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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 40714Generated: October 29, 2026

Ethyl Acetate → HCID 15604199, compound

https://huagongshe.com/reaction/40714

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
Reactant(5-Amino-1H-pyrazol-4-yl)(thiophen-2-yl)methanoneHCID 11550150—
ReactantN-[5-(3-dimethylamino-acryloyl)-2-fluoro-phenyl]-N-prop-2-ynyl-methanesulfonamideHCID 73199327—
SolventAcetic AcidHCID 176—
ProductHCID 15604199HCID 1560419961.3%

Reaction Steps

A mixture of 0.108 g (0.56 mmol) of (5-amino-1H-pyrazol-4-yl)-thiophene-2-yl-methanone and 0.198 g (0.61 mmol) of N-[5-(3-dimethylamino-acryloyl)-2-fluoro-phenyl]-N-prop-2-ynyl-methanesulfonamide in 10 ml of glacial acetic acid was refluxed for 2 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 156 mg of N-{2-fluoro-5-[3-(thiophene-2-carbonyl)-pyrazolo[1,5-a]pyrimidin-7-yl]-phenyl}-N-prop-2-ynyl-methanesulfonamide as a solid (yield 61%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08530482B2
Source datasetuspto-grants-2013_09
ORD IDord-4ce98f8e329b4c67a028c73f81045ca5
Source noteuspto-grants-2013_09