HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperidin-4-ol → 1-(3-((Phenylsulfonyl)methyl)oxetan-3-yl)piperidin-4-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperidin-4-ol | HCID 79341 | — |
| Reactant | 3-((Phenylsulfonyl)methylene)oxetane | HCID 46203852 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 1-(3-((Phenylsulfonyl)methyl)oxetan-3-yl)piperidin-4-ol | HCID 86708692 | — |
Reaction Steps
A solution of piperidin-4-ol (100 mg, 0.989 mmol) and 3-((phenylsulfonyl)methylene)oxetane (prepared according to a published literature procedure: Wuitschik et al. J. Med. Chem. 53(8) 3227-3246, 2010, 416 mg, 1.977 mmol) in methanol (5 mL) was heated at 50° C. for 20 h. Solvent was evaporated in vacuo and the crude product was purified by flash chromatography on silica gel using an automated ISCO system (40 g column, eluting with 0-8% 2 N ammonia in methanol/dichloromethane). 1-(3-((phenylsulfonyl)methyl)oxetan-3-yl)piperidin-4-ol (300 mg) was obtained as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09273057B2 |
| Source dataset | uspto-grants-2016_03 |
| ORD ID | ord-06abf88058c24f9a9db721fb33e28a78 |
| Source note | uspto-grants-2016_03 |