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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 530426Generated: October 31, 2026

3-Methylbenzoic acid → 2-{4-[(3-methylbenzoyl)amino]phenyl}-1H-indole-1-carboxamide

https://huagongshe.com/reaction/530426

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Methylbenzoic acidHCID 7418—
Reactant2-(4-Amino-phenyl)-indole-1-carboxylic acid amideHCID 121254621—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
Solvent1,2-DichloroethaneHCID 11—
SolventEthyl AcetateHCID 8857—
Product2-{4-[(3-methylbenzoyl)amino]phenyl}-1H-indole-1-carboxamideHCID 121254612—

Reaction Conditions

Temperature60 °C

Reaction Steps

To the solution of 2-(4-amino-phenyl)-indole-1-carboxylic acid amide (125.5 mg, 0.5 mmol, 1 eq) and m-toluic acid (68.8 mg, 0.5 mmol, 1 eq) in anhydrous DCE (4 mL) was added DMAP (12.2 mg, 0.2 eq) and EDC (115.2 mg, 1.2 eq). The reaction mixture was heated at 60° C. for 1.5 hours. It was then cooled to room temperature, diluted with ethyl acetate, washed subsequently with aqueous NH4Cl, saturated aqueous NaHCO3, brine, and lastly dried with anhydrous sodium sulfate. The upper liquor was decanted, concentrated, and the solid residue was treated with EtOAC-Hex(2:1) with stirring. 2-{4-[(3-methylbenzoyl)amino]phenyl}-1H-indole-1-carboxamide was obtained as slightly brown solid upon filtration in amount of 165 mg (89%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09353093B2
Source datasetuspto-grants-2016_05
ORD IDord-16d4b60122aa4291ae9c590161643a9d
Source noteuspto-grants-2016_05