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HRID 428020作成日:2026年10月27日

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

https://huagongshe.com/reaction/428020

反応式

関与物質

役割名称HCID仕込み量
反応物p-Anisoyl chlorideHCID 7477—
反応物TriethylamineHCID 8471—
反応物Ethyl 3-amino-1H-indole-2-carboxylateHCID 732887—
溶媒DichloromethaneHCID 6344—
溶媒Ethyl AcetateHCID 8857—
生成物Ethyl 3-(4-methoxybenzamido)-1H-indole-2-carboxylateHCID 75136394.1%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06313151B1
出典データセットuspto-grants-2001_11
ORD IDord-733b89533ee64034b26e3ebb33f90f79
出典メモuspto-grants-2001_11