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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1362440Generated: October 30, 2026

Water → (1,3-dimethyl-1H-indol-2-yl)-N-methylmethanamine

https://huagongshe.com/reaction/1362440

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantMethylamineHCID 6329—
Reactant1,3-dimethyl-1H-indole-2-carbaldehydeHCID 2771468—
ReactantSodium borohydrideHCID 4311764—
SolventMethanolHCID 887—
Product(1,3-dimethyl-1H-indol-2-yl)-N-methylmethanamineHCID 2213913185.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

Methylamine (0.53 mL, 13.1 mmol) was added to a solution of 1,3-dimethyl-1H indole-2-carbaldehyde (760 mg, 4.3 mmol) in methanol (15 mL) and stirred for 5 h. The mixture was cooled to 0° C. and sodium borohydride (159 mg, 4.3 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 (690 mg, 85%). 1H NMR (400 MHz, DMSO-d6) δ 7.44 (d, J=7.8 Hz, 1H), 7.34 (d, J=8.1 Hz, 1H), 7.10 (t, J=7.6 Hz, 1H), 6.98 (t, J=8.0 Hz, 1H), 3.77 (s, 2H), 3.71 (s, 3H), 2.27 (s, 3H), 2.23 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07879872B2
Source datasetuspto-grants-2011_02
ORD IDord-70f793f84e19442f9d15b4e71c43a06d
Source noteuspto-grants-2011_02