Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 231528Generated: October 31, 2026

Sodium cyanoborohydride → HCID 135671363, compound

https://huagongshe.com/reaction/231528

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant7-[3-(Trifluoromethyl)phenyl]pyrazolo[1,5-a]pyrimidineHCID 19756203—
SolventAcetic AcidHCID 176—
SolventChloroformHCID 6212—
ProductHCID 135671363HCID 13567136324.6%

Reaction Steps

To a stirred mixture of 25.0 g of 7-[3-(trifluoromethyl)phenyl]pyrazolo[1,5-a]pyrimidine in 250 ml of glacial acetic acid, at room temperature, under nitrogen was added portionwise 14.92 g of sodium cyanoborohydride. The resultant solution was stirred for 24 hours, and then was evaporated in vacuo to give an oil. The oil was dissolved in chloroform and washed with saturated sodium bicarbonate. The organic layer was separated, dried over anhydrous sodium sulfate and filtered. The filtrate was evaporated in vacuo to give a semi-solid which was chromatographed on a silica gel column using a mixture of 25% ethyl acetate and 75% hexane as the solvent system. The product fraction was collected and evaporated to give 6.2 g of the desired product as orange crystals, mp 61°-64° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04847256
Source datasetuspto-grants-1989_07
ORD IDord-ffcc17ed6f1145efb091c0b8192fa51c
Source noteuspto-grants-1989_07