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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2242885Generated: October 31, 2026

Phenol → 2-Furan-2-yl-6-(3-phenoxy-prop-1-ynyl)-[1,2,4]triazolo[1,5-a]pyrazin-8-ylamine

https://huagongshe.com/reaction/2242885

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenolHCID 996—
ReactantPropargyl alcoholHCID 7859—
ReactantTriphenylphosphineHCID 11776—
ReactantDiisopropyl diazene-1,2-dicarboxylateHCID 75555—
Reactant[1,2,4]Triazolo[1,5-a]pyrazin-8-amine, 6-bromo-2-(2-furanyl)-HCID 71401630—
Product2-Furan-2-yl-6-(3-phenoxy-prop-1-ynyl)-[1,2,4]triazolo[1,5-a]pyrazin-8-ylamineHCID 11232803—

Reaction Steps

Alternatively, a compound of formula (I) can react with an alkynyl (e.g., a compound of the formula L′-X1a where L′ is a precursor of L and X1a has been defined above) to form an intermediate, which can further react with a compound of the formula R1—X3—Y—X2-L″ to form a compound of formula (I). As an example, 6-bromo-2-furan-2-yl-[1,2,4]triazolo[1,5-a]pyrazin-8-ylamine can react with prop-2-yn-1-ol to form 3-(8-amino-2-furan-2-yl-[1,2,4]triazolo[1,5-a]pyrazin-6-yl)-prop-2-1-ol, which can then react with phenol in the presence of triphenyl phosphine and diisopropyl azodicarboxylate to form 2-furan-2-yl-6-(3-phenoxy-prop-1-ynyl)-[1,2,4]triazolo[1,5-a]pyrazin-8-ylamine, a compound of formula (I). See, e.g., Example 22 below.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07674791B2
Source datasetuspto-grants-2010_03
ORD IDord-cd222f27e4ed46a599702c3459c014d7
Source noteuspto-grants-2010_03