Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 362793Generated: November 1, 2026

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

https://huagongshe.com/reaction/362793

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 2h, 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 numberUS05872134
Source datasetuspto-grants-1999_02
ORD IDord-92f9fbce7d014f958801abf31ee7f2c4
Source noteuspto-grants-1999_02