HuagongsheHuagongshe Chemistry Print Report · For research reference only
t-Butyl alpha-[3(S*)-azido-2-oxo-6(R*)-phenylperhydroazepin-1-yl]acetate → t-Butyl alpha-[3(S*)-amino-2-oxo-6(R*)-phenylperhydroazepin-1-yl]acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | t-Butyl alpha-[3(S*)-azido-2-oxo-6(R*)-phenylperhydroazepin-1-yl]acetate | HCID 14003443 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | t-Butyl alpha-[3(S*)-amino-2-oxo-6(R*)-phenylperhydroazepin-1-yl]acetate | HCID 14003450 | — |
Reaction Steps
0.3 g of 5% w/w palladium-on-carbon was added to 30 ml of ethanol containing 1.4 g of t-butyl α-[3(S*)-azido-2-oxo-6(R*)-phenylperhydroazepin-1-yl]acetate (Isomer A) [prepared as described in Example 1(h)], and under one atmosphere pressure of hydrogen the reaction mixture was shaken for 4 hours at 40° C. The catalyst was filtered off and the solvent was evaporated under reduced pressure, to give 1.56 g of the title compound as a gummy substance.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04734410 |
| Source dataset | uspto-grants-1988_03 |
| ORD ID | ord-937c9b542ff5470289cf2296ca2abbce |
| Source note | uspto-grants-1988_03 |