HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperidine → 4-{2-(4-piperidin-1-ylmethyl-piperidin-1-yl)-benzyl}-morpholine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | HCID 58978046 | HCID 58978046 | — |
| Solvent | 1,1-Dichloroethane | HCID 6365 | — |
| Product | 4-{2-(4-piperidin-1-ylmethyl-piperidin-1-yl)-benzyl}-morpholine | HCID 10043902 | — |
Reaction Steps
A solution of the product of Example 17 (288 mg) and piperidine (0.12 mL) in dichloroethane (DCE, 2 mL) was treated with sodium triacetoxyborohydride (297 mg). After 16 h, the resulting mixture was treated with 10% potassium hydroxide (2 mL), and extracted with DCM (2×2 mL). The combined extracts were dried (MgSO4), and chromatographed on silica gel (0-8% 2 M methanolic ammonia/DCM), giving the title compound as a colorless oil (100 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07279491B2 |
| Source dataset | uspto-grants-2007_10 |
| ORD ID | ord-ecf25f6be0114d04995767e250578e7a |
| Source note | uspto-grants-2007_10 |