首页> 外国专利> Production manner of the sulfonic acid ester of N aryl methyl - ethanolamine as a 1,4,7,10 tetoraazashikurododekan derivative, and the intermediate field which are obtained from the N aryl methyl - aziridine derivative and the aforementioned derivative

Production manner of the sulfonic acid ester of N aryl methyl - ethanolamine as a 1,4,7,10 tetoraazashikurododekan derivative, and the intermediate field which are obtained from the N aryl methyl - aziridine derivative and the aforementioned derivative

机译:由N芳基甲基-氮丙啶衍生物和上述衍生物获得的作为1,4,7,10 tetoraazashikurododekan衍生物的N芳基甲基-乙醇胺磺酸酯的制备方法和中间场

摘要

(57) Abstract As for the aziridine receiving the annular oligomer conversion reaction, when preparing the chelation medicine in order to use for example as the contrast material of image diagnostics the usefulness, it is possible to generate poriazashikuroarukan chemical compound. Especially, when N-benjiru-ajirijin converts, annular four quantitative embody and the deviation from to benzyl preparing the chelation medicine it is useful as generates shikuren which is the intermediate field. This invention, formula (i) (however, as for R1, independently, to be hydrogen or Ar, as for Ar it is phenyl group displacement with option.)It shows, N-benjiru-ajirijin and other N-ariru methyl - the aziridine it is something which offers especially the attractive root in order to produce, this production manner the N-ariru methyl which was refined - includes the fact that it reacts the sulfonic acid ester of ethanolamine with the base. The N-ariru methyl which is the intermediate field - the sulfonic acid ester of ethanolamine is displayed with the formula, R''NHCH2 CH2 OSO3 H, it is the aryl methyl group R''ga N- (bis aryl methyl) basis or the N- (triallyl methyl) basis of Order n. In addition, another edge strip of this invention is something which offers the chemical compound formula (ii). However, as for Ar and R1 when it defined first, it is similar, the ArCHR1 section where two differs at least exists.
机译:(57)<摘要>对于接受环状低聚物转化反应的氮丙啶,在制备螯合药物以例如用作图像诊断的对比材料的有用性时,有可能生成po杂黑呋喃化合物。尤其是,当N-本杰鲁-阿吉里津转化时,环状的四个定量体现和与苄基的偏差制备了螯合药物,它可用作产生中间体的shikuren。本发明的式(i)(但是,R 1 分别独立地为氢或Ar,Ar可选地为苯基取代)。和其他N-ariru甲基-氮丙啶是一种特别具有吸引力的根,以便生产,这种生产方式经过精制的N-ariru甲基-包括它使乙醇胺的磺酸酯与碱反应的事实。 N-ariru甲基是中间区域-乙醇胺的磺酸酯,其化学式为R''NHCH 2 CH 2 OSO 3 < H是n阶的芳基甲基R” ga N-(双芳基甲基)基或N-(三烯丙基甲基)基。另外,本发明的另一种边缘条是提供化学式(ii)的物质。但是,首先定义的Ar和R 1 相似,至少存在两个不同的ArCHR 1 部分。

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