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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1280134생성일: 2026년 10월 26일

Phosgene → N-[3-acetoxymethyl-5-(2,3-diacetoxypropylaminocarbonyl)-2,4,6-triiodophenyl]-N'[3,5-bis(2,3-diacetoxypropylaminocarbonyl)-2,4,6-triiodophenyl]urea

https://huagongshe.com/reaction/1280134

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참여 물질

역할이름HCID투입량
반응물PhosgeneHCID 6371—
반응물5-Amino-N,N'-bis(2,3-dihydroxypropyl)-2,4,6-triiodo-1,3-benzenedicarboxamide TetraacetateHCID 9897534—
반응물3-Acetoxymethyl-5-(2,3-diacetoxypropylaminocarbonyl)-2,4,6-triiodoanilineHCID 18429130—
촉매Hg(TFA)2HCID 16685285—
용매TolueneHCID 1140—
용매1,4-DioxaneHCID 31275—
생성물N-[3-acetoxymethyl-5-(2,3-diacetoxypropylaminocarbonyl)-2,4,6-triiodophenyl]-N'[3,5-bis(2,3-diacetoxypropylaminocarbonyl)-2,4,6-triiodophenyl]ureaHCID 18429324—

반응 조건

온도60 °C

반응 단계

3,5-Bis(2,3-diacetoxypropylaminocarbonyl)-2,4,6-triiodoaniline (260 mg, 0.30 mmol) was dissolved in dioxane (1.0 ml) and a solution of phosgene in toluene (1.93 M, 1.8 ml) was added. The flask was tightly sealed and then heated to 60° C. for 17 h. After cooling to room temperature, the solvent was distilled off at reduced pressure. Dioxane (3 ml) was added and distilled off again. This procedure was repeated twice. Dioxane (1 ml) was added followed by 3-acetoxymethyl-5-(2,3-diacetoxypropylaminocarbonyl)-2,4,6-triiodoaniline (0.245 g, 0.31 mmol), prepared according to Example 16a, and Hg(OCOCF3)2 (20 mg). The mixture was stirred for 16 h at room temperature, the solvent was evaporated and the residue was purified by preparative HPLC. Yield: 0.192 g (39%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06448442B1
출처 데이터셋uspto-grants-2002_09
ORD IDord-c521745d17b4445a83de0f5063969d20
출처 메모uspto-grants-2002_09