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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 893649Generated: October 25, 2026

Acetamide → N-[3-(3-cyano-4,5-dihydropyrazolo[1,5-a]pyrimidin-7-yl)phenyl]acetamide

https://huagongshe.com/reaction/893649

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetamideHCID 178—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantN-[3-(3-Dimethylaminoacryloyl)phenyl]acetamideHCID 53412415—
ReactantHCID 178510443HCID 178510443—
SolventAcetic AcidHCID 176—
ProductN-[3-(3-cyano-4,5-dihydropyrazolo[1,5-a]pyrimidin-7-yl)phenyl]acetamideHCID 136093204—

Reaction Steps

A mixture of 7.0 g of 3'-actamido-3-(N,N-dimethylamino)acrylophenone and 3.3 g. of 3-amino-4-cyanopyrazole in 100 ml of acetic acid was heated at reflux for 8 hours. Crystals that formed on cooling were filtered and dried to give 7.4 g. of N-[3-(3-cyano-pyrazolo[1,5-a]pyrimidin-7-yl)phenyl[acetamide, m.p. 254°-256° C. This was reacted with 14.8 g of sodium cyanoborohydride in 50 ml of acetic acid to give 3.0 g of N-[3-(3-cyano-4,5-dihydropyrazolo[1,5-a]pyrimidin-7-yl)phenyl]acetamide, m.p. 251°-254° C. This is reacted with chloroacetic anhydride and sodium carbonate in toluene as in Example 3 to give the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05126340
Source datasetuspto-grants-1992_06
ORD IDord-d6be92ae7e474258ba1710bf6b89e926
Source noteuspto-grants-1992_06