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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1395894생성일: 2026년 10월 27일

Benzoyl chloride → 3-(4-benzoylamino-phenylmethyl)-1-methyl-1H-indole-5-carboxylic acid methyl ester

https://huagongshe.com/reaction/1395894

반응식

참여 물질

역할이름HCID투입량
반응물Benzoyl chlorideHCID 7412—
반응물TetrahydrofuranHCID 8028—
반응물DiisopropylethylamineHCID 81531—
반응물3-(4-amino-benzyl)-1-methyl-1H-indole-5-carboxylic acid methyl esterHCID 69447499—
용매Diethyl EtherHCID 3283—
용매Ethyl AcetateHCID 8857—
생성물3-(4-benzoylamino-phenylmethyl)-1-methyl-1H-indole-5-carboxylic acid methyl esterHCID 6945303783%

반응 단계

A solution of 3-(4-amino-phenylmethyl)-1-methyl-1H-indole-5-carboxylic acid methyl ester (62 mg, 0.21 mmol), DIPEA (0.06 mL, 0.32 mmol), benzoyl chloride (0.03 mL, 0.23 mmol) and THF (5 mL) was stirred for 10 hr at room temperature. The solution was then diluted with ether (20 mL) and ethyl acetate (20 mL) and washed with aq. NaHCO3 (50 mL). The organic layer was dried over MgSO4, filtered and concentrated. The remaining residue was subjected to flash chromatography (ethyl acetate/hexane, 2:3) to provide 3-(4-benzoylamino-phenylmethyl)-1-methyl-1H-indole-5-carboxylic acid methyl ester (69 mg, 83% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08900565B2
출처 데이터셋uspto-grants-2014_12
ORD IDord-6be7b1bf62cf47f2a2bab87b6ed634c7
출처 메모uspto-grants-2014_12