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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 322632생성일: 2026년 10월 26일

Triethylamine → N-[3-(methylaminomethyl)phenyl]-4-oxo-4,5,6,7-tetrahydro-1H-indole-3-carboxamide

https://huagongshe.com/reaction/322632

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Ethyl chloroformateHCID 10928—
반응물Ammonium ChlorideHCID 25517—
반응물4-Oxo-4,5,6,7-tetrahydro-1H-indole-3-carboxylic acidHCID 15337632—
반응물N-trifluoroacetyl-(methylaminomethyl)anilineHCID 57112434—
용매DimethylformamideHCID 6228—
생성물N-[3-(methylaminomethyl)phenyl]-4-oxo-4,5,6,7-tetrahydro-1H-indole-3-carboxamideHCID 9817695—

반응 단계

To a stirred solution of 4-oxo-4,5,6,7-tetrahydro-1H-indole-3-carboxylic acid (100 mg, 0.6 mmol) and triethylamine (0.15 mL, 1.1 mmol) in N,N-dimethylformamide (5 mL) at 0° C. is added ethyl chloroformate (0.1 mL, 1.1 mmol). After stirring an additional 1 hour, 3-(N-trifluoroacetyl-(methylaminomethyl)aniline (0.3 g, 1.3 mmol) is added. The reaction mixture is stirrred for 4 hours, then poured into saturated aqueous ammonium chloride and extracted 2× with ethyl acetate. The combined organic layers are washed sequentially with brine, aqueous 2N hydrochloric acid, then brine, dried over sodium sulfate, filtered, and concentrated in vacuo. To the residue is added 15% aqueous potassium bicarbonate (5 mL) and methyl alcohol (3 mL), then heated at reflux for 3 hours. After cooling, the reaction mixture is extracted with ethyl acetate, the organic layer dried over sodium sulfate, filtered, and concentrated in vacuo to give N-[3-(methylaminomethyl)phenyl]-4-oxo-4,5,6,7-tetrahydro-1H-indole-3-carboxamide; (Compound 1) m.p. 130-132° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06211365B1
출처 데이터셋uspto-grants-2001_04
ORD IDord-0ac1bd3ce1754b51b29a66257c0cdbf1
출처 메모uspto-grants-2001_04