HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 54378637, compound → HCID 53652743, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 54378637 | HCID 54378637 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Catalyst | iodoplatinate | HCID 170165 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 53652743 | HCID 53652743 | — |
Reaction Steps
A solution of 1.09 g (2.60 mmol) 1-(t-butylacetamido)-3-azido-5,7-diphenylhexahydroazepin-2-one in 30 mL ethanol and 15 mL methylene chloride was hydrogenated at 42 psi in the presence of 0.40 g 10% palladium-on-carbon for 36 hours. The reaction showed Rf 0.30/0.15 iodoplatinate positive, in 30% methanol in ethyl acetate. It was filtered through Celite with ethanol and methylene chloride, evaporated, and chromatographed on silica gel using 30% methanol in ethyl acetate as eluant to afford 300 mg (29%) of the less polar diastereomer as an oil and 420 mg (41%) of the more polar diastereomer as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05484917 |
| Source dataset | uspto-grants-1996_01 |
| ORD ID | ord-d5a49fc567be4958b3b7028bb4ef1fb4 |
| Source note | uspto-grants-1996_01 |