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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2068476Generated: November 1, 2026

Ammonium Chloride → Methyl-[5-(4-chlorophenyl)-3-methyl-1-(pyrimidin-5-yl)-1h-pyrazol-4-yl]acetate

https://huagongshe.com/reaction/2068476

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantCesium fluorideHCID 25953—
Reactant(Pyrimidin-5-yl)boronic acidHCID 2795193—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 178499523HCID 178499523—
CatalystCupric acetateHCID 8895—
SolventDichloromethaneHCID 6344—
ProductMethyl-[5-(4-chlorophenyl)-3-methyl-1-(pyrimidin-5-yl)-1h-pyrazol-4-yl]acetateHCID 44538001—

Reaction Conditions

Temperature20 °C

Reaction Steps

0.287 g (2 mmol) of cesium fluoride, 0.103 g (1 mmol) of copper(II) acetate and 0.212 g (2 mmol) of potassium tert-butoxide 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. 0.234 g (2 mmol) of 5-pyrimidinylboronic acid was then added, and the mixture was stirred at 20° C. for 45 h. The mixture was then added to saturated ammonium chloride solution (10 ml) 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 0.040 g of product (5.8% of theory).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08298994B2
Source datasetuspto-grants-2012_10
ORD IDord-e5415bb0317048769b49d3787c39ea4c
Source noteuspto-grants-2012_10