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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1045728Generated: November 1, 2026

Tetrahydrofuran → HCID 58447041, compound

https://huagongshe.com/reaction/1045728

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
Reactant6-Bromo-8-chloro[1,2,4]triazolo[4,3-a]pyrazineHCID 58446985—
SolventWaterHCID 962—
ProductHCID 58447041HCID 5844704189.4%

Reaction Steps

A 100 mL round bottom flask was charged with 6-bromo-8-chloro-[1,2,4]triazolo[4,3-a]pyrazine (1.11 g, 4.73 mmol), tert-butyl piperazine-1-carboxylate (2.64 g, 14.2 mmol) and THF (50 mL). The resulting mixture was stirred at room temperature for 0.5 h. Reaction progress was monitored by TLC (EtOAc/petroleum ether=1:2). Work-up: the reaction mixture was diluted with water and extracted with EtOAc (50 mL×3). The combined organic layers were dried over anhydrous Na2SO4 and concentrated in vacuo. The residue was further purified by flash column chromatography on silica gel with 20% EtOAc in petroleum ether, to afford 1.62 g (89%) of the product as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08569300B2
Source datasetuspto-grants-2013_10
ORD IDord-cdb600c200644bc5ac4f4a30f414abf5
Source noteuspto-grants-2013_10