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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantHCID 21186666HCID 21186666—
SolventTolueneHCID 1140—
ProductHCID 21186685HCID 2118668597.5%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06258829B1
Source datasetuspto-grants-2001_07
ORD IDord-3f74638ead204489a023eb9bf2433257
Source noteuspto-grants-2001_07