HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → HCID 131719732, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 131719733 | HCID 131719733 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 131719732 | HCID 131719732 | — |
Reaction Steps
A solution of 4-tert-butylcarbonyl-7α-methoxy-3-methyl-2-(1-methyl-1,2,3,4-tetrazol-5-yl)thio-3-cephem 1,1-dioxide (300 mg), prepared as described in PCT EP 90/02189 in dimethyl sulphoxide (3 ml), was treated at room temperature with triethylamine (0.110 ml) and methyl iodide (0.135 ml). After 1 hr, the reaction mixture was diluted with ethyl acetate, sequentially washed with a dilute solution of hydrochloric acid and brine and eventually dried over Na2SO4. Removal of the solvent and flash chromatography of the residue afforded the title compound as a white solid (160 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05580865 |
| Source dataset | uspto-grants-1996_12 |
| ORD ID | ord-2bd9316d06e046cd94da3c0b6f5e693d |
| Source note | uspto-grants-1996_12 |