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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1692715Generated: November 2, 2026

Ethyl Acetate → HCID 24802657, compound

https://huagongshe.com/reaction/1692715

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
Reactant4-nitro-1H-pyrazol-5-amineHCID 3613991—
ReactantN-[2-chloro-5-(3-dimethylamino-acryloyl)-phenyl]-N-methyl-methanesulfonamideHCID 67279091—
SolventAcetic AcidHCID 176—
ProductHCID 24802657HCID 2480265777%

Reaction Steps

A mixture of 0.050 g (0.39 mmol) of 4-nitro-2H-pyrazol-3-ylamine 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 56 mg of N-{2-chloro-5-[3-nitro-pyrazolo[1,5-a]pyrimidin-7-yl]-phenyl}-N-methyl-methanesulfonamide as a solid (yield 77%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08158632B2
Source datasetuspto-grants-2012_04
ORD IDord-fd12456d62f7493e9bd8adc9e6e4a88c
Source noteuspto-grants-2012_04