HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 4-Amino-1-(1-benzyloxycarbonyl-4-piperidinylmethyl)piperidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 1-(1-Benzyloxycarbonyl-4-piperidinylmethyl)-4-(t-butoxycarbonylamino)piperidine | HCID 12986153 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-Amino-1-(1-benzyloxycarbonyl-4-piperidinylmethyl)piperidine | HCID 69830801 | 101.2% |
Reaction Steps
To a solution of 1-(1-benzyloxycarbonyl-4-piperidinylmethyl)-4-(t-butoxycarbonylamino)piperidine (7.77 g) in ethanol (30 ml) is added a 30% solution of hydrochloric acid in ethanol (15 ml) under ice-cooling, and the mixture is stirred at room temperature for 5 hours. The solvent is evaporated under reduced pressure, and the residue is dissolved in water. The solution is basified with potassium carbonate and extracted with chloroform. The extract is washed with a saturated aqueous sodium chloride solution, dried over anhydrous magnesium sulfate, and the solvent is evaporated under reduced pressure to give the desired compound (6.04 g) as an oily product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06294555B1 |
| Source dataset | uspto-grants-2001_09 |
| ORD ID | ord-7b9c5f06f1bc45fa965ecc36c4a14056 |
| Source note | uspto-grants-2001_09 |