HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → HCID 178459475, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | HCID 131722292 | HCID 131722292 | — |
| Product | HCID 178459475 | HCID 178459475 | 98.9% |
Reaction Steps
Iodomethane (1.00 g) is added to 43.2 mg of allyl(1R,5S,6S)-2-[(3S,5S)-1-allyloxycarbonyl-5-[(imidazo[5,1-b]thiazol-5-yl)methylaminocarbonyl]pyrrolidin-3-yl]thio-6-((1R)-1-hydroxyethyl)-1-methylcarbapen-2-em-3-carboxylate, and the mixture is allowed to stand in an argon atmosphere in a light-shielded state at room temperature for 19 hr. The excess reagent is removed by evaporation under reduced pressure to give 52.6 mg of allyl(1R,5S,6S)-2-[(3S,5S)-1-allyloxycarbonyl-5-[(6-methylimidazo[5,1-b]thiazolium-5-yl)methylaminocarbonyl]pyrrolidin-3-yl]thio-6-((1R)-1-hydroxyethyl)-1-methylcarbapen-2-em-3-carboxylate iodide as a slightly yellowish solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06180622B2 |
| Source dataset | uspto-grants-2001_01 |
| ORD ID | ord-d5679ed7feae4d129373c00d26877106 |
| Source note | uspto-grants-2001_01 |