HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyclohexane → t-Butyl rel-alpha-[3(S)-(8-t-butoxycarbonylamino-1-ethoxycarbonyloctylamino)-2-oxo-6(R)-phenylperhydroazepin-1-yl]acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyclohexane | HCID 8078 | — |
| Reactant | t-butyl rel-alpha-[3(S)-amino-2-oxo-6(R)-phenylperhydroazepin-1-yl]acetate | HCID 14003452 | — |
| Reactant | HCID 21287862 | HCID 21287862 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | t-Butyl rel-alpha-[3(S)-(8-t-butoxycarbonylamino-1-ethoxycarbonyloctylamino)-2-oxo-6(R)-phenylperhydroazepin-1-yl]acetate | HCID 22840211 | — |
Reaction Steps
1.2 g of t-butyl rel-α-[3(S)-amino-2-oxo-6(R)-phenylperhydroazepin-1-yl]acetate was treated with 2.15 g of ethyl 2-bromo-9-t-butoxycarbonylaminononanoate prepared as described in Preparation 4) in a similar manner to that described in Example 4, to afford a reaction product, which was subjected to column chromatography through silica gel using a mixture of cyclohexane and ethyl acetate in the ratio of 1:1 by volume as the eluent.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04778790 |
| Source dataset | uspto-grants-1988_10 |
| ORD ID | ord-325d7bd5fabc4ea5a8f6387f5204d9ab |
| Source note | uspto-grants-1988_10 |