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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 394807Generated: October 29, 2026

Methyl bromoacetate → 1-[(4-Methoxy)phenyl]-3-[(methoxycarbonyl)methylamino]-1H-pyrazole

https://huagongshe.com/reaction/394807

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl bromoacetateHCID 60984—
ReactantSodium BicarbonateHCID 516892—
Reactant1-[(4-Methoxy)phenyl]-3-[(methoxycarbonyl)amino]-1H-pyrazoleHCID 54344399—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product1-[(4-Methoxy)phenyl]-3-[(methoxycarbonyl)methylamino]-1H-pyrazoleHCID 8658798089.7%

Reaction Conditions

Temperature85 °C

Reaction Steps

To a solution of 1-[(4-methoxy)phenyl]-3-amino-1H-pyrazole-5-[(2′-tert-butylaminosulfonyl-[1,1′]-biphen-4-yl)carboxyamide (1.0 g, 1.92 mmol) in 10 mL of DMF was added sodium bicarbonate (0.24 g, 2.88 mmol) and methyl bromoacetate (0.22 mL, 2.30 mmol) The resulting mixture was stirred at 85° C. for 16 h. The reaction was not complete so additional portions of sodium bicarbonate (0.48 g, 5.76 mmol) and methyl bromoacetate (0.22 mL, 2.30 mmol) were added and the reaction was stirred at 95° C. for 6 h longer. The reaction was cooled to ambient temperature and was diluted with ethyl acetate. The organics were washed with brine, dried (MgSO4) and concentrated in vacuo. The residue was dissolved in 5 mL of trifluoroacetic acid and was stirred at reflux for 20 min and then was cooled to ambient temperature and concentrated in vacuo. The residue was purified by prep HPLC (C18 reverse phase column, elution with a H2O/CH3CN gradient with 0.5% TFA) and lyophilized to afford 450 mg (44%) of the title compound as a white powder. LRMS (ES+): 536.0 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06602895B2
Source datasetuspto-grants-2003_08
ORD IDord-035d58402bef4869b209a771736a4283
Source noteuspto-grants-2003_08