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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 231518Generated: October 27, 2026

Pyrazolo(1,5-a)pyrimidine-3-carbonitrile → 4,5,6,7-Tetrahydropyrazolo[1,5-a]pyrimidine-3-carbonitrile

https://huagongshe.com/reaction/231518

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyrazolo(1,5-a)pyrimidine-3-carbonitrileHCID 819275—
ReactantSodium borohydrideHCID 4311764—
SolventMethanolHCID 887—
Product4,5,6,7-Tetrahydropyrazolo[1,5-a]pyrimidine-3-carbonitrileHCID 13567137242.6%

Reaction Steps

To a stirred mixture of 4.0 g of pyrazolo[1,5-a]-pyrimidine-3-carbonitrile in 200 ml of methyl alcohol under nitrogen at, room temperature, was added, one at a time, 3 pellets of sodium borohydride. The mixture was stirred for several hours and then was allowed to stand at room temperature. The product was collected by filtration to give 1.75 g of 4,5,6,7-tetrahydropyrazolo[1,5-a]pyrimidine-3-carbonitrile, mp 206°-207° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04847256
Source datasetuspto-grants-1989_07
ORD IDord-5ca1c1690f7d49e9a1dc6efbd26ea0b6
Source noteuspto-grants-1989_07