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HRID 36785作成日:2026年10月26日
Potassium Iodide → 1-(Phenyloxycarbonyloxy)ethyl 5-(N-acetylamino)-3-(N-acetyl-N-methylamino)-2,4,6-triiodobenzenecarboxylate
https://huagongshe.com/reaction/36785
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Potassium Iodide | HCID 4875 | — |
| 反応物 | 1-Chloroethyl phenyl carbonate | HCID 13557093 | — |
| 反応物 | potassium 5-(N-acetylamino)3-(N-acetyl-N-methylamino)-2,4,6-triiodobenzenecarboxylate | HCID 23717801 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | 1-(Phenyloxycarbonyloxy)ethyl 5-(N-acetylamino)-3-(N-acetyl-N-methylamino)-2,4,6-triiodobenzenecarboxylate | HCID 19422759 | — |
反応手順
1-Chloroethyl phenyl carbonate (prepared according to Synthesis 1986, 627) (2.21 g, 11 mmol) was added at room temperature to a solution of potassium 5-(N-acetylamino)-3-(N-acetyl-N-methylamino)-2,4,6-triiodobenzenecarboxylate (6.66 g, 10 mmol) and potassium iodide (0.17 g, 1 mmol) in dry DMF. After stirring at 50° C. for 6 hours and at room temperature for 4 days the solvent was removed at reduced pressure. The residue was suspended in chloroform (100 ml) and washed four times with a saturated sodium hydrogen carbonate solution and twice with water. After drying with magnesium sulfate the solution was evaporated to dryness. Yield: 7.3 g. Purity by HPLC: 98%. 1H-NMR (DMSO-d6): delta=1.68 (N(CH3)COCH3); 1.74 (CHCH3); 2.05 (NCOCH3); 2.97 (NCH3); 7.05 (CH); 7.25-7.52 (arom.); 10.14 ppm (NH).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05416223 |
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| 出典データセット | uspto-grants-1995_05 |
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| ORD ID | ord-e23a9c7d5cff4733865868ed2fda8809 |
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| 出典メモ | uspto-grants-1995_05 |
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