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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1295806Generated: November 2, 2026

Diazabicyclo[5.4.0]undec-7-ene → HCID 11253149, compound

https://huagongshe.com/reaction/1295806

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiazabicyclo[5.4.0]undec-7-eneHCID 9834010—
ReactantHCID 58911259HCID 58911259—
SolventChloroformHCID 6212—
ProductHCID 11253149HCID 1125314980%

Reaction Steps

In a 50 ml three necked flask fitted with a magnetic stirrer, under inert atmosphere, 4-(2-bromo-2,2-difluoro-ethyl)-1-(1H-imidazol-1-ylmethyl)-pyrrolidin-2-one 17 (0.16 g, 0.52 mmol) and diazabicyclo [5.4.0]undec-7-ene (0.1 ml, 0.62 mmol) in CHCl3 (0.5 ml) are stirred overnight at room temperature. The reaction mixture is filtered, evaporated in vacuo, diluted with CH2Cl2 and the organic layer is washed with water, dried over MgSO4, filtered and evaporated in vacuo. The residue is purified by chromatography on silicagel (CH2Cl2/EtOH/NH4OH: 93.5/06/0.5 (v/v/v)) to afford 4-(2,2-difluorovinyl)-1-(1H-imidazol-1-ylmethyl)pyrrolidin-2-one 18 (0.092 g, 80%) which is crystallized as a maleic salt in THF.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07244747B2
Source datasetuspto-grants-2007_07
ORD IDord-42e8253497cf4bc7865da156faf57303
Source noteuspto-grants-2007_07