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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 446799Generated: October 29, 2026

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

https://huagongshe.com/reaction/446799

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 Conditions

Temperature0 °C

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 and then cooled to 0° C. DBU (46.6 g, 0.03 mol) was then added and the reaction mixture was stirred for 2 h at 0° C. and quenched with HCl (1 N). The aqueous layer was basified with a 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 material was purified via silica gel column chromatography eluting with 25% EtOAc in 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 numberUS08481534B2
Source datasetuspto-grants-2013_07
ORD IDord-3a348bf143824e5a9869f7b92111d3ec
Source noteuspto-grants-2013_07