HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 15200286, compound → HCID 15200292, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 15200286 | HCID 15200286 | — |
| Reactant | HCID 15200299 | HCID 15200299 | — |
| Product | HCID 15200292 | HCID 15200292 | 88.3% |
Reaction Steps
The same procedure as in Example 1-1 was carried out by using p-nitrobenzyl (1R,5S,6S)-2-diphenoxyphosphoryloxy-6-[(R)-1-hydroxyethyl]-1-methyl-1-carbapen-2-em-3-carboxylate (1.27 g, 2.14 mmol) and (2S,4S)-4-mercapto-N-(p-nitrobenzyloxycarbonyl)-2-[N-(p-nitrobenzyloxycarbonyl)pyrrolidin-3-yl]pyrrolidine diastereomer B (1.14 g, 2.15 mmol, compound of Reference Example 16) to obtain p-nitrobenzyl (1R,5S,6S)-6-[(R)-1-hydroxyethyl]-1-methyl-2-[(2S,4S)-N-(p-nitrobenzyloxycarbonyl)-2-[N-(p-nitrobenzyloxycarbonyl)pyrrolidin-3-yl]pyrrolidin-4ylthio]-1-carbapen-2-em-3-carboxylate diastereomer B (1.65 g, yield: 88.3%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05374720 |
| Source dataset | uspto-grants-1994_12 |
| ORD ID | ord-9af0926729204e31bb154013cc99d503 |
| Source note | uspto-grants-1994_12 |