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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 225836Generated: October 26, 2026

Methylamine → N,1-dimethylindole-2-carboxamide

https://huagongshe.com/reaction/225836

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylamineHCID 6329—
Reactantethyl 1-methyl-1H-indole-2-carboxylateHCID 143368—
SolventMethanolHCID 887—
ProductN,1-dimethylindole-2-carboxamideHCID 12303315—

Reaction Steps

A suspension of ethyl 1-methyl-1H-indole-2-carboxylate (27.10 g, 133.34 mmole) in 40% aqueous CH3NH2 (300 mL) and MeOH (30 mL) was stirred at RT. A solid tended to gradually creep up the walls of the flask, and was washed down periodically with MeOH. The flask was tightly stoppered to keep the material inside the flask. As the reaction proceeded, the solid dissolved, but eventually the product began to precipitate. The reaction was stirred at RT for 5 days, then was concentrated to remove approximately 200 mL of the solvent. The remaining residue was diluted with H2O (300 mL), and the solid was collected by suction filtration and washed with H2O. Drying at 50-60° C. in high vacuum left the title compound (23.45 g, 93%) as a faintly yellow solid: 1H NMR (300 MHz, CDCl3) δ 7.63 (d, J=8.0 Hz, 1 H), 7.27-7.43 (m, 2 H), 7.10-7.20 (m, 1 H), 6.80 (s, 1 H), 6.10-6.30 (m, 1 H), 4.06 (s, 3 H), 3.01 (d, J=4.9 Hz, 3 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07557125B2
Source datasetuspto-grants-2009_07
ORD IDord-0742e915f964432391dc267e2798bd7f
Source noteuspto-grants-2009_07