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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1362371생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/1362371

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물MethylamineHCID 6329—
반응물Sodium borohydrideHCID 4311764—
반응물1-methyl-1H-indole-5-carbaldehydeHCID 7537534—
용매MethanolHCID 887—
생성물n-Methyl-1-(1-methyl-1h-indol-5-yl)methanamineHCID 1852575345%

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07879872B2
출처 데이터셋uspto-grants-2011_02
ORD IDord-00c2ad85f56b4055a48316a99d331c20
출처 메모uspto-grants-2011_02