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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 930349Generated: October 29, 2026

1,8-Diazabicyclo(5.4.0)undec-7-ene → HCID 86732169, compound

https://huagongshe.com/reaction/930349

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 86732168HCID 86732168—
SolventMethanolHCID 887—
ProductHCID 86732169HCID 86732169—

Reaction Conditions

Temperature75 °C

Reaction Steps

To a 20 mL resealable vial was added N-((4S,6S)-4-(6-bromo-3-fluoropyridin-2-yl)-4-(fluoromethyl)-6-(trifluoromethyl)-5,6-dihydro-4H-1,3-oxazin-2-yl)benzamide (0.500 g, 1.046 mmol), MeOH (10 mL) and finally 1,8-diazabicyclo-[5.4.0]undec-7-ene (Aldrich; 0.312 mL, 2.091 mmol). The vial was sealed and stirred at 75° C. for 2 h. The reaction mixture was poured into sat NaHCO3 and extracted with EtOAc. The combined extracts were washed with water and then dried (Na2SO4) and concentrated onto silica. Purification by silica gel chromatography (Gradient: 0.0 to 9.0% MeOH/CH2Cl2) afforded (4S,6S)-4-(6-bromo-3-fluoropyridin-2-yl)-4-(fluoromethyl)-6-(trifluoromethyl)-5,6-dihydro-4H-1,3-oxazin-2-amine. The material still contained some impurities. MS m/z=375.8 [M+H]+. Calculated for C11H9BrF5N3O: 375.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09296734B2
Source datasetuspto-grants-2016_03
ORD IDord-a0f49dbd7276497194ad519eb07f69e4
Source noteuspto-grants-2016_03