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HRID 745968作成日:2026年10月26日
Water → (2-methoxy-2-methylpropanoyl)oxymethyl (6R,7R)-3-(carbamoyloxymethyl)-7-[[(2Z)-2-(furan-2-yl)-2-methoxyiminoacetyl]amino]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate
https://huagongshe.com/reaction/745968
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Water | HCID 962 | — |
| 反応物 | Potassium Carbonate | HCID 11430 | — |
| 反応物 | Cefuroxime | HCID 5479529 | — |
| 反応物 | Iodomethyl 2-methoxy-2-methylpropanoate | HCID 22145393 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | (2-methoxy-2-methylpropanoyl)oxymethyl (6R,7R)-3-(carbamoyloxymethyl)-7-[[(2Z)-2-(furan-2-yl)-2-methoxyiminoacetyl]amino]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate | HCID 13478066 | 69.1% |
反応手順
Cefuroxime (1.697 g) and powdered potassium carbonate (276 mg) were stirred in anhydrous N,N-dimethylformamide (20 ml) at 22° for 1 hour and the resulting solution was cooled in an ice/salt bath to -8°. A solution of crude 2-methoxy-2-methylpropanoic acid iodomethyl ester (1.52 g) in anhydrous N,N-dimethylformamide (6 ml) was added and the solution was stirred for 35 mins. Water (75 ml) was added and the mixture was extracted with ethyl acetate (2×100 ml). The combined organic layers were washed successively with 50 ml each of 2N hydrochloric acid (3×), water, saturated aqueous sodium bicarbonate, water, 10% aqueous sodium metabisulphite, water (2×) and saturated brine, dried over magnesium sulphate and concentrated under vacuum to ca 10 ml. The solution was added dropwise to stirred petroleum ether (100 ml) to give a precipitate which was filtered off, washed with petroleum ether and dried under reduced pressure to give the title ester (1.532 g); λmax (ethanol 277) nm E11 323; νmax (CHBr3) 3520 and 3400 (NH and NH2), 1788 (β-lactam C=O); 1735 (ester and carbamate C=O) and 1685 and 1510 cm-1 (amide C=O).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04602012 |
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| 出典データセット | uspto-grants-1986_07 |
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| ORD ID | ord-58a710ae07af42bb9c02a77b1ef85639 |
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| 出典メモ | uspto-grants-1986_07 |
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