HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Benzylpiperazine → 1-Benzyl-4-[(1-t-butoxycarbonyl-4-piperidyl)carbonyl]piperazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Benzylpiperazine | HCID 75994 | — |
| Reactant | Succinimido 1-t-butoxycarbonylpiperidine-4-carboxylate | HCID 15578030 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-Benzyl-4-[(1-t-butoxycarbonyl-4-piperidyl)carbonyl]piperazine | HCID 4014625 | — |
Reaction Steps
N-Benzylpiperazine (40.0 ml) was added in one portion to a solution of succinimido 1-t-butoxycarbonylpiperidine-4-carboxylate (75.0 g) in dry dichloromethane (1600 ml). The solution was stirred at ambient temperature under an atmosphere of argon for 17 hours. The solution was washed with water (500 ml) and saturated brine (250 ml). The organic layer was dried (Na2SO4) and evaporated. The residual oil was purified by chromatography on alumina, eluting with dichloromethane to give 1-benzyl-4-[(1-t-butoxycarbonyl-4-piperidyl)carbonyl]piperazine as an oil;
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06090813 |
| Source dataset | uspto-grants-2000_07 |
| ORD ID | ord-5aa4818ba0ba4c588412a8deb95b3af8 |
| Source note | uspto-grants-2000_07 |