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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1055012Generated: October 31, 2026

(E)-1-(5-(2-(5,8-dimethyl-[1,2,4]triazolo[1,5-a]pyrazin-2-yl)vinyl)-1-methyl-1H-1,2,4-triazol-3-yl)pyrrolidin-2-one → 1-{5-[2-(5,8-dimethyl-[1,2,4]triazolo[1,5-a]pyrazin-2-yl)-ethyl]-1-methyl-1H-[1,2,4]triazol-3-yl}-pyrrolidin-2-one

https://huagongshe.com/reaction/1055012

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(E)-1-(5-(2-(5,8-dimethyl-[1,2,4]triazolo[1,5-a]pyrazin-2-yl)vinyl)-1-methyl-1H-1,2,4-triazol-3-yl)pyrrolidin-2-oneHCID 90026269—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product1-{5-[2-(5,8-dimethyl-[1,2,4]triazolo[1,5-a]pyrazin-2-yl)-ethyl]-1-methyl-1H-[1,2,4]triazol-3-yl}-pyrrolidin-2-oneHCID 7270289699.4%

Reaction Conditions

Temperature25 °C

Reaction Steps

A mixture of (E)-1-(5-(2-(5,8-dimethyl-[1,2,4]triazolo[1,5-a]pyrazin-2-yl)vinyl)-1-methyl-1H-1,2,4-triazol-3-yl)pyrrolidin-2-one (24 mg, 70.9 μmol, Eq: 1.00) and palladium on carbon 10% (7.5 mg, 7.1 μmol, Eq: 0.1) in methanol (15 ml) was stirred for 5 hours at 25° C. under hydrogen atmosphere. Additional catalyst (0.1 eq) was added and hydrogenation continued for another 6 hours until HPLC shows complete conversion. The catalyst was filtered off, the filtrate was evaporated affording 1-{5-[2-(5,8-dimethyl-[1,2,4]triazolo[1,5-a]pyrazin-2-yl)-ethyl]-1-methyl-1H-[1,2,4]triazol-3-yl}-pyrrolidin-2-one (24 mg, 99.4%) as a colorless oil. MS: m/z=341.6 (M+H+)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09394311B2
Source datasetuspto-grants-2016_07
ORD IDord-b14ae0a748634a27882ce413bdbd8bb9
Source noteuspto-grants-2016_07