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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 56498Generated: October 30, 2026

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

https://huagongshe.com/reaction/56498

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 numberUS09434707B2
Source datasetuspto-grants-2016_09
ORD IDord-270dd1c6e4a848f3a88a3b0c86518f21
Source noteuspto-grants-2016_09