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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Reactant | 4-(Bromoacetyl)pyridine hydrobromide | HCID 2776239 | — |
| Reactant | 2-(4-(Quinolin-2-ylmethoxy)phenyl)acetic acid | HCID 14500235 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 44537962 | HCID 44537962 | 15.2% |
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 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08481534B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-3a348bf143824e5a9869f7b92111d3ec |
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| Source note | uspto-grants-2013_07 |
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