HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 57110108, compound → HCID 131721893, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 57110108 | HCID 57110108 | — |
| Reactant | HCID 131721894 | HCID 131721894 | — |
| Product | HCID 131721893 | HCID 131721893 | 83.4% |
Reaction Steps
By using 4-nitrobenzyl (1R,5R,6S)-6-[(1R)-1-hydroxyethyl]-1-methyl-2-diphenylphosphoryl-1-carbapen-2-em-3-carboxylate (1.78 g) and (2S,4S)-2-[(3S)-3-[3-hydroxy-4-(4-nitrobenzyloxycarbonyl)aminobutanoylamino]pyrrolidin-1-ylcarbonyl]-4-mercapto-1-(4-nitrobenzyloxycarbonyl)pyrrolidine (2.0 g), reaction and purification were carried out in a similar manner to that described in Example 1-(1), whereby 4-nitrobenzyl (1R,5S,6S)-6-[(1R)-1-hydroxyethyl]-2-[(2S,4S)-2-[(3S)-3-[3-hydroxy-4-(4-nitrobenzyloxycarbonyl)aminobutanoylamino]pyrrolidin-1-ylcarbonyl]-1-(4-nitrobenzyloxycarbonyl)pyrrolidin-4-ylthio]-1-methyl-1-carbapen-2-em-3-carboxylate (2.52 g) was obtained as an amorphous substance.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06090802 |
| Source dataset | uspto-grants-2000_07 |
| ORD ID | ord-9a415037b3be45e789da6a9b4be9cede |
| Source note | uspto-grants-2000_07 |