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HRID 8124作成日:2026年10月23日

Dimethylamine → 3-dimethylamino-methyl-1H-indole-6-carboxylic acid methyl ester

https://huagongshe.com/ja/reaction/8124

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylamineHCID 674—
反応物MethanolHCID 887—
反応物methyl 3-formyl-1H-indole-6-carboxylateHCID 735867—
反応物Sodium borohydrideHCID 4311764—
溶媒ChloroformHCID 6212—
溶媒Sodium chloride; waterHCID 57417360—
生成物Ammonia methanolHCID 2170589720%
生成物3-dimethylamino-methyl-1H-indole-6-carboxylic acid methyl esterHCID 6951645499%

反応条件

温度55 °C

反応手順

A solution of methyl 3-formylindole-6-carboxylate (8.0 g, 39.3 mmol) in 270 ml methanol is treated with dimethylamine (40% aqueous; 267 ml, 2.56 mol) at ambient temperature. After 45 minutes, NaBH4 (4.45 g, 118.1 mmol) is added, and the resulting mixture is heated at 55° C. for 3 hours. The reaction mixture is allowed to cool then is diluted with CHCl3 (200 ml) and brine (I 50 ml). The organic layer is washed with brine, dried over Na2SO4 and concentrated in vacuo. The crude residue is purified by flash chromatography (SiO2; 100% ethyl acetate then 20% 2M NH3/methanol in CHCl3) to give 9.07 g of 3-dimethylamino-methyl-1H-indole-6-carboxylic acid methyl ester(99%). Amine 61 is prepared from 3-dimethylaminomethyl-1H-indole-6-carboxylic acid methyl ester by essentially following the procedures detailed in Amine 49, 1 paragraph; and Amine 51, 3rd paragraph.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07087635B2
出典データセットuspto-grants-2006_08
ORD IDord-3dd918785d8c438daa628a564fa5be31
出典メモuspto-grants-2006_08