HuagongsheHuagongshe Chemistry Print Report · For research reference only
Iodoacetamide → HCID 15056108, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Iodoacetamide | HCID 3727 | — |
| Reactant | HCID 15056072 | HCID 15056072 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 15056108 | HCID 15056108 | 73.1% |
Reaction Steps
To a solution of 4-nitrobenzyl (4R,5S,6S)-6-[(1R)-1-hydroxyethyl]-3-[(2S,4S)-1-(4-nitrobenzyloxycarbonyl)-2-(pyrrolidin-1 -yl)methylpyrrolidin-4-yl]thio-4-methyl-7-oxo-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylate (0.77 g) in acetone (8 ml) was added iodoacetamide (0.93 g) at ambient temperature. The mixture was stirred overnight at the same temperature. The reaction mixture was evaporated in vacuo to give 4-nitrobenzyl (4R,5S,6S)-6-[(1R)-1-hydroxyethyl]-3-[(2S,4S)-2-(1-carbamoylmethylpyrrolidinio)methyl-1-(4-nitrobenzyloxycarbonyl)pyrrolidin-4-yl]thio-4-methyl-7-oxo-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylate iodide (0.71 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04925838 |
| Source dataset | uspto-grants-1990_05 |
| ORD ID | ord-2cd2c402e408478f869ac7e28f8a4994 |
| Source note | uspto-grants-1990_05 |