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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1692720Generated: November 2, 2026

Ethyl Acetate → HCID 24802662, compound

https://huagongshe.com/reaction/1692720

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantN-[2-chloro-5-(3-dimethylamino-acryloyl)-phenyl]-N-methyl-methanesulfonamideHCID 67279091—
ReactantHCID 178434678HCID 178434678—
SolventAcetic AcidHCID 176—
ProductHCID 24802662HCID 2480266260.7%

Reaction Steps

A mixture of 0.048 g (0.39 mmol) of 5-amino-3-methyl-1H-pyrazole-4-carbonitrile and 0.124 g (0.39 mmol) of N-[5-(3-dimethylamino-acryloyl)-2-chloro-phenyl]-N-methyl-methanesulfonamide in 12 mL of glacial acetic acid was refluxed for 1.5 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 89 mg of N-{2-chloro-5-[3-cyano-2-methyl-pyrazolo[1,5-a]pyrimidin-7-yl]-phenyl}-N-methyl-methanesulfonamide as a solid (yield 60.5%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08158632B2
Source datasetuspto-grants-2012_04
ORD IDord-a316cbe3e02c4afd9c6239dff88a8033
Source noteuspto-grants-2012_04