Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2205758Generated: November 3, 2026

Acetyl chloride → 3-Acetylaminopyrazole

https://huagongshe.com/reaction/2205758

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
Reactant4-MethylmorpholineHCID 7972—
ReactantSodium HydroxideHCID 14798—
ReactantPyrazol-3-ylamineHCID 74561—
SolventDichloromethaneHCID 6344—
Product3-AcetylaminopyrazoleHCID 277752779.7%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09371332B2
Source datasetuspto-grants-2016_06
ORD IDord-9ec5f41752d848a9b9d8d94217ee8533
Source noteuspto-grants-2016_06