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HRID 8124Erstellt: 23. Oktober 2026

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

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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethylamineHCID 674—
EduktMethanolHCID 887—
Eduktmethyl 3-formyl-1H-indole-6-carboxylateHCID 735867—
EduktSodium borohydrideHCID 4311764—
LösungsmittelChloroformHCID 6212—
LösungsmittelSodium chloride; waterHCID 57417360—
ProduktAmmonia methanolHCID 2170589720%
Produkt3-dimethylamino-methyl-1H-indole-6-carboxylic acid methyl esterHCID 6951645499%

Reaktionsbedingungen

Temperatur55 °C

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07087635B2
Quelldatensatzuspto-grants-2006_08
ORD IDord-3dd918785d8c438daa628a564fa5be31
Quellennotizuspto-grants-2006_08