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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 36784생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/36784

반응식

참여 물질

역할이름HCID투입량
반응물Sodium IodideHCID 5238—
반응물4-Chloro-1,3-dioxolan-2-oneHCID 98075—
반응물potassium 5-(N-acetylamino)3-(N-acetyl-N-methylamino)-2,4,6-triiodobenzenecarboxylateHCID 23717801—
용매DimethylformamideHCID 6228—
생성물1,3-Dioxolan-2-one-4-yl 5-(N-acetylamino)-3-(N-acetyl-N-methylamino)-2,4,6-triiodobenzenecarboxylateHCID 19422764—

반응 조건

온도50 °C

반응 단계

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 mmol) and sodium iodide (0.15 g, 1 mmol) 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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05416223
출처 데이터셋uspto-grants-1995_05
ORD IDord-274ce378302f483fbc524d45a183068a
출처 메모uspto-grants-1995_05