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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 512597Generated: November 1, 2026

4-Methylmorpholine → 2-(4-(1H-pyrazol-1-yl)phenyl)-N,2-dimethoxy-N-methylacetamide

https://huagongshe.com/reaction/512597

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
ReactantIsobutyl chloroformateHCID 62365—
ReactantMethanamine, N-methoxy-, hydrochloride (1:1)HCID 81138—
Reactantmethyl 2-(4-(1H-pyrazol-1-yl)phenyl)-2-methoxyacetic acidHCID 67388538—
SolventDichloromethaneHCID 6344—
SolventSodium BicarbonateHCID 516892—
Product2-(4-(1H-pyrazol-1-yl)phenyl)-N,2-dimethoxy-N-methylacetamideHCID 5843201676%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of methyl 2-(4-(1H-pyrazol-1-yl)phenyl)-2-methoxyacetic acid (0.18 g, 0.77 mmol) in dry dichloromethane (5 mL) under argon was added N-methylmorpholine (0.18 mL, 1.7 mmol). The reaction mixture was cooled to 0° C., isobutylchloroformate was added, (0.11 mL, 0.85 mmol) and the mixture was stirred for 40 minutes. N,O-dimethylhydroxylamine hydrochloride (0.098 g, 1 mmol) was then added in one portion and slowly allowed to warm to room temperature and stirred for 18 hours. The mixture was diluted with saturated aqueous NaHCO3 and extracted with EtOAc. The combined organics were washed with brine, dried over Na2SO4 and concentrated in vacuo. Purification by chromatography (0-80% EtOAc-hexanes) provided 2-(4-(1H-pyrazol-1-yl)phenyl)-N,2-dimethoxy-N-methylacetamide (0.16 g, 76% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09102643B2
Source datasetuspto-grants-2015_08
ORD IDord-c42c3d84f2224bd5a5e89ac3aa12c6e4
Source noteuspto-grants-2015_08