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HRID 2393205作成日:2026年10月27日

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

https://huagongshe.com/reaction/2393205

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Ethyl chloroformateHCID 10928—
反応物Ammonium ChlorideHCID 25517—
反応物4-Oxo-4,5,6,7-tetrahydro-1H-indole-3-carboxylic acidHCID 15337632—
反応物N-trifluoroacetyl-(methylaminomethyl)anilineHCID 57112434—
溶媒DimethylformamideHCID 6228—
生成物N-[3-(methylaminomethyl)phenyl]-4-oxo-4,5,6,7-tetrahydro-1H-indole-3-carboxamideHCID 9817695—

反応手順

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. m.p. 130°-132° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05804686
出典データセットuspto-grants-1998_09
ORD IDord-91f8aacda88f4d0c9bbc5446b79c648e
出典メモuspto-grants-1998_09