HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → N-[4-(5-Cyano-1-methyl-1H-pyrrol-2-yl)phenyl]furan-2-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Furancarbonyl chloride | HCID 68242 | — |
| Reactant | 5-(4-aminophenyl)-1-methyl-1H-pyrrole-2-carbonitrile | HCID 16050430 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | N-[4-(5-Cyano-1-methyl-1H-pyrrol-2-yl)phenyl]furan-2-carboxamide | HCID 16037459 | 28.1% |
Reaction Steps
5-(4-Aminophenyl)-1-methyl-1H-pyrrole-2-carbonitrile (98 mg, 0.5 mmol) was dissolved in dichloromethane (2 mL) and triethylamine (87 μL, 0.6 mmol) was added. Furan-2-carbonyl chloride (54 μL, 0.55 mmol) was added and the mixture was stirred 16 hours. The mixture was diluted with 50% ether in ethyl acetate and washed with water, saturated NaHCO3, 2N HCl, brine, dried over MgSO4, and passed through a plug of silica gel. The solution was concentrated to give N-[4-(5-cyano-1-methyl-1H-pyrrol-2-yl)phenyl]-2-furamide (0.041 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07297713B2 |
| Source dataset | uspto-grants-2007_11 |
| ORD ID | ord-5172d02ab78149a8b1d60aa6d4e01ded |
| Source note | uspto-grants-2007_11 |