関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Propanoic acid, 3-iodo- | HCID 8856 | — |
| 反応物 | Dicyclohexylcarbodiimide | HCID 10868 | — |
| 反応物 | 4-Pyrrolidinopyridine | HCID 75567 | — |
| 反応物 | Rhizoxin | HCID 6437358 | — |
| 溶媒 | Toluene | HCID 1140 | — |
| 生成物 | Rhizoxin 3-iodopropionate | HCID 86748167 | 80.7% |
反応手順
1.03 g of DCC and a catalytic amount of 4-pyrrolidinopyridine were added to a solution of 1.25 g of rhizoxin and 1.20 g of 3-iodopropionic acid in toluene, and the resulting mixture was stirred at room temperature for 2 hours. At the end of this time, the reaction mixture was treated in the same manner as described in Example 1, to give 1.33 g of rhizoxin 3-iodopropionate. The whole of this ester was immediately dissolved in 20 ml of acetonitrile, and 0.92 g of the silver salt of methylmercaptan prepared at the time of use was added. The resulting mixture was stirred at room temperature for 8 hours, after which the precipitate was filtered off. The solvent was then removed by distillation under reduced pressure, and ethyl acetate was added to the residue. The resulting mixture was washed with a 5% w/v aqueous solution of sodium bicarbonate and with a saturated aqueous solution of sodium chloride, in that order, after which it was dried over anhydrous sodium sulfate. The solvent was then removed by distillation under reduced pressure, and the residue was purified by silica gel column chromatography, using a 1:1 by volume mixture of cyclohexane and ethyl acetate as eluent, to give 970 mg of the title product.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05391564 |
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| 出典データセット | uspto-grants-1995_02 |
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| ORD ID | ord-745364b5b29043b39a34a52823d2783a |
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| 出典メモ | uspto-grants-1995_02 |
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