Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | N-methyl-N-(trimethylsilyl)trifluoroacetamide | HCID 32510 | — |
| Reactant | Trimethylsilyl iodide | HCID 85247 | — |
| Reactant | 7beta-[2-(2-Aminothiazol-4-yl)-2-(4-chlorobenzyloxyimino)acetamido]-3-acetoxymethyl-3-cephem-4-carboxylic acid | HCID 131715275 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-Iodomethylcephem | HCID 69068203 | — |
Reaction Steps
To a suspension of 200 mg (0.35 mmole) of 7β-[2-(2-aminothiazol-4-yl)-2-(4-chlorobenzyloxyimino)acetamido]-3-acetoxymethyl-3-cephem-4-carboxylic acid in 5 ml of methylene chloride was added 0.5 ml of MSTFA and the suspension was stirred at 40° C. until solution occurred. The solution was cooled to room temperature and 0.13 ml (0.87 mmole) of TMSI was added. The reaction stirred at room temperature for 30 minutes and evaporated to an oil. The oil was dissolved in 3 ml of acetonitrile and 0.12 ml (1.5 mmole) of THF was added. The mixture was then stirred at room temperature for 5 minutes to destroy excess TMSI and provide in solution the corresponding 3-iodomethyl-3-cephem derivative.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04698338 |
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| Source dataset | uspto-grants-1987_10 |
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| ORD ID | ord-a70f58c51dbe4e83bb5f58d4dea3b94d |
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| Source note | uspto-grants-1987_10 |
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