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HRID 18228作成日:2026年10月26日

Methylamine → N-Methyl-N-[(2-methyl-1H-indol-3-yl)methyl]amine

https://huagongshe.com/reaction/18228

反応式

関与物質

役割名称HCID仕込み量
反応物MethylamineHCID 6329—
反応物3-Formyl-2-methylindoleHCID 73166—
反応物Sodium borohydrideHCID 4311764—
溶媒MethanolHCID 887—
生成物N-Methyl-N-[(2-methyl-1H-indol-3-yl)methyl]amineHCID 1095402363%

反応手順

To a solution of 2-methylindole-3-carboxaldehyde (10.00 g, 62.84 mmole) in MeOH (100 mL) was added 2 M CH3NH2 in MeOH (200 mL). After stirring for 3 hours at RT, the reaction solution was concentrated to a yellow oil which solidified under vacuum. This solid was dissolved in ethanol (350 mL) and NaBH4 (2.38 g, 62.8 mmole) was added. The reaction was stirred at RT for 6 hours, then was concentrated under vacuum. The remaining residue was diluted with saturated aqueous Na2CO3 (50 mL) and extracted with EtOAc (2×200 mL). The organic phase was separated, washed with brine, and dried over Na2SO4. Flash chromatography on silica gel (9:1 CHCl3/MeOH containing 5% NH4OH) and drying under high vacuum gave the title compound (6.88 g, 63%) as a faintly yellow viscous solid: MS (ES) m/e 175 (M+H)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07741339B2
出典データセットuspto-grants-2010_06
ORD IDord-53d950d90541411399039216f0d61e5c
出典メモuspto-grants-2010_06