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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3-Methylbenzoic acid | HCID 7418 | — |
| Reactant | 2-(4-Amino-phenyl)-indole-1-carboxylic acid amide | HCID 121254621 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2-{4-[(3-methylbenzoyl)amino]phenyl}-1H-indole-1-carboxamide | HCID 121254612 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09353093B2 |
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| Source dataset | uspto-grants-2016_05 |
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| ORD ID | ord-16d4b60122aa4291ae9c590161643a9d |
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| Source note | uspto-grants-2016_05 |
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