HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Acetate → 1-Acetyl-4-[3-(piperidin-1-yl)phenylamino]-piperidine dihydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | N-Acetyl-4-piperidone | HCID 122563 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | 1-(3-Aminophenyl)piperidine dihydrochloride | HCID 23366944 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-Acetyl-4-[3-(piperidin-1-yl)phenylamino]-piperidine dihydrochloride | HCID 23366900 | 132.1% |
Reaction Steps
To a solution of N-(3-aminophenyl)piperidine dihydrochloride (3.73 g) and 1-acetyl-4-piperidone (2.1 g) in methanol (30 ml) was added sodium cyano borohydride (1.9 g), followed by stirring at room temperature for 5 hours. To the mixture were added ethyl acetate ester (20 ml) and water (30 ml), the organic layer was dried over anhydrous sodium sulfate and then the solvent was distilled off. The residual oily compound was separated and purified by silica gel column chromatography (developing solvent: ethyl acetate ester). The oily compound was dissolved in dioxane (10 ml) and to the mixture was added 6N solution of hydrogen chloride in dioxane (2 ml). Then, the solvent was removed to obtain a colorless amorphous solid (3.7 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05580883 |
| Source dataset | uspto-grants-1996_12 |
| ORD ID | ord-3f0c13b8f65045b798b39ce173b37ba1 |
| Source note | uspto-grants-1996_12 |