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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 906117Generated: October 31, 2026

Trifluoroacetic acid → 7-(aminocarbonyl)-1H-indole-4-carboxylic acid

https://huagongshe.com/reaction/906117

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactanttert-butyl 7-carbamoyl-1H-indole-4-carboxylateHCID 67404011—
SolventDichloromethaneHCID 6344—
Product7-(aminocarbonyl)-1H-indole-4-carboxylic acidHCID 57748333135.1%

Reaction Steps

4: To a solution of tert-butyl 7-carbamoyl-1H-indole-4-carboxylate (0.15 g, 0.58 mmol) in dichloromethane (10 mL) was added trifluoroacetic acid (10 mL), and the mixture was heated to reflux until the starting material was fully consumed. The solvent was evaporated followed by rotary evaporation of the residue from a mixture of ethyl acetate (50 mL) and toluene (50 mL). The procedure was repeated three times and the residue dried in vacuo to obtain 7-(aminocarbonyl)-1H-indole-4-carboxylic acid (0.16 g, 89%). MS (EI) for C10H8N2O3: 205 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08012956B2
Source datasetuspto-grants-2011_09
ORD IDord-c0f20ce342dc47d8a2a5124a0174d299
Source noteuspto-grants-2011_09