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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 394804Generated: October 29, 2026

Triethylamine → 1-[(4-Methoxy)phenyl)-3-(methoxycarbonylamino)-5-(methoxycarbonyl)pyrazole

https://huagongshe.com/reaction/394804

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantSodium AzideHCID 33557—
ReactantIsobutyl chloroformateHCID 62365—
Reactant1-[(4-Methoxy)phenyl]-5-(methoxycarbonyl)pyrazole-3-carboxylic acidHCID 54210067—
SolventAcetoneHCID 180—
SolventEthyl AcetateHCID 8857—
Product1-[(4-Methoxy)phenyl)-3-(methoxycarbonylamino)-5-(methoxycarbonyl)pyrazoleHCID 5414987333.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 1-[(4-methoxy)phenyl]-5-(methoxycarbonyl)pyrazole-3-carboxylic acid (3.0 g, 10.9 mmol) in 50 mL of acetone at 0° C. was added triethylamine (1.66 mL, 11.9 mmol) followed by iso-butyl chloroformate (1.14 mL, 11.9 mmol). The resulting was stirred for 30 min whereupon an aqueous solution of sodium azide (2.82 g, 43.4 mmol) was added. The reaction was stirred at 0° C. for 1 h. The reaction was then diluted with ethyl acetate and washed with brine. The organics were dried (MgSO4) and concentrated in vacuo. The residue was dissolved in 50 mL of toluene and stirred at 100° C. for 1 h. The volatiles were removed in vacuo and the residue was dissolved in methanolic sodium methoxide (5 mL of a 25% solution of sodium methoxide in methanol, 21 mmol) and stirred at ambient temperature for 2 h. The reaction was diluted with ethyl acetate, washed with wtaer and brine, dried (MgSO4) and concentrated in vacuo. The residue was purified by flash chromatography (elution with 1:1 hexanes/ethyl acetate) to afford 1.1 g (33%) of the title compound as a solid. LRMS (DCI): 306.3 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06602895B2
Source datasetuspto-grants-2003_08
ORD IDord-fc496f3ce64f4a4983cd54ce74078ae4
Source noteuspto-grants-2003_08