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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1672482Generated: October 31, 2026

1,8-Diazabicyclo(5.4.0)undec-7-ene → HCID 178489836, compound

https://huagongshe.com/reaction/1672482

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
Reactant2-Chloro-8-methoxy-7-methylquinazolineHCID 46941845—
ReactantHCID 178511715HCID 178511715—
SolventAcetonitrileHCID 6342—
ProductHCID 178489836HCID 17848983660.5%

Reaction Steps

To a solution of 2-chloro-8-methoxy-7-methylquinazoline (20.4 g, 0.098 mol) in CH3CN (800 mL) were added trans-4-amino-cyclohexanol (22.5 g, 0.195 mol) and DBU (29.7 g, 0.195 mol) in one portion. The reaction mixture was refluxed with stirring overnight. TLC (ethyl acetate/petroleum ether=1:1) indicated the reaction was complete. The solvent was removed in vacuo. The residue was taken up with CHCl3 (550 mL), the solution was washed with water (150 mL×2). The aqueous layer was re-extracted with CHCl3 (150 mL). The combined organic layers were washed with brine, dried over anhydrous Na2SO4 and concentrated in vacuo to give the crude product. The crude product was re-crystallized from EtOH (130 mL)/water (200 mL) to give the title compound (17 g, 60.5%) as an off-white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07998978B2
Source datasetuspto-grants-2011_08
ORD IDord-71786d32a09b40df9d265d888f143ba1
Source noteuspto-grants-2011_08