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HRID 1297364作成日:2026年10月25日

Methylamine → N-Methyl-1H-indole-3-methanamine

https://huagongshe.com/reaction/1297364

反応式

関与物質

役割名称HCID仕込み量
反応物MethylamineHCID 6329—
反応物Indole-3-CarboxaldehydeHCID 10256—
反応物Sodium borohydrideHCID 4311764—
溶媒MethanolHCID 887—
生成物N-Methyl-1H-indole-3-methanamineHCID 96388—

反応手順

To a solution of indole-3-carboxaldehyde (5.4 g, 34.1 mmole) in MeOH (30 mL) was added a solution of 2.0 M CH3NH2 in MeOH (51.3 mL, 102.6 mmole). The reaction was stirred at RT overnight, then was concentrated to a light yellow oil. This oil was dissolved in EtOH (40 mL), and NaBH4 (1.3 g, 34.1 mmole) was added. After 16 hrs the reaction was concentrated to a slurry and dissolved in 10% Na2CO3(100 mL). The aqueous solution was extracted with EtOAc (2×200 mL) and the combined organic fractions were dried over Na2SO4 and concentrated. Drying in high vacuum left the title compound (5.2 g, 94%) as a faintly yellow oil: MS (ES) m/e 161 (M+H)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07250424B2
出典データセットuspto-grants-2007_07
ORD IDord-7ff0402a46c5493aa972c6b7737ad95f
出典メモuspto-grants-2007_07