Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1392233Generated: October 25, 2026

Ammonia → 5-trifluoromethoxy-1H-indole-2-carboxylic acid amide

https://huagongshe.com/reaction/1392233

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantOxalyl chlorideHCID 65578—
Reactant5-(Trifluoromethoxy)-1H-indole-2-carboxylic acidHCID 2777290—
SolventDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
Product5-trifluoromethoxy-1H-indole-2-carboxylic acid amideHCID 69220468—

Reaction Conditions

Temperature2.5 °C

Reaction Steps

Oxalyl chloride (2.63 ml, 30.6 mmol) was added dropwise at 0° C. within 45 min. to a suspension of 5-trifluoromethoxy-1H-indole-2-carboxylic acid (5 g, 20.4 mmol) in THF (20 ml) and N,N-dimethyl formamide (0.5 ml). Stirring was continued at 0-5° C. for 30 min. and thereafter for 3 h at room temperature. The resulting solution was cooled to 0-5° C. again and then added within 15 min. to 75 ml of a 25% aqueous solution of ammonia. After stirring for 30 min. the precipitated amide was collected, washed with water and dried at 40° C. in vacuo yielding 5-trifluoromethoxy-1H-indole-2-carboxylic acid amide as off white solid. Yield 5 g (100%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07342030B2
Source datasetuspto-grants-2008_03
ORD IDord-1dacd341192f45c2af9a533f0eb0a81b
Source noteuspto-grants-2008_03