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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 8124생성일: 2026년 10월 23일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물DimethylamineHCID 674—
반응물MethanolHCID 887—
반응물methyl 3-formyl-1H-indole-6-carboxylateHCID 735867—
반응물Sodium borohydrideHCID 4311764—
용매ChloroformHCID 6212—
용매Sodium chloride; waterHCID 57417360—
생성물Ammonia methanolHCID 2170589720%
생성물3-dimethylamino-methyl-1H-indole-6-carboxylic acid methyl esterHCID 6951645499%

반응 조건

온도55 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07087635B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-3dd918785d8c438daa628a564fa5be31
출처 메모uspto-grants-2006_08