Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 40713Generated: October 30, 2026

Ethyl Acetate → HCID 15604198, compound

https://huagongshe.com/reaction/40713

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
Reactant(5-Amino-1H-pyrazol-4-yl)(thiophen-2-yl)methanoneHCID 11550150—
ReactantN-[2-chloro-5-(3-dimethylamino-acryloyl)-phenyl]-N-methyl-methanesulfonamideHCID 67279091—
SolventAcetic AcidHCID 176—
ProductHCID 15604198HCID 1560419873%

Reaction Steps

A mixture of 0.076 g (0.39 mmol) of (5-amino-1H-pyrazol-4-yl)-thiophene-2-yl-methanone and 0.124 g (0.39 mmol) of (N-[2-chloro-5-(3-dimethylamino-acryloyl)-phenyl]-N-methyl-methanesulfonamide in 10 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 128 mg of N-{2-chloro-5-[3-(thiophene-2-carbonyl)-pyrazolo[1,5-a]pyrimidin-7-yl]-phenyl}-N-methyl-methanesulfonamide as a solid (yield 73%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08530482B2
Source datasetuspto-grants-2013_09
ORD IDord-dbbb60323e7244509be036ad9dd5071a
Source noteuspto-grants-2013_09