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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1526540Generated: November 2, 2026

1,8-Diazabicyclo(5.4.0)undec-7-ene → HCID 90389292, compound

https://huagongshe.com/reaction/1526540

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantHCID 90389345HCID 90389345—
SolventMethanolHCID 887—
ProductHCID 90389292HCID 9038929265.1%

Reaction Conditions

Temperature40 °C

Reaction Steps

N-(5-(difluoromethyl)-5-(3-fluoro-2-methylphenyl)-2-oxa-4-azabicyclo[4.1.0]hept-3-en-3-yl)benzamide (1.0 g, 2.67 mmol) was dissolved in methanol (50 mL) under nitrogen and 1,8-diazabicyclo-[5.4.0]undec-7-ene (0.798 ml, 5.34 mmol) was added. The reaction was heated to 40° C. After 18 hours, the reaction mixture was concentrated to dryness under reduced pressure and the residue partitioned between water and ethyl acetate. The organic layer was isolated and concentrated under reduced pressure. The crude residue was purified via silica gel flash chromatography eluting with 0-60% ethyl acetate in hexanes afforded the title compound 5-(difluoromethyl)-5-(3-fluoro-2-methylphenyl)-2-oxa-4-azabicyclo[4.1.0]hept-3-en-3-amine (0.470 g, 1.739 mmol, 65.1% yield). LC/MS (ESI+) m/z=270.9 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09085576B2
Source datasetuspto-grants-2015_07
ORD IDord-e1393094838c4e08a93c2dac25e5f685
Source noteuspto-grants-2015_07