HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 4-iodo-1-methyl-1H-pyrazole-5-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 1,1'-Carbonyldiimidazole | HCID 68263 | — |
| Reactant | 4-Iodo-1-methyl-1H-pyrazole-5-carboxylic acid | HCID 673687 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-iodo-1-methyl-1H-pyrazole-5-carboxamide | HCID 3753008 | 75% |
Reaction Steps
A round-bottom flash was charged with 4-iodo-1-methyl-1H-pyrazole-5-carboxylic acid (297 g, 1.18 mol), DCM (2.97 L), and 1,1′-carbonyldiimidazole (CDI) (207 g, 97% by mass, 1.24 mol). The reaction mixture was stirred at room temperature for 45 min. Ammonium chloride (189 g, 3.53 mol) and triethylamine (498 mL, 3.53 mol) were added and the reaction mixture was stirred at room temperature overnight. The reaction mixture was concentrated in vacuo and the residue was suspended in H2O (˜3 L) and granulated at room temperature for 1 h. The solid was collected via filtration, washed with H2O, and dried in a vacuum oven to afford 4-iodo-1-methyl-1H-pyrazole-5-carboxamide as a colorless solid (222 g, 75% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09227956B2 |
| Source dataset | uspto-grants-2016_01 |
| ORD ID | ord-e3bcfb06889648cbaad8ed66c541d6c7 |
| Source note | uspto-grants-2016_01 |