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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2174282Generated: October 29, 2026

Ethylene glycol dioxane → 2-(1-(2-fluorobenzyl)-5-(thiazol-2-yl)-1H-1,2,4-triazol-3-yl)isonicotinamide

https://huagongshe.com/reaction/2174282

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylene glycol dioxaneHCID 22419261—
Reactant2-(3-(4-bromopyridin-2-yl)-1-(2-fluorobenzyl)-1H-1,2,4-triazol-5-yl)thiazoleHCID 69094285—
ReactantHCID 178418546HCID 178418546—
SolventSodium chloride; waterHCID 57417360—
Product2-(1-(2-fluorobenzyl)-5-(thiazol-2-yl)-1H-1,2,4-triazol-3-yl)isonicotinamideHCID 6909290411%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a stirring suspension of 2-(3-(4-bromopyridin-2-yl)-1-(2-fluorobenzyl)-1H-1,2,4-triazol-5-yl)thiazole (I-36, 1 equiv) in ethylene glycol-dioxane (approx. 4:1) in a sealed tube was added copper(I) cyanide (3 equiv). The resultant reaction mixture was heated at 100° C. for 24 hr and then cooled to room temperature, treated with brine and extracted with ethyl acetate. The combined organic layers were dried over sodium sulfate, concentrated and purified using SiO2 chromatography (ethyl acetate/hexanes) to afford 2-(1-(2-fluorobenzyl)-5-(thiazol-2-yl)-1H-1,2,4-triazol-3-yl)isonicotinamide as a solid in 11% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09061030B2
Source datasetuspto-grants-2015_06
ORD IDord-462b5e32433448ea8a0ccb44da82d892
Source noteuspto-grants-2015_06