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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1054956Generated: November 2, 2026

2-(2-(3-(azetidin-1-yl)-1-methyl-1H-1,2,4-triazol-5-yl)vinyl)-5,7-dimethyl-[1,2,4]triazolo[1,5-a]pyrimidine → 2-[2-(5-azetidin-1-yl-2-methyl-2H-[1,2,4]triazol-3-yl)-ethyl]-5,7-dimethyl-[1,2,4]triazolo[1,5-a]pyrimidine

https://huagongshe.com/reaction/1054956

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(2-(3-(azetidin-1-yl)-1-methyl-1H-1,2,4-triazol-5-yl)vinyl)-5,7-dimethyl-[1,2,4]triazolo[1,5-a]pyrimidineHCID 123511508—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product2-[2-(5-azetidin-1-yl-2-methyl-2H-[1,2,4]triazol-3-yl)-ethyl]-5,7-dimethyl-[1,2,4]triazolo[1,5-a]pyrimidineHCID 7270453494.8%

Reaction Conditions

Temperature25 °C

Reaction Steps

A mixture of 2-(2-(3-(azetidin-1-yl)-1-methyl-1H-1,2,4-triazol-5-yl)vinyl)-5,7-dimethyl-[1,2,4]triazolo[1,5-a]pyrimidine (15 mg, 48.3 μmol, Eq: 1.00) and palladium on carbon 10% (5.14 mg, 4.83 μmol, Eq: 0.1) in methanol (15 ml) was stirred for 6 hours at 25° C. under hydrogen atmosphere. The catalyst was filtered off, evaporation of the solvent afforded 2-[2-(5-azetidin-1-yl-2-methyl-2H-[1,2,4]triazol-3-yl)-ethyl]-5,7-dimethyl-[1,2,4]triazolo[1,5-a]pyrimidine (14.3 mg/94.7%) as a light yellow solid. MS: m/z=313.4 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09394311B2
Source datasetuspto-grants-2016_07
ORD IDord-e3e1d5e9a8b94daaa8218e837c796c20
Source noteuspto-grants-2016_07