HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 22837343, compound → HCID 22837345, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 22837343 | HCID 22837343 | — |
| Reactant | HCID 86742066 | HCID 86742066 | — |
| Product | HCID 22837345 | HCID 22837345 | — |
Reaction Steps
According to a similar procedure to that described in Example 1(l), t-butyl α-[3(S*)-amino-6(R*)-(p-fluorophenyl)-2-oxoperhydroazepin-1-yl]acetate [prepared as described in Example 6(e)] was reacted with butyl 4-phenyl-2(R)-trifluoromethanesulfonyloxybutyrate, to give a crude product, which was subjected to column chromatography through silica gel using a 3:1 by volume mixture of cyclohexane and ethyl acetate as eluent.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04734410 |
| Source dataset | uspto-grants-1988_03 |
| ORD ID | ord-fd64dfa5e9904d1bacc74f2b0a025850 |
| Source note | uspto-grants-1988_03 |