HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1195545Generated: October 30, 2026
Diisopropyl Ether → Sodium 7-[2-(2-aminothiazol-4-yl)-2-methoxyiminoacetamido]-3-vinyl-3-cephem-4-carboxylate
https://huagongshe.com/reaction/1195545
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diisopropyl Ether | HCID 7914 | — |
| Reactant | Iodomethyl pivalate | HCID 104401 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 7-[2-(2-Aminothiazol-4-yl)-2-methoxyimino-acetamido]-3-vinyl-3-cephem-4-carboxylic acid | HCID 131713168 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Sodium 7-[2-(2-aminothiazol-4-yl)-2-methoxyiminoacetamido]-3-vinyl-3-cephem-4-carboxylate | HCID 131713178 | — |
| Product | Pivaloyloxymethyl 7-[2-(2-aminothiazol-4-yl)-2-methoxyiminoacetamido]-3-vinyl-3-cephem-4-carboxylate | HCID 131713179 | — |
Reaction Steps
Sodium 7-[2-(2-aminothiazol-4-yl)-2-methoxyiminoacetamido]-3-vinyl-3-cephem-4-carboxylate (syn isomer) (2.9 g), which was prepared from 7-[2-(2-aminothiazol-4-yl)-2-methoxyiminoacetamido]-3-vinyl-3-cephem-4-carboxylic acid and sodium bicarbonate in substantially the same manner as that of Example 78-(1), was dissolved in N,N-dimethylformamide (30 ml), and thereto was added dropwise a solution of iodomethyl pivalate (1.62 g) in N,N-dimethylformamide (5 ml) under ice-cooling with stirring, and the stirring was continued at the same temperature for 10 minutes. To the reaction mixture were added ethyl acetate 200 ml) and water (150 ml), followed by separating out the organic layer, which was washed with a saturated aqueous solution of sodium bicarbonate and an aqueous solution of sodium chloride, and then dried over anhydrous magnesium sulfate. Removal of the solvent gave an oil, which was pulverized with diisopropyl ether to obtain pivaloyloxymethyl 7-[2-(2-aminothiazol-4-yl)-2-methoxyiminoacetamido]-3-vinyl-3-cephem-4-carboxylate (syn isomer) (2.1 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05110921 |
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| Source dataset | uspto-grants-1992_05 |
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| ORD ID | ord-e936c1bcce864a739404c1ba2c92bd4f |
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| Source note | uspto-grants-1992_05 |
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