HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dicyclohexylcarbodiimide → 1-[2-(Benzyloxycarbonylamino)-3-hydroxypropionyl]-4-(3-phenylpropyl)piperazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | N-(Benzyloxycarbonyl)-L-serine | HCID 100310 | — |
| Reactant | 1-(3-Phenylpropyl)piperazine | HCID 796534 | — |
| Reactant | HCID 178527226 | HCID 178527226 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 1-[2-(Benzyloxycarbonylamino)-3-hydroxypropionyl]-4-(3-phenylpropyl)piperazine | HCID 14881549 | 73.1% |
Reaction Steps
Dicyclohexylcarbodiimide (1.58 g) was added to an ice-cooled solution of 2.0 g of N-carbobenzyloxyserine, 1.57 g of 1-(3-phenylpropyl)piperazine and 1.04 g of 1-hydroxybenzotiazole in 30 ml of N,N-dimethylformamide. The mixture was stirred at room temperature for 24 hours, then diluted with ethyl acetate, washed in sequence with two portions of 4% aqueous sodium hydrogen carbonate, one portion of water and one portion of saturated aqueous solution of sodium chloride, dried over anhydrous sodium sulfate and concentrated under reduced pressure. The residue was purified by silica gel column chromatography to give 2.39 g of 1-[2-(benzyloxycarbonylamino)-3-hydroxypropionyl]-4-(3-phenylpropyl}piperazine. Melting point 95°-97° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04987132 |
| Source dataset | uspto-grants-1991_01 |
| ORD ID | ord-3046f51986a644cea6a3ac80c2e3dd47 |
| Source note | uspto-grants-1991_01 |