HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide →
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | HCID 86750477 | HCID 86750477 | — |
| Solvent | Acetone | HCID 180 | — |
Reaction Steps
To a solution of allyl (4R,5S,6S)-3-[(2R,4S)-1-allyloxycarbonyl-2-(1-methylimidazol-2-ylmethyl)-pyrrolidin-4-yl]thio-6-[(1R)-1-hydroxyethyl ]-4-methyl-7-oxo-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylate (1.25 g) in acetone (12 ml) was added methyl iodide (1.47 ml ) at room temperature. The mixture was stirred for 35 hours at the same temperature. The reaction mixture was evaporated in vacuo to give allyl (4R,5S,6S)-3-[(2R,4S)-1-allyloxycarbonyl-2-(1, 3-dimethyl-2-imidazoliomethyl)-pyrrolidin-4-yl]thio-6-[(1R)-1-hydroxyethyl]-4-methyl-7-oxo-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylate iodide (1.49 g) as an amorphous solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05608056 |
| Source dataset | uspto-grants-1997_03 |
| ORD ID | ord-417d3e155aa044a6a6ff666de2de94ba |
| Source note | uspto-grants-1997_03 |