HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 15200286, compound → HCID 57291756, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 15200286 | HCID 15200286 | — |
| Reactant | HCID 57074623 | HCID 57074623 | — |
| Reactant | HCID 131718807 | HCID 131718807 | — |
| Product | HCID 57291756 | HCID 57291756 | — |
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 (290 mg, 0.49 mmol) and (2S,4S)-2-[2-carbamoyl-N-(p-nitrobenzyloxycarbonyl)pyrrolidin-4-yl]-4-mercapto-N-(p-nitrobenzyloxycarbonyl)pyrrolidine diastereomer II (280 mg, 0.49 mmol, compound of Reference Example 14) to obtain p-nitrobenzyl (1R,5S,6S)-2-[(2S,4S)-2-[2-carbamoyl-N-(p-nitrobenzyloxycarbonyl)pyrrolidin-4-yl]-N-(p-nitrobenzyloxycarbonyl)pyrrolidin-4-ylthio]-6-[(R)-1-hydroxyethyl]-1-methyl-1-carbapen-2-em-3-carboxylate diastereomer II (419 mg, yield: 93.4%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05438054 |
| Source dataset | uspto-grants-1995_08 |
| ORD ID | ord-ff78b557f46c46c0858e8ff8426d806d |
| Source note | uspto-grants-1995_08 |