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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1692713Generated: October 30, 2026

Ethyl Acetate → HCID 24805142, compound

https://huagongshe.com/reaction/1692713

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
Reactant5-Amino-4-cyanopyrazoleHCID 85515—
ReactantN-[2-chloro-5-(3-dimethylamino-acryloyl)-phenyl]-N-methyl-acetamideHCID 67279027—
SolventAcetic AcidHCID 176—
ProductHCID 24805142HCID 2480514277.1%

Reaction Steps

A mixture of 0.046 g (0.43 mmol) of 5-amino-1H-pyrazole-4-carbonitrile and 0.120 g (0.43 mmol) of N-[5-(3-dimethylamino-acryloyl)-2-chloro-phenyl]-N-methyl-acetamide in 10 mL of glacial acetic acid was refluxed for 2.5 hours and then the solvent was removed by reduced pressure distillation. To the resulting residue were added 15 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 108 mg of N-{2-chloro-5-[3-cyano-pyrazolo[1,5-a]pyrimidin-7-yl]-phenyl}-N-methyl-acetamide as a solid (yield 77%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08158632B2
Source datasetuspto-grants-2012_04
ORD IDord-60d86286c5db4d7fae67b3ff9bf4c638
Source noteuspto-grants-2012_04