HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phthalimide → (1S,2S,5R)-2-(3-benzyl-7,7-difluoro-3-azabicyclo[3.3.0]oct-2-ylmethyl)-isoindole-1,3-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phthalimide | HCID 6809 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Diethyl azodicarboxylate | HCID 5462977 | — |
| Reactant | (3-Benzyl-7,7-difluoro-3-azabicyclo[3.3.0]oct-2-yl)-methanol | HCID 66703990 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | Ethylacetate heptane | HCID 21899848 | — |
| Product | (1S,2S,5R)-2-(3-benzyl-7,7-difluoro-3-azabicyclo[3.3.0]oct-2-ylmethyl)-isoindole-1,3-dione | HCID 59411625 | 64% |
Reaction Steps
To a cold solution of triphenylphosphine (1.8 g) in dry THF (90 mL) was added dropwise DEAD 40% in toluene (3.15 mL). Then was added successively phthalimide (1.01 g) and a solution of (3-benzyl-7,7-difluoro-3-azabicyclo[3.3.0]oct-2-yl)-methanol (WO03/062265) (1.83 g) in dry THF (10 mL). The reaction mixture was stirred at RT overnight, diluted with EA, washed with water. The organic phase was washed with sat. NaHCO3 solution, dried (MgSO4), filtered and concentrated to yield a crude oil. FC (n-heptane/EA: 7/3 to 1/1) gave 1.73 g (64%) of the title compound as a white solid. LC-MS: tR=0.87 min; [M+H]+=397.47.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08106215B2 |
| Source dataset | uspto-grants-2012_01 |
| ORD ID | ord-3d60d04688e7468f9739125c9dabb199 |
| Source note | uspto-grants-2012_01 |