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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2119436Generated: November 2, 2026

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

https://huagongshe.com/reaction/2119436

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 solutionof 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 numberUS06686368B1
Source datasetuspto-grants-2004_02
ORD IDord-6529c16faaac4e85a1b701d291a54a9f
Source noteuspto-grants-2004_02