HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tert-butyl 3-(tert-butylcarbamoyl)piperazine-1-carboxylate → 1-Piperazinecarboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tert-butyl 3-(tert-butylcarbamoyl)piperazine-1-carboxylate | HCID 4063013 | — |
| Reactant | (2S,3S)-1,2-Epoxy-3-(Cbz-amino)-4-phenylbutane | HCID 9861019 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | 1-Piperazinecarboxamide | HCID 258192 | — |
Reaction Steps
0.395 g of 4-(tert.butoxycarbonyl)-N-tert.butyl-2-piperazinecarboxamide was dissolved in 50 ml of dry isopropanol and treated with 0.413 g of 3(S)-(benzyloxyformamido)-1,2(S)-epoxy-4-phenylbutane. The mixture was stirred at room temperature for 72 hours. The solvent was removed by evaporation to give a brown semi-solid material which was purified by flash chromatography on silica gel using 5% methanol in dichloromethane for the elution. There was obtained 0.234 g of 1-[3(S)-(benzyloxyformamido)-2(R)-hydroxy-4-phenylbutyl]-4-(tert.butoxycarbonyl)-N-tert.butyl-2(R or S)-piperazinecarboxamide as a mixture of diastereomers.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05620987 |
| Source dataset | uspto-grants-1997_04 |
| ORD ID | ord-c7b15625057f47b2ab0684bbedde28e0 |
| Source note | uspto-grants-1997_04 |