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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Reactant | 2-Chloro-8-methoxy-7-methylquinazoline | HCID 46941845 | — |
| Reactant | HCID 178511715 | HCID 178511715 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 178489836 | HCID 178489836 | 60.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07998978B2 |
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| Source dataset | uspto-grants-2011_08 |
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| ORD ID | ord-71786d32a09b40df9d265d888f143ba1 |
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| Source note | uspto-grants-2011_08 |
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