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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1511283Generated: October 26, 2026

1,8-Diazabicyclo(5.4.0)undec-7-ene → 7-Methoxy-4-((5-phenyl-[1,2,3]triazolo[1,5-a]pyridin-3-yl)methoxy)quinoline

https://huagongshe.com/reaction/1511283

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
Reactant4-Acetamidobenzenesulfonyl azideHCID 5129185—
ReactantMethyl 2-(4-phenylpyridin-2-yl)acetateHCID 67503470—
Reactant5-Phenyl-[1,2,3]triazolo[1,5-a]pyridine-3-carboxylateHCID 86630264—
SolventAcetonitrileHCID 6342—
Product7-Methoxy-4-((5-phenyl-[1,2,3]triazolo[1,5-a]pyridin-3-yl)methoxy)quinolineHCID 57691340—

Reaction Steps

5-Phenyl-[1,2,3]triazolo[1,5-a]pyridine-3-carboxylate. To a solution of methyl 2-(4-phenylpyridin-2-yl)acetate (see Lohse, O.; Thevenin, P.; Waldvogel, E. Synlett 1999, 1, 45-48) (0.504 g, 2.22 mmol) in 12 mL CH3CN was added DBU (0.501 ml, 3.33 mmol) and the mixture cooled in an ice bath. To the solution, 4-acetamidobenzenesulfonyl azide (0.533 g, 2.22 mmol) was added and the mixture allowed to warm to rt. The mixture was stirred at rt for 5 h then evaporated. The residue was diluted with CH2Cl2, washed with water, brine, dried over Na2SO4, and filtered. The title compound was obtained after purification via flash chromatography.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08212041B2
Source datasetuspto-grants-2012_07
ORD IDord-d4546e9141e949efa2aab2c4d109494d
Source noteuspto-grants-2012_07