A New Contrast Agent of Triiodobenzene Compounds

The technology of a compound and a contrast agent is applied in the field of triiodobenzene compound and a contrast agent containing the compound, 5--N, and can solve the problems of high viscosity, toxicity and hypertonicity, etc.

Active Publication Date: 2011-12-14
ZHEJIANG STARRY PHARMA
View PDF4 Cites 1 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0003] Clinical studies have found that the above-mentioned three types of iodine contrast agents all have one or another disadv

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • A New Contrast Agent of Triiodobenzene Compounds
  • A New Contrast Agent of Triiodobenzene Compounds
  • A New Contrast Agent of Triiodobenzene Compounds

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 15

[0026] Example 15-(N-methylacetylamino)-N, N'-bis(2,3-dihydroxy-n-propyl)-2,4,6-triiodoisophthalamide (I)

[0027]

[0028] Under ice-water bath cooling and mechanical stirring, 5-(acetylamino)-N,N'-bis(2,3-dihydroxy-n-propyl)-2,4,6-triiodoisophthalamide (I) (2000g , 2.677mol) (produced by Zhejiang Stellite Pharmaceutical Co., Ltd.), sodium hydroxide (139.2g, 3.480mol) was dissolved in 50% ethylene glycol monomethyl ether aqueous solution, stirred at room temperature, added methyl iodide (380.1g, 2.677mol), TLC followed the reaction process, and the reaction was completed in 6h. Concentrate under reduced pressure and use resin to purify and separate. The specific method is: prepare 5 liters of macroporous adsorption resin regenerated with 40% methanol, pack it into a glass column with a diameter of 100mm, pour the product aqueous solution into it, and let it absorb statically. For more than two hours, gradient elution was carried out with different concentrations of methanol

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to view more

PUM

No PUM Login to view more

Abstract

The invention relates to a novel contrast medium for a triiodobenzene compound and also provides a preparation method of the compound. The triiodobenzene compound is 5-(N-methylacetamide)-N,N'-di(2.3-dyhydroxy n-propyl)-2,4,6-triiodo isophthalamide (I) and has a structural formula shown as the specification.

Description

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to view more

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to view more

Application Information

Patent Timeline
no application Login to view more
Owner ZHEJIANG STARRY PHARMA
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Try Eureka
PatSnap group products