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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 876475Generated: October 29, 2026

Tetrahydrofuran → Tert-butyl 4-(2-([1,2,4]triazolo[4,3-a]pyridin-3-yl)-6-fluoroquinolin-8-yloxy)-3,3-difluoropiperidine-1-carboxylate

https://huagongshe.com/reaction/876475

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantPotassium tert-butoxideHCID 23665647—
Reactanttert-Butyl 3,3-difluoro-4-hydroxypiperidine-1-carboxylateHCID 56932106—
Reactant2-([1,2,4]Triazolo[4,3-a]pyridin-3-yl)-6,8-difluoroquinolineHCID 67230475—
SolventDimethylformamideHCID 6228—
ProductTert-butyl 4-(2-([1,2,4]triazolo[4,3-a]pyridin-3-yl)-6-fluoroquinolin-8-yloxy)-3,3-difluoropiperidine-1-carboxylateHCID 67234219—

Reaction Steps

tert-Butyl 3,3-difluoro-4-hydroxypiperidine-1-carboxylate (0.0706 g, 0.298 mmol) was treated with 1 M KOtBu in THF (0.283 mL, 0.283 mmol) and stirred for 15 minutes. The solution was treated with 2-([1,2,4]triazolo[4,3-a]pyridin-3-yl)-6,8-difluoroquinoline (0.042 g, 0.149 mmol) and DMF (0.80 mL) then the mixture was stirred at ambient temperature for 16 hours. The mixture was directly chromatographed on SiO2 eluting with a gradient of 2% NH4OH in isopropanol/ethyl acetate. The desired product was collected and concentrated to a colorless oil, (72 mg). MS APCI (+) m/z 500.0 (M+1) detected.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08987251B2
Source datasetuspto-grants-2015_03
ORD IDord-2535f08836c74f35ba1f10b05f99e767
Source noteuspto-grants-2015_03