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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1362446Generated: October 30, 2026

Water → (7-Ethyl-3-methyl-1h-indol-2-yl)-n-methanamine

https://huagongshe.com/reaction/1362446

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantMethylamineHCID 6329—
ReactantSodium borohydrideHCID 4311764—
Reactant7-ethyl-3-methyl-1H-indole-2-carbaldehydeHCID 59277564—
SolventMethanolHCID 887—
Product(7-Ethyl-3-methyl-1h-indol-2-yl)-n-methanamineHCID 6696721375.6%

Reaction Conditions

Temperature0 °C

Reaction Steps

Methylamine (0.7 mL, 17.6 mmol) was added to a solution of 7-ethyl-3-methyl-1H-indole-2-carbaldehyde (1.1 mg, 5.8 mmol) in methanol (5 mL) and stirred for 5 h. The mixture was cooled to 0° C. and sodium borohydride (218 mg, 5.8 mmol) added slowly. The mixture was warmed to rt and stirred overnight. Water (3 mL) was added slowly at 0° C. and evaporated to a paste. Water was added and the mixture extracted with dichloromethane. The organic phase was washed with water, dried and evaporated to afford the title compound (826 mg, 75%). 1H NMR (400 MHz, CDCl3) δ 8.22 (s, 1H), 7.34 (d, J=7.7 Hz, 1H), 7.01 (t, J=7.6 Hz, 1H), 6.96 (d, J=6.8 Hz, 1H), 3.87 (s, 2H), 2.79 (q, J=7.5 Hz, 2H), 2.45 (s, 3H), 2.24 (s, 3H), 1.31 (t, J=7.6 Hz, 3H)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07879872B2
Source datasetuspto-grants-2011_02
ORD IDord-bd7c56b71b6948728a3eb68fe270bda5
Source noteuspto-grants-2011_02