HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 86757194, compound → HCID 86757193, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 86757194 | HCID 86757194 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 86757193 | HCID 86757193 | 69% |
Reaction Steps
A solution of 0.15 g of (E)-2′-(3-aminopropanesulphonyl)-2(R)-[1(S)-(benzyloxycarbamoyl)-4-phenyl-3-butenyl]-2′-isobutyl-4-methylvalerohydrazide in 5 ml of methanol was hydrogenated in the presence of 60 mg of 10% palladium-on-charcoal until uptake of hydrogen was complete. The catalyst was removed by filtration and the solvent was evaporated. The residue was triturated with diethyl ether and there was obtained 0.088 g of 2′-(3-aminopropanesulphonyl)-2(R)-[1(S)-(hydroxycarbamoyl)-4-phenylbutyl]-2′-isobutyl-4-methylvalerohydrazide in the form of a pale pink solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06265446B1 |
| Source dataset | uspto-grants-2001_07 |
| ORD ID | ord-37cdaea86e6d4acc81871010f3f4f4f9 |
| Source note | uspto-grants-2001_07 |