HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → HCID 178462280, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | 4-nitrobenzyl (1S,5R,6S)-6-((1R)-1-hydroxyethyl)-2-(imidazo[5,1-b]thiazol-3-yl)-1-methyl-1-carbapen-2-em-3-carboxylate | HCID 131722901 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 178462280 | HCID 178462280 | — |
Reaction Steps
To a suspension of 102 mg of 4-nitrobenzyl (1S,5R,6S)-6-((1R)-1-hydroxyethyl)-2-(imidazo[5,1-b]thiazol-3-yl)-1-methyl-1-carbapen-2-em-3-carboxylate 1.5 ml of dry dichloromethane was added 2.7 ml of iodomethane, and the mixture was stirred under the atmosphere of argon in the darkness at room temperature for 3 days. Unreacted reagent was removed under reduced pressure to give 122 mg of 4-nitrobenzyl (1S,5R,6S)-6-((1R)-1-hydroxyethyl)-1-methyl-2-(6-methylimidazo[5,1-b]thiazolium-3-yl)-1-carbapen-2-em-3-carboxylate iodide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06310056B1 |
| Source dataset | uspto-grants-2001_10 |
| ORD ID | ord-a5a2537e7e7949178d244984a9e795a9 |
| Source note | uspto-grants-2001_10 |