HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 90010296, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-Methylbenzoyl Chloride | HCID 13405 | — |
| Reactant | 1-Amino-1H-pyrrole-2-carboxamide | HCID 10419180 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 90010296 | HCID 90010296 | — |
Reaction Steps
Triethylamine (277 μl, 2.00 mmol) is added to a suspension of 1-amino-1H-pyrrole-2-carboxylic acid amide (250 mg, 2.00 mmol) in acetonitrile (4.0 ml). Under external cooling with ice, a solution of 4-methylbenzoyl chloride (264 μl, 2.00 mmol) in dichloromethane (0.6 ml) is added dropwise. The reaction mixture is stirred at room temperature for 18 hours. The solvents are evaporated and the residue is taken up in dichloromethane and saturated NaHCO3 solution. A precipitate forms which is filtered off, washed with water and dried under vacuum to give 1-(4-methyl-benzoylamino)-1H-pyrrole-2-carboxylic acid amide as white crystals; HPLC/MS 1.57 min (A), [M+H] 244;
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09174995B2 |
| Source dataset | uspto-grants-2015_11 |
| ORD ID | ord-f1216a01c70a4225a9af985f430cc83e |
| Source note | uspto-grants-2015_11 |