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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 610143Generated: October 31, 2026

Triethylamine → 1-[(4-methoxy)phenyl]-3-(ethoxycarbonyl)-1H-pyrazole

https://huagongshe.com/reaction/610143

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1-[(4-Methoxy)phenyl]-3-(ethoxycarbonyl)pyrazole-5-carboxylic acidHCID 54476224—
SolventThionyl ChlorideHCID 24386—
Product1-[(4-methoxy)phenyl]-3-(ethoxycarbonyl)-1H-pyrazoleHCID 1437267091.5%

Reaction Steps

A solution of 1-[(4-methoxy)phenyl]-3-(ethoxycarbonyl)pyrazole-5-carboxylic acid (3.2 g, 11.1 mmol) in 20 mL of thionyl chloride was stirred at 80° C. for 1 h. The volatiles were then removed and the residue was azeotroped with 20 mL of toluene and dried in vacuo. The residue was dissolved in 50 mL of methylene chloride and then there was added triethylamine (4.6 mL, 33.3 mmol) and 4-(N-pyrrolidinocarbonyl)aniline (3.2 mL, 54.3 mmol). The reaction mixture was allowed to stir at ambient temperature for 4 h. The volatiles were removed and the residue was dissolved in ethyl acetate, washed sequentially with 10% aq HCl and brine, dried (MgSO4), filtered through a short pad of silica gel and concentrated to afford 2.5 g (50%) of the title compound. A small portion was further purified by prep HPLC (C18 reverse phase column, elution with a H2O/CH3CN gradient with 0.5% TFA) and lyophilized to afford the title compound as a white powder. LRMS (ES+): 463.1 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05998424
Source datasetuspto-grants-1999_12
ORD IDord-0d0fbd1750b349f8af68d0cf6fdf572e
Source noteuspto-grants-1999_12