com/reaction/14600

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Methyl 4-aminothiophene-3-carboxylate HydrochlorideHCID 2777609—
반응물4-(2-Chloro-phenoxy)-butyryl chlorideHCID 13721442—
용매DichloromethaneHCID 6344—
생성물4-[4-(2-Chloro-phenoxy)-butyrylamino]-thiophene-3-carboxylic acid methyl esterHCID 6868797880%

반응 단계

To 4-amino-thiophene-3-carboxylic acid methyl ester hydrochloride (199 mg, 0.994 mmol) in dichloromethane (1.9 mL) and triethylamine (0.29 mL, 2.08 mmol), was slowly added a crude solution of 4-(2-chloro-phenoxy)-butyryl chloride (271 mg, approximately 1.16 mmol) in dichloromethane (1.9 mL). The reaction mixture was stirred for 3 hours at room temperature. The reaction mixture was then further diluted with dichloromethane (50 mL) and washed with water. The aqueous phase was then extracted with dichloromethane and the combined organic phases were dried with sodium sulfate, and concentrated in vacuo. The residue was then purified by column chromatography (SiO2, Heptane/EtOAc: 0-80%) to yield the title compound as a white solid (281 mg, 80%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07732452B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-3cab4796b04140f4a3017521a6e9df0b
출처 메모uspto-grants-2010_06