HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diazabicyclo[5.4.0]undec-7-ene → HCID 11253149, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diazabicyclo[5.4.0]undec-7-ene | HCID 9834010 | — |
| Reactant | HCID 58911259 | HCID 58911259 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 11253149 | HCID 11253149 | 80% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07763644B2 |
| Source dataset | uspto-grants-2010_07 |
| ORD ID | ord-39de803e9a4f4ac9a9f45eced3e2ad43 |
| Source note | uspto-grants-2010_07 |