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 | — |
| Product | HCID 57291756 | HCID 57291756 | 76.3% |
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 (185 mg, 0.31 mmol) and (2S,4S)-2-[2-carbamoyl-N-(p-nitrobenzyloxycarbonyl)pyrrolidin-4-yl]-4-mercapto-N-(p-nitrobenzyloxycarbonyl)pyrrolidine diastereomer III (175 mg, 0.31 mmol, compound of Reference Example 33) 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 (218 mg, yield: 76.3%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05438054 |
| Source dataset | uspto-grants-1995_08 |
| ORD ID | ord-1a6e7706c14d4de2a74b2c98c4a8efb2 |
| Source note | uspto-grants-1995_08 |