HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetyl chloride → 3-Acetylaminopyrazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Pyrazol-3-ylamine | HCID 74561 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-Acetylaminopyrazole | HCID 2777527 | 79.7% |
Reaction Steps
To a solution of 1H-pyrazol-5-amine (50 g, 0.602 mol) and N-methylmorpholine (160 mL, 1.44 mol) in CH2Cl2 (2 L) was added acetyl chloride (99 mL, 1.38 mol) dropwise at 0° C. under an atmosphere of nitrogen. The reaction mixture was stirred at room temperature for 1 d. Some di-acylated product was observed in an LCMS. The reaction mixture was concentrated in vacuo and the resulting solid was suspended in MeOH (2 L) and cooled to 0° C. 4 M NaOH solution (aq., 440 mL, 1.75 mol) was added slowly and the mixture allowed to warm to room temperature over 1.5 h. The MeOH was removed in vacuo and the solid was collected by filtration, washed with minimal cold water and dried in vacuo to provide the title compound as a solid (60 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08765762B2 |
| Source dataset | uspto-grants-2014_07 |
| ORD ID | ord-0dc33b13b09642c4855cb7b3a4c60b3b |
| Source note | uspto-grants-2014_07 |