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HRID 1362046作成日:2026年10月26日

Water → n-Methyl-1-(1-methyl-1h-indol-5-yl)methanamine

https://huagongshe.com/reaction/1362046

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物MethylamineHCID 6329—
反応物Sodium borohydrideHCID 4311764—
反応物1-methyl-1H-indole-5-carbaldehydeHCID 7537534—
溶媒MethanolHCID 887—
生成物n-Methyl-1-(1-methyl-1h-indol-5-yl)methanamineHCID 18525753100%

反応手順

N-Methylindole-5-carbaldehyde (800 mg, 5.1 mmol) was dissolved in anhydrous methanol (15 mL). Methylamine (7.15 mL of 2M solution in methanol, 15.3 mmol) was added and the reaction was stirred for 3 hr. The solution was concentrated to a yellow oil and then dissolved into anhydrous methanol (15 mL). Sodium borohydride (194 mg, 5.1 mmol) was added and the mixture was stirred overnight. Water (1 mL) was added and the solution was concentrated to an orange oil. Sodium hydroxide (5 mL, 1N) was added and the product was extracted with ethyl acetate (3×20 mL), dried over MgSO4 and concentrated to afford the title compound as an orange oil (885 mg, 100%). 1H NMR (200 MHz, CDCl3) δ 7.57 (s, 1H), 7.35-7.11 (m, 3H), 6.51 (d, J=2.9 Hz, 1H), 3.85 (s, 2H), 3.79 (s, 3H), 2.48 (s, 3H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07879872B2
出典データセットuspto-grants-2011_02
ORD IDord-6822850dad1b4f67aceff249dd8bc064
出典メモuspto-grants-2011_02