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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 40711Generated: October 29, 2026

Ethyl Acetate → HCID 15604197, compound

https://huagongshe.com/reaction/40711

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
Reactant(5-Amino-1H-pyrazol-4-yl)(thiophen-2-yl)methanoneHCID 11550150—
ReactantHCID 67278716HCID 67278716—
SolventAcetic AcidHCID 176—
ProductHCID 15604197HCID 1560419778.1%

Reaction Steps

A mixture of 0.064 g (0.33 mmol) of (5-amino-1H-pyrazol-4-yl)-thiophene-2-yl-methanone and 0.1 g (0.33 mmol) of N-[5-(3-dimethylamino-acryloyl)-2-fluoro-phenyl]-N-methyl-methanesulfonamide 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 111 mg of N-{2-fluoro-5-[3-(thiophene-2-carbonyl)-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 numberUS08530482B2
Source datasetuspto-grants-2013_09
ORD IDord-2b3da845e47a4ec297eab347c4000f14
Source noteuspto-grants-2013_09