Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | HCID 91285261 | HCID 91285261 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 69364166 | HCID 69364166 | — |
Reaction Steps
4-Nitrobenzyl (1S,5R,6S)-6-((1R)-1-hydroxyethyl)-1-methyl-2-[7-(quinolin-3-yl)carbonylimidazo[5,1-b]-thiazol-2-yl]-1-carbapen-2-em-3-carboxylate (93 mg) was dissolved in acetonitrile (2.25 ml)/chloroform (0.75 ml) to prepare a solution. Methyl iodide (0.063 ml) was added to the solution at room temperature, and the mixture was stirred at 40° C. for 3 days. The reaction solution was poured into diethyl ether to produce a powder which was filtered to give an N-quaternarized compound. The title compound (7.7 mg) was prepared in substantially the same manner as in step b) of Example 1, except that this compound was used as the starting compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06908913B2 |
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| Source dataset | uspto-grants-2005_06 |
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| ORD ID | ord-e8437ca43e454e43bb22bc278b55e3f9 |
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| Source note | uspto-grants-2005_06 |
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