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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1613026생성일: 2026년 10월 27일

Sodium Carbonate → N,N'-Bis[(2,3-dihydroxypropyl)-2-hydroxyethyl]-5-hydroxyacetamido-2,4,6-triiodoisophthalamide

https://huagongshe.com/reaction/1613026

반응식

참여 물질

역할이름HCID투입량
반응물Sodium CarbonateHCID 10340—
반응물5-[[2-(Acetyloxy)acetyl]amino]-2,4,6-triiodo-1,3-benzenedicarbonyl dichlorideHCID 12943191—
반응물3-[(2-Hydroxyethyl)amino]propane-1,2-diolHCID 15034945—
반응물5-Acetoxyacetamido-N,N'-bis[(2,3-dihydroxypropyl)-2-hydroxyethyl]-2,4,6-triiodoisophthalamideHCID 86745331—
용매DimethylacetamideHCID 31374—
용매Dichloromethane ethylacetateHCID 21226138—
생성물N,N'-Bis[(2,3-dihydroxypropyl)-2-hydroxyethyl]-5-hydroxyacetamido-2,4,6-triiodoisophthalamideHCID 8674533086%

반응 단계

5-Acetoxyacetamido-N,N'-bis[(2,3-dihydroxypropyl)-2-hydroxyethyl]-2,4,6-triiodoisophthalamide. 69 g (0.1 g-mole) of 5-acetoxyacetamido-2,4,6-triiodoisophthaloyl chloride is dissolved in DMAc (140 ml) and anhydrous Na2CO3 (31.8 g, 0.3 g-mole) is added. To the solution, a DMAc solution (87 ml) containing 26.2 g (0.3 g-mole) of 3-(N-2-hydroxyethyl)amino-1,2-propanediol is added. The mixture is heated and stirred at 35°-40° C. until the reaction is completed as determined by the TLC analysis (EtOAc/CH2Cl2 ; 30/20). After the reaction, the inorganic salts are filtered and the filtrate containing the desired product is evaporated to dryness to give a gum. The gum is triturated with isopropyl alcohol to dissolve the excess amino-triol. The clear supernatant is decanted and the residual solid is dissolved in water (150 ml), treated with Amberlite® IR-120H resin and evaporated to dryness to give the desired product (77 g, 86% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05191120
출처 데이터셋uspto-grants-1993_03
ORD IDord-c9182094a13a4c148242f82ef5717257
출처 메모uspto-grants-1993_03