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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1776257Generated: November 2, 2026

1,8-Diazabicyclo(5.4.0)undec-7-ene → HCID 44537962, compound

https://huagongshe.com/reaction/1776257

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
Reactant4-(Bromoacetyl)pyridine hydrobromideHCID 2776239—
Reactant2-(4-(Quinolin-2-ylmethoxy)phenyl)acetic acidHCID 14500235—
SolventAcetonitrileHCID 6342—
ProductHCID 44537962HCID 4453796215.2%

Reaction Steps

To a solution of 2-(4-(quinolin-2-ylmethoxy)phenyl)acetic acid (3.0 g, 0.01 mol) in acetonitrile (40 mL) were added TEA (1.3 mL, 0.01 mol) and 2-bromo-1-(pyridin-4-yl) ethanone hydrobromide (2.86 g, 0.01 mol) at RT under an inert atmosphere. The reaction mixture was stirred for 1 h followed by addition of DBU (46.6 g, 0.03 mol) at 0° C. and stirring was continued for another 2 h at 0° C. The reaction mixture was quenched with HCl (1 N), aqueous layer was basified with NaHCO3 solution and extracted with DCM (2×50 mL). The combined organic layers were washed with water, dried over Na2SO4 and concentrated in vacuo to obtain the crude product. The crude product was purified via silica gel column chromatography eluting with 25% EtOAc hexanes to afford 4-(pyridin-4-yl)-3-(4-(quinolin-2-ylmethoxy)phenyl)furan-2(5H)-one (600 mg, 15%) as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09265767B2
Source datasetuspto-grants-2016_02
ORD IDord-0400715c00af4b67b4d26fbf814ba136
Source noteuspto-grants-2016_02