HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Sulfanylpyrrolidin-2-one → 4-Nitrobenzyl (1R,5S,6S)-2-[(RS)-5-oxo-3-pyrrolidinylthio]-6-[1(R)-hydroxyethyl]-1-methyl-1-carbapen-2-em-3-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Sulfanylpyrrolidin-2-one | HCID 10129935 | — |
| Reactant | HCID 57036270 | HCID 57036270 | — |
| Product | 4-Nitrobenzyl (1R,5S,6S)-2-[(RS)-5-oxo-3-pyrrolidinylthio]-6-[1(R)-hydroxyethyl]-1-methyl-1-carbapen-2-em-3-carboxylate | HCID 57208216 | 59% |
Reaction Steps
Following a procedure similar to that described in Example 27(b), but using 4-nitrobenzyl (1R,5S,6S)-2-(2-diethylcarbamoylphenylsulfinyl)-1-methyl-6-[1(R)-hydroxyethyl]-1-carbapen-2-em-3-carboxylate [prepared as described in Example 27(a)] and 4-mercapto-2-oxopyrrolidine as starting materials, in relative proportions similar to those used in that Example, the title compound was obtained as a powder in a yield of 59%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05719275 |
| Source dataset | uspto-grants-1998_02 |
| ORD ID | ord-ba5a63acf9f543e2b81de40aa8147ea4 |
| Source note | uspto-grants-1998_02 |