HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide →
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Diisopropyl Ether | HCID 7914 | — |
| Reactant | HCID 131714636 | HCID 131714636 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
Reaction Steps
A mixture of benzhydryl 7-tert-butoxycarbonylamino-3-[2-(2-pyridyl)thiovinyl]-3-cephem-4-carboxylate (trans isomer) (5.0 g) N,N-dimethylformamide (25 ml) and methyl iodide (5 ml) was allowed to stand for 9 days at ambient temperature. The reaction mixture was poured into diisopropyl ether and the resultant oily residue was triturated with ethyl acetate and collected by filtration to give benzhydryl 7-tert-butoxycarbonylamino-3-[2-(1-methyl-2-pyridinio)thiovinyl]-3-cephem-4-carboxylate iodide (trans isomer) (5.2 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04584290 |
| Source dataset | uspto-grants-1986_04 |
| ORD ID | ord-a14b7e5c20f64be7b7a108530f295a65 |
| Source note | uspto-grants-1986_04 |