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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1952726Generated: November 4, 2026

Triethylamine → N-Methoxy-N-methyl-1H-indole-3-carboxamide

https://huagongshe.com/reaction/1952726

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
ReactantIndole-3-Carboxylic AcidHCID 69867—
ReactantMethanamine, N-methoxy-, hydrochloride (1:1)HCID 81138—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductN-Methoxy-N-methyl-1H-indole-3-carboxamideHCID 2329958978%

Reaction Steps

Indole-3-carboxylic acid (2.50 g, 0.0155 mol) was suspended in dichloromethane (60 ml) and treated with oxalyl chloride (1.62 ml, 0.0186 mol), followed by a drop of dry DMF. The reaction mixture was then stirred at room temperature overnight, before being evaporated under reduced pressure and dried in vacuo. The product was then redissolved in dichloromethane (50 ml) and added slowly to a solution of N,O-dimethylhydroxylamine hydrochloride (1.59 g, 0.0163 mol) in dichloromethane (50 ml) containing triethylamine (4.53 ml, 0.0326 mol) under argon. The resultant mixture was then stirred at room temperature for 2 h, before being washed with water, followed by aq. NaHCO3. The organic layer was then dried (Na2SO4), evaporated under reduced pressure and dried in vacuo to yield the title compound as white solid (2.46 g, 78%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06114329
Source datasetuspto-grants-2000_09
ORD IDord-fa2d91cd8e7f41ff8cae7dff4cd848fe
Source noteuspto-grants-2000_09