HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 5-bromo-1-phenyl-N,N-dimethyl-1H-pyrazole-4-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Dimethylamine, hydrochloride | HCID 10473 | — |
| Reactant | 1,1'-Carbonyldiimidazole | HCID 68263 | — |
| Reactant | 5-bromo-1-phenyl-1H-pyrazole-4-carboxylic acid | HCID 13821931 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 5-bromo-1-phenyl-N,N-dimethyl-1H-pyrazole-4-carboxamide | HCID 13821935 | 37% |
Reaction Steps
Three grams of 5-bromo-1-phenyl-1H-pyrazole-4-carboxylic acid and 2.6 g of carbonyldiimidazole was dissolved in 50 ml of DMF. The solution was stirred for 20 minutes and 2.3 g of triethylamine and 1.8 g of dimethylamine hydrochloride were added to the reaction mixture. The mixture was stirred at room temperature for 3 hours and was poured into ice water. The precipitated solid was collected by filtration and recrystallized from ethanol/water to afford 1.2 g of 5-bromo-1-phenyl-N,N-dimethyl-1H-pyrazole-4-carboxamide. Yield 37%. mp=79°-81° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04620865 |
| Source dataset | uspto-grants-1986_11 |
| ORD ID | ord-79b6b029435543b2a330c20b14ee2374 |
| Source note | uspto-grants-1986_11 |