HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → HCID 22622781, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 2-Aminobiphenyl | HCID 7015 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | HCID 22622778 | HCID 22622778 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 22622781 | HCID 22622781 | — |
Reaction Steps
A solution of 1,5-dimethyl-4-trifluoromethylpyrrol-3-carboxylic acid (1.9 g) and oxalyl chloride (0.9 ml) in methylene chloride (20 ml) is stirred at room temperature in the presence of a catalytic amount of DMF. The solvent is evaporated under reduced pressure to give a crystalline solid. This solid is dissolved in methylene chloride (1 ml) and added to a solution of 2-biphenylamine (1.7 g) and triethylamine (4.2 ml) in methylene chloride (20 ml) at 0° C. The reaction mixture is stirred at room temperature for 2 hours. Evaporation of the solvent under reduced pressure, addition of water and filtering gives the N-(2-biphenylyl)-1,5-dimethyl-4-trifluoromethylpyrrol-3-carboxamide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06365620B2 |
| Source dataset | uspto-grants-2002_04 |
| ORD ID | ord-faf7e4e0618943a38ff9b169c22b396f |
| Source note | uspto-grants-2002_04 |