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HRID 1362371作成日:2026年10月25日

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

https://huagongshe.com/reaction/1362371

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 1852575345%

反応手順

1-Methyl-1H-indole-5-carbaldehyde (338 mg, 2.13 mmol) was dissolved in anhydrous methanol (10 ml). Methylamine (0.80 ml of 33% solution in ethanol, 6.43 mmol) was added and the reaction was stirred for 3 h. The solution was concentrated to a brown oil and then dissolved in anhydrous methanol (10 ml). Sodium borohydride (83.0 mg, 2.19 mmol) was added and the mixture was stirred overnight at room temperature. Water (4 ml) was added and the solution was concentrated. Sodium hydroxide (8 ml, 1N) was added and the aqueous layer was extracted with ethyl acetate (3×20 ml). Combined organic layers were dried over MgSO4, filtered and concentrated to afford methyl-(1-methyl-1H-indol-5-ylmethyl)-amine (167 mg, 45%) as an orange oil: 1H NMR (400 MHz, DMSO-d6) δ 7.44 (s, 1H), 7.34 (d, J=8.0 Hz, 1H), 7.261 (d, J=3.2 Hz, 1H), 7.11 (d, J=12.0 Hz, 1H), 6.345 (d, J=4.0 Hz, 1H), 3.75 (s, 3H), 3.70 (s, 2H), 2.25 (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-00c2ad85f56b4055a48316a99d331c20
出典メモuspto-grants-2011_02