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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1411973Generated: November 1, 2026

tert-Butyl [1,2,4]triazolo[1,5-a]pyrazin-2-ylcarbamate → tert-Butyl (5,6,7,8-tetrahydro-[1,2,4]triazolo[1,5-a]pyrazin-2-yl)carbamate

https://huagongshe.com/reaction/1411973

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl [1,2,4]triazolo[1,5-a]pyrazin-2-ylcarbamateHCID 89548973—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Producttert-Butyl (5,6,7,8-tetrahydro-[1,2,4]triazolo[1,5-a]pyrazin-2-yl)carbamateHCID 8668451168.8%

Reaction Conditions

Temperature60 °C

Reaction Steps

A 100-mL round-bottomed flask was purged with nitrogen and charged with 270c (1.0 g, 4.25 mmol), 20% palladium on carbon (10% wet, 200 mg), and ethanol (40 mL). It was then evacuated, charged with hydrogen gas (25 atm), and stirred at 60° C. for 24 h. The hydrogen was evacuated and nitrogen was charged into the flask. The catalyst was removed by filtration through a pad of CELITE® and the filtrate was concentrated under reduced pressure to afford 270d (700 mg, 68%). MS-ESI: [M-t-Bu]+ 184.0

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08921353B2
Source datasetuspto-grants-2014_12
ORD IDord-d9fb9308718a4d12a99ce1957688b88c
Source noteuspto-grants-2014_12