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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2068477Generated: October 30, 2026

Hydrochloric Acid → Methyl-[5-(4-chlorophenyl)-1-(2-chloropyrimidin-5-yl)-3-methyl-1h-pyrazol-4-yl]acetate

https://huagongshe.com/reaction/2068477

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPyridineHCID 1049—
Reactant(2-Chloropyrimidin-5-yl)boronic acidHCID 21747362—
ReactantHCID 178499523HCID 178499523—
CatalystCupric acetateHCID 8895—
SolventDichloromethaneHCID 6344—
ProductMethyl-[5-(4-chlorophenyl)-1-(2-chloropyrimidin-5-yl)-3-methyl-1h-pyrazol-4-yl]acetateHCID 131730040—

Reaction Conditions

Temperature20 °C

Reaction Steps

0.515 g (3 mmol) of copper(II) acetate and 0.306 ml (4 mmol) of pyridine were added to 0.5 g (2 mmol) of methyl[5-(4-chlorophenyl)-3-methyl-1H-pyrazol-4-yl]acetate in 10 ml of dichloromethane. 0.598 g (4 mmol) of 2-chloropyrimidine-5-boronic acid was then added, and the mixture was stirred at 20° C. for 24 h. The mixture was then added to 1 M HCl and extracted with dichloromethane. The combined organic phases were dried with magnesium sulfate, filtered and concentrated. The crude product was purified by preparative HPLC. This gave 0.015 g of product (2% of theory).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08298994B2
Source datasetuspto-grants-2012_10
ORD IDord-4ed2d21a9a9a4924bbec920782b89eb6
Source noteuspto-grants-2012_10