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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 610146Generated: October 30, 2026

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

https://huagongshe.com/reaction/610146

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 water 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 numberUS05998424
Source datasetuspto-grants-1999_12
ORD IDord-9b8cc2768d154fd8bf99320a0514aabd
Source noteuspto-grants-1999_12