HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 19969545, compound → HCID 19969562, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 19969545 | HCID 19969545 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | HCID 178418390 | HCID 178418390 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 19969562 | HCID 19969562 | 43% |
Reaction Steps
0.80 g of 10% palladium-carbon was added to 30 ml of a solution of 1.56 g of (3RS,6SR)-3-(benzothiazol-2-yl)carbamoyl-3-benzyl-1-benzyloxy-6-isobutylpipera- zine-2,5-dione in dioxane. The mixture was stirred at room temperature for 4 hours in a hydrogen current. The reaction mixture was filtered to remove the catalyst. The filtrate was subjected to distillation to remove the solvent. The resulting light brown oily substance was recrystallized using dichloromethane, to obtain 0.56 g of (3RS,6SR)-3-(benzothiazol-2-yl)carbamoyl-3-benzyl-1-hydroxy-6-isobutylpiperazine-2,5-dione.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05607934 |
| Source dataset | uspto-grants-1997_03 |
| ORD ID | ord-22c19ba805ff43ecb77ff6656d24c5c7 |
| Source note | uspto-grants-1997_03 |