HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetone → 2-{6-[4-(4-Benzyl-phthalazin-1-yl)-piperazin-1-yl]-pyridin-3-yl}-propane-1,2-diol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Sulfite | HCID 24437 | — |
| Reactant | Methyl morpholine oxide | HCID 82029 | — |
| Reactant | HCID 44186377 | HCID 44186377 | — |
| Catalyst | Potassium osmate(VI) dihydrate | HCID 53393272 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Product | 2-{6-[4-(4-Benzyl-phthalazin-1-yl)-piperazin-1-yl]-pyridin-3-yl}-propane-1,2-diol | HCID 44186378 | 72% |
Reaction Steps
To 1-benzyl-4-[4-(5-isopropenyl-pyridin-2-yl)-piperazin-1-yl]-phthalazine (68 mg, 0.158 mmol) is added acetone (1 mL), t-butanol (0.5 mL), and H2O (0.5 mL). To this suspension is then added potassium osmate (VI) dihydrate (536 μg, 1.58 μM), and NMO (21 mg, 0.174 mmol), and the reaction is stirred at room temperature for 3 h. Sodium sulfite (350 mg) is added to the resulting clear orange solution and the mixture is stirred for 1 h. Additional H2O (25 mL) is added, and the organics extracted with EtOAc (3×25 mL), dried over MgSO4, and concentrated. Purification by flash chromatography on silica gel (90:10 CH2Cl2:MeOH) afforded a clear oil which was then triturated with EtOAc to afford the title compound as a white powder (52 mg, 72% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08536168B2 |
| Source dataset | uspto-grants-2013_09 |
| ORD ID | ord-009f8c573ce6455c8b254aa7822ef177 |
| Source note | uspto-grants-2013_09 |