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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1355627생성일: 2026년 10월 27일

p-Anisoyl chloride → Ethyl 3-(4-methoxybenzamido)-1H-indole-2-carboxylate

https://huagongshe.com/reaction/1355627

반응식

참여 물질

역할이름HCID투입량
반응물p-Anisoyl chlorideHCID 7477—
반응물TriethylamineHCID 8471—
반응물Ethyl 3-amino-1H-indole-2-carboxylateHCID 732887—
용매DichloromethaneHCID 6344—
용매Ethyl AcetateHCID 8857—
생성물Ethyl 3-(4-methoxybenzamido)-1H-indole-2-carboxylateHCID 75136394.1%

반응 단계

To a solution of 3-amino-2-indolecarboxylic acid ethyl ester (500 mg, 2.45 mmol) and triethylamine (272 mg, 2.70 mmol) in methylene chloride (5 mL) was added anisoyl chloride (418 mg, 2.45 mmol). The resulting mixture was stirred for 18 h at room temperature. The reaction mixture was diluted with ethyl acetate and washed with water. The organic phase was washed with 1 N aqueous hydrochloric acid, dried (sodium sulfate), filtered, and concentrated in vacuo to provide a yellow solid. Recrystallization from hexane/ethyl acetate provided 780 mg (94%) of the title compound as a yellow solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06586459B2
출처 데이터셋uspto-grants-2003_07
ORD IDord-209c1c53411c4a919ad228597f1cc357
출처 메모uspto-grants-2003_07