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HRID 1491521作成日:2026年10月24日

Sodium Iodide → 1,3-Dioxolan-2-one-4-yl 5-(N-acetylamino)-3-(N-acetyl-N-methylamino)-2,4,6-triiodobenzenecarboxylate

https://huagongshe.com/ja/reaction/1491521

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium IodideHCID 5238—
反応物4-Chloro-1,3-dioxolan-2-oneHCID 98075—
反応物potassium 5-(N-acetylamino)3-(N-acetyl-N-methylamino)-2,4,6-triiodobenzenecarboxylateHCID 23717801—
溶媒DimethylformamideHCID 6228—
生成物1,3-Dioxolan-2-one-4-yl 5-(N-acetylamino)-3-(N-acetyl-N-methylamino)-2,4,6-triiodobenzenecarboxylateHCID 19422764—

反応条件

温度50 °C

反応手順

4-Chloro-1,3-dioxolan-2-one (1.35 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 retool) and sodium iodide (0.15 g, 1 retool) in dry DMF (50 ml). 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 dissolved in chloroform (100 ml) and washed four times with a saturated sodium hydrogen carbonate solution and finally twice with water. After treatment with magnesium sulfate the solution was finally evaporated to dryness. Yield: 5.6 g. Purity by HPLC: 93%. 1H-NMR (DMSO-d6): delta=1.67 (N(CH3)COCH3); 2.05(NCOCH3); 2.96 (NCH3); 4.7; 4.9(CH2); 7.02(CH); 10.14 ppm (NH).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05370861
出典データセットuspto-grants-1994_12
ORD IDord-dab560ecceff48c9950e32dcf7b741d0
出典メモuspto-grants-1994_12