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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 550561Generated: October 25, 2026

Ethyl Acetate → N-[3-(3-cyano-pyrazolo[1,5-a]pyrimidin-7-yl)-phenyl]-N-ethyl-methanesulfonamide

https://huagongshe.com/reaction/550561

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
Reactant5-Amino-4-cyanopyrazoleHCID 85515—
ReactantN-[3-[3-(dimethylamino)-1-oxo-2-propenyl]phenyl)-N-ethyl-methanesulfonamideHCID 67198287—
SolventAcetic AcidHCID 176—
ProductN-[3-(3-cyano-pyrazolo[1,5-a]pyrimidin-7-yl)-phenyl]-N-ethyl-methanesulfonamideHCID 1165303652.4%

Reaction Steps

A mixture of 0.196 g (1.82 mmol) of 4-cyano-2H-pyrazol-3-ylamine and 0.54 g (1.82 mmol) of N-[3-[3-(dimethylamino)-1-oxo-2-propenyl]phenyl]-N-ethyl-methanesulfonamide in 10 ml of glacial acetic acid was refluxed for 8 hours and then the solvent was removed by reduced pressure distillation. To the resulting residue were added 10 ml of dichloromethane and 10 ml of saturated sodium bicarbonate solution. The two layers were separated, and the aqueous layer was washed with 10 ml of dichloromethane. The organic layers were washed with 10 ml of water and dried over magnesium sulfate. The dichloromethane layer was evaporated to dryness to yield an oil which, in the presence of ethyl acetate, gave 324 mg of N-[3-(3-cyano-pyrazolo[1,5-a]pyrimidin-7-yl)-phenyl]-N-ethyl-methanesulfonamide as a yellow solid (yield 52.4%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07947688B2
Source datasetuspto-grants-2011_05
ORD IDord-e032f0561f5749b7b00f522d40231695
Source noteuspto-grants-2011_05