Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2401436Generated: October 30, 2026

4-bromo-N-methoxy-N,1-dimethyl-1H-pyrazole-3-carboxamide → (4-bromo-1-methyl-1H-pyrazol-3-yl)(4-chlorophenyl)methanone

https://huagongshe.com/reaction/2401436

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-bromo-N-methoxy-N,1-dimethyl-1H-pyrazole-3-carboxamideHCID 86666729—
ReactantHCID 178478191HCID 178478191—
SolventTetrahydrofuranHCID 8028—
Product(4-bromo-1-methyl-1H-pyrazol-3-yl)(4-chlorophenyl)methanoneHCID 6781821084%

Reaction Steps

To a solution of compound 4-bromo-N-methoxy-N,1-dimethyl-1H-pyrazole-3-carboxamide (1.0 g, 4 mmol) in anhydrous tetrahydrofuran (20 mL) under nitrogen atmosphere was added (4-chlorophenyl)magnesium bromide (8 mL) in tetrahydrofuran (1 M) at 0° C., The resulting mixture was stirred for 2 h at room temperature. The reaction was quenched by saturated solution of ammonium chloride, and dichloromethane (100 mL) was added, the separated organic layer was dried over anhydrous sodium sulfate and concentrated in vacuum. The residue was purified by flash chromatography eluting with petroleum ether/ethyl acetate=5:1 to give the titled product as a white solid (1.0 g, 84%). LC/MS m/z 298 [M+H]+; 1H NMR (300 MHz, CDCl3) δ 8.10 (d, J=9 Hz, 2H), 7.53 (s, 1H), 7.43 (d, J=9 Hz, 2H), 3.99 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08796261B2
Source datasetuspto-grants-2014_08
ORD IDord-c71cac47280541ba980084ca1daa03fb
Source noteuspto-grants-2014_08