Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2097178Generated: October 30, 2026

1,2-Dichloroethane → N-methyl-1H-indole-2-carboxamide

https://huagongshe.com/reaction/2097178

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantEthanolHCID 702—
ReactantMethylamineHCID 6329—
ReactantIndole-2-carboxylic acidHCID 72899—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantDiisopropylethylamineHCID 81531—
SolventTetrahydrofuranHCID 8028—
ProductN-methyl-1H-indole-2-carboxamideHCID 12461785153.8%

Reaction Steps

EDC (7.7 g, 40.3 mmol) was added to a solution of indole-2-carboxylic acid (5 g, 13.1 mmol), methylamine, 33% in ethanol (5.6 mL, 15.5 mmol), HOBT (4.1 g, 13.1 mmol) and DIPEA (2.1 mL, 12.4 mmol) in THF, anhydrous (45 mL) and stirred overnight. The crude mixture was evaporated in vacuo and chromatographed over silica eluting with methanol/dichloromethane (0-2%) to afford the title compound (3.51 g, 66%). 1H NMR (300 MHz, DMSO-d6) δ 11.53 (s, 1H), 8.43 (s, 1H), 7.57 (d, J=7.9 Hz, 1H), 7.39 (d, J=8.2 Hz, 1H), 7.15 (t, J=8.2 Hz, 1H), 7.03 (s, 1H), 6.98 (t, J=7.9 Hz, 1H), 2.79 (d, J=4.7 Hz, 3H)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08450307B2
Source datasetuspto-grants-2013_05
ORD IDord-2958db5450fd406caf446978c1751e33
Source noteuspto-grants-2013_05