Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 277054Generated: November 3, 2026

Benzyl Bromide → HCID 22629692, compound

https://huagongshe.com/reaction/277054

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantPotassium HydroxideHCID 14797—
ReactantSodium BicarbonateHCID 516892—
Reactant2-Phenyl-7-pyridin-4-yl-[1,2,4]triazolo[1,5-a]pyridin-5-ylamineHCID 22629700—
SolventDimethyl SulfoxideHCID 679—
ProductHCID 22629692HCID 2262969273.3%

Reaction Steps

A solution of 0.20 g (0.0007 mol) 2-phenyl-7-pyridin-4-yl-[1,2,4]triazolo[1,5-a]pyridin-5-ylamine in 17.5 ml dimethylsulfoxide was treated with 0.69 g (0.01 mol) potassiumhydroxide(85%) for 20 minutes at room temperature. Then 0.26 g (0.0015 mol) benzylbromide were added and stirring was continued for 70 hours. Saturated aqueous sodiumbicarbonate was added and the mixture was extracted with chloroform. Evaporation of the solvent and chromatography on silicagel with dichloromethane/methanol 98/2 and crystallisation from diethylether gave 0.12 g (44%) dibenzyl-(2-phenyl-7-pyridin-4-yl-[1,2,4]triazolo[1,5-a]pyridin-5-yl)-amine as light brown crystals. MS m/e (%): 468 (M+H+, 100).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06355653B1
Source datasetuspto-grants-2002_03
ORD IDord-d0eb86f7c4604ec39d5852d9c26501f1
Source noteuspto-grants-2002_03