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HRID 18227作成日:2026年10月26日

Methylamine → 1-Methyl-3-(methylaminomethyl)indole

https://huagongshe.com/reaction/18227

反応式

関与物質

役割名称HCID仕込み量
反応物MethylamineHCID 6329—
反応物1-Methyl-1H-indole-3-carbaldehydeHCID 87894—
反応物Sodium borohydrideHCID 4311764—
溶媒MethanolHCID 887—
生成物1-Methyl-3-(methylaminomethyl)indoleHCID 10986778—

反応手順

To a solution of 1-methylindole-3-carboxaldehyde (10.0 g, 62.8 mmole) in MeOH (100 mL) was added a solution of 2.0 M CH3NH2 in MeOH (126 mL, 252.0 mmole). The reaction was stirred at RT for 2 hrs, then was concentrated to a light yellow oil. This oil was dissolved in EtOH (300 mL), and NaBH4 (2.38 g, 62.8 mmole) was added. After 2 hrs the reaction was concentrated to a slurry and dissolved in 1.0 N NaOH (75 mL). The aqueous solution was extracted with Et2O (2×200 mL) and the combined organic fractions were dried over Na2SO4 and concentrated. Flash chromatography on silica gel (9:1 CHCl3/MeOH containing 5% NH4OH) and drying in high vacuum left the title compound (10.1 g, 92%) as a faintly yellow oil: 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-91ebed200773476eb1e380408676ffd3
出典メモuspto-grants-2010_06