HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-(N-Boc-amino)piperidine → HCID 86608431, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-(N-Boc-amino)piperidine | HCID 723833 | — |
| Reactant | 3,6-Dioxatricyclo[5.4.0.0,2,4]undeca-1(11),7,9-triene | HCID 13149033 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 86608431 | HCID 86608431 | — |
Reaction Steps
To 3 g of the compound obtained in Step B of Example 4, dissolved in 45 ml of acetonitrile, there are added 4 g of tert-butyl piperidin-4-ylcarbamate (20.2 mmol). The mixture is then heated at reflux for 12 hours and subsequently evaporated to dryness. A yellow oil is obtained which is purified by flash chromatography on silica (eluant: dichloromethane/ethanol 95/5) to yield the expected product in the form of a pale-yellow meringue.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07465733B2 |
| Source dataset | uspto-grants-2008_12 |
| ORD ID | ord-af751b25057342d699ad7c16b3583d90 |
| Source note | uspto-grants-2008_12 |