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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 522880Generated: October 27, 2026

3-(4-Chlorophenyl)-[1,2,4]triazolo[4,3-a]pyrazine → 3-(4-chlorophenyl)-5H,6H,7H,8H-[1,2,4]triazolo[4,3-a]pyrazine

https://huagongshe.com/reaction/522880

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(4-Chlorophenyl)-[1,2,4]triazolo[4,3-a]pyrazineHCID 67376781—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product3-(4-chlorophenyl)-5H,6H,7H,8H-[1,2,4]triazolo[4,3-a]pyrazineHCID 6258572386%

Reaction Steps

3-(4-Chlorophenyl)-[1,2,4]triazolo[4,3-a]pyrazine (2.01 g) was hydrogenated under atmospheric hydrogen with 10% Pd/C (400 mg Celite® (diatomaceous earth)) as a catalyst in ethanol (20 mL) at RT for 18 h. The reaction mixture was filtered through and concentrated. Purification by flash chromatography (silica gel, 10% methanol/dichloromethane) afforded 3-(4-chlorophenyl)-5,6,7,8-tetrahydro-[1,2,4]triazolo[4,3-a]pyrazine (86% yield) as a viscous oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09334269B2
Source datasetuspto-grants-2016_05
ORD IDord-6db126ed972945b49dedaf0f059a6525
Source noteuspto-grants-2016_05