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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 890181Generated: October 30, 2026

N,N-Dimethylaniline → Ethyl 4-(7-(butyl)-3-mesityl-2,5-dimethylpyrazolo[1,5-a]pyrimidin-6-yl)butanoate

https://huagongshe.com/reaction/890181

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N-DimethylanilineHCID 949—
ReactantButylamineHCID 8007—
ReactantPotassium CarbonateHCID 11430—
ReactantChlorine monoxideHCID 24646—
ReactantHCID 178471269HCID 178471269—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
ProductEthyl 4-(7-(butyl)-3-mesityl-2,5-dimethylpyrazolo[1,5-a]pyrimidin-6-yl)butanoateHCID 22249666—

Reaction Steps

Phosphoeus oxychloride (11.3 g) and N,N-dimethylaniline (3 droplets) were added to ethyl 4-(3-mesityl-2,5-dimethyl-7-oxo-4,7-dihydropyrazolo[1,5-a]pyrimidin-6-yl)butanoate (700 mg, 1.77 mmol), followed by heating under reflux for 1.5 hours. After the reaction, it was treated with ice-water, neutralized with potassium carbonate, extracted with ethyl acetate, dried over anhydrous magnesium sulfate and evaporated. The resulting reaction residue was dissolved in acetonitrile (5 ml) and n-butylamine (2 mL) was added, followed by heating under reflux for six hours. After the reaction, it was treated with water, and then neutralized with potassium carbonate, extracted with ethyl acetate, dried over anhydrous magnesium sulfate and evaporated. The residue was purified by silica gel column chromatography (10-25% ethyl acetate/hexane), to give the title compound (2.5 g) as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06995163B2
Source datasetuspto-grants-2006_02
ORD IDord-7da826292c13472db7a44b69eb27b86a
Source noteuspto-grants-2006_02