HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1384279Generated: November 2, 2026
1,8-Diazabicyclo(5.4.0)undec-7-ene → HCID 21186685, compound
https://huagongshe.com/reaction/1384279
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Reactant | HCID 21186666 | HCID 21186666 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 21186685 | HCID 21186685 | 97.5% |
Reaction Steps
In an atmosphere of argon, ethyl 9-chloro-2-methyl-6,7,8,9-tetrahydro-5H-cyclohepta[b]pyridine-3-carboxylate (3.35 g, 12.5 mmol) was dissolved in toluene (12.0 ml), and the solution was mixed with 1,8-diazabicyclo[5.4.0]-7-undecene (DBU) (2.9 ml, 18.9 mmol) at 0° C. and then heated under reflux for 23 hours. The solvent was evaporated under reduced pressure, and the thus obtained residue was dissolved in ethyl acetate, mixed with water and then extracted with ethyl acetate. The thus obtained organic layer was washed with water and saturated brine in that order and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure and the resulting residue was purified by a silica gel column chromatography (ether:hexane=1:2) to obtain the title compound (2.82 g, 97.5%) as pale yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06258829B1 |
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| Source dataset | uspto-grants-2001_07 |
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| ORD ID | ord-3f74638ead204489a023eb9bf2433257 |
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| Source note | uspto-grants-2001_07 |
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