方法以5-氨基-2，4，6-三碘异酞酸为原料经酰氯化、酰胺化反应制得目标化合物。
METHODS The title compound was synthesized from 5-amino-2,4, -6-triiodoisophthalic acid by acyl chlorination and amidation.
方法以5-氨基-2，4，6-三碘异酞酸为原料经酰氯化、酰胺化反应制得目标化合物。
METHODS The title compound was synthesized from 5-amino-2,4, -6-triiodoisophthalic acid by acyl chlorination and amidation.
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