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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2085016Generated: October 31, 2026

Pyridine → ethyl 3-methyl-1-(2-naphthyl)-1H-pyrazole-5-carboxylate

https://huagongshe.com/reaction/2085016

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant(Naphthalen-2-yl)boronic acidHCID 2734375—
ReactantHCID 178469061HCID 178469061—
CatalystCupric acetateHCID 8895—
SolventDichloromethaneHCID 6344—
Productethyl 3-methyl-1-(2-naphthyl)-1H-pyrazole-5-carboxylateHCID 2272889170%

Reaction Steps

To the solution of 2-naphthylboronic acid (5.00 g, 29.1 mmol) and ethyl 3-methylpyrazole-5-carboxylate (4.48 g, 29.1 mmol) in 100 mL dry dichloromethane (DCM) were added pyridine (4.7 mL, 58.2 mmol) and anhydrous powder of copper(II) acetate (7.94 g, 43.7 mmol). Some activated molecular sieve powder was added afterwards. The resulting slurry was stirred for 2 days under argon. The mixture was diluted with DCM. It was filtered through a celite bed. The blue filtrate was washed with water (×2), dried over MgSO4, concentrated, purified by silica column to yield ethyl 3-methyl-1-(2-naphthyl)-1H-pyrazole-5-carboxylate and its regioisomer in a 1:1 ratio in 70% yield. Rf 0.59 (1:2 EtOAc: hexane), M+H 281; regioisomer, ethyl 5-methyl-1-(2-naphthyl)-1H-pyrazole-3-carboxylate, Rf 0.44 (1:2 EtOAc: hexane). ES-MS: (M+H)+ 281.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06720317B1
Source datasetuspto-grants-2004_04
ORD IDord-8a4df892e940405d9bebad0957ea06a0
Source noteuspto-grants-2004_04