HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 5-bromo-1-phenyl-N-methoxy-1H-pyrazole-4-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1,1'-Carbonyldiimidazole | HCID 68263 | — |
| Reactant | O-Methylhydroxylamine hydrochloride | HCID 521874 | — |
| Reactant | 5-bromo-1-phenyl-1H-pyrazole-4-carboxylic acid | HCID 13821931 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 5-bromo-1-phenyl-N-methoxy-1H-pyrazole-4-carboxamide | HCID 13821937 | 34.7% |
Reaction Steps
A solution of 2.6 g of 5-bromo-1-phenyl-1H-pyrazole-4-carboxylic acid and 2.4 g of carbonyldiimidazole in 60 ml DMF was stirred at room temperature for 30 minutes. Two grams of triethylamine and 1.7 g of methoxyamine hydrochloride were added to the solution. The mixture was stirred at room temperature for 24 hours and another equivalent of triethylamine and methoxyamine hydrochloride were added. The mixture was heated on the steam bath for two hours and poured into ice water. The precipitated solid was collected by filtration and recrystallized from ethanol to afford 1.0 g of 5-bromo-1-phenyl-N-methoxy-1H-pyrazole-4-carboxamide. Yield 34%. mp=194°-197° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04620865 |
| Source dataset | uspto-grants-1986_11 |
| ORD ID | ord-3906111bfe2e4b93aa1819dcdad19618 |
| Source note | uspto-grants-1986_11 |