HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Phenylpiperazine → 1-(N-Benzyloxycarbonyltyrosyl)-4-phenylpiperazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Phenylpiperazine | HCID 7096 | — |
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | N-benzyloxycarbonyl-l-tyrosine | HCID 712438 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-(N-Benzyloxycarbonyltyrosyl)-4-phenylpiperazine | HCID 54463856 | 58.6% |
Reaction Steps
12.3 g of N-benzyloxycarbonyltyrosine and 6.6 g of N-phenylpiperazine were dissolved in 150 ml of methylene chloride, and to the solution was added 8.4 g of DCC, and the mixture was stirred at a room temperature for 5 hours. Precipitated insoluble matter was filtered off and the filtrate was concentrated under a reduced pressure, and resulting residue was applied to a silica gel column and eluted with hexane/ethyl acetate (1:1 to 1:2) to obtain 10.5 g of the title compound in a colorless amorphous form.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05245034 |
| Source dataset | uspto-grants-1993_09 |
| ORD ID | ord-6fb0cb4113fb499eb4dfc30867774f34 |
| Source note | uspto-grants-1993_09 |