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Redox-induced pH-responsive methacrylate fluorine-containing monomer, synthesis method and application

A type of methacrylic acid and methacrylate technology, which is applied in the field of redox-induced pH-responsive methacrylate fluorine-containing monomers, can solve the problem of shortening, increase of fluorine signal peak width, and decrease of imaging signal-to-noise ratio and other problems, to achieve the effect of stable quality, simple synthesis method and high yield

Active Publication Date: 2020-04-21
INST OF BIOMEDICAL ENG CHINESE ACAD OF MEDICAL SCI
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Because the fluorine-containing organic ligands are directly grafted into the polymer or liposome molecular structure through chemical bonds, and then form nano-probes, which contributes to the improvement of material stability and toxicity, but due to the reduction of fluorine atoms degrees of freedom, so the T2 of the grafted material will be shortened, the peak width of the fluorine signal will increase, and the imaging signal-to-noise ratio will decrease

Method used

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  • Redox-induced pH-responsive methacrylate fluorine-containing monomer, synthesis method and application
  • Redox-induced pH-responsive methacrylate fluorine-containing monomer, synthesis method and application
  • Redox-induced pH-responsive methacrylate fluorine-containing monomer, synthesis method and application

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Experimental program
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Embodiment 1

[0025] The synthesis of embodiment 1 monomer M1

[0026] The chemical structure of monomer M1 is shown below. The specific synthesis steps are as follows: First, add 2-aminoethyl methacrylate hydrochloride (1.65 g, 10 mmol) and triethylamine (2.02 g, 20 mmol) in a 100 mL round bottom flask, add 50 mL of Tetrahydrofuran was dispersed and dissolved in water, and a tetrahydrofuran solution of 2,4-dinitrobenzenesulfonyl chloride (2.66 g, 10 mmol) was added dropwise under ice-bath conditions. After the addition was complete, the solution was returned to room temperature for 10 h. The reaction solution was distilled off the solvent under reduced pressure, and then separated by column chromatography, using ethyl acetate / petroleum ether mixture as the eluent, collecting the eluate containing the target compound, and after the solvent was evaporated, the intermediate product 2- ((2,4-Dinitrophenyl) sulfonamide) ethyl methacrylate, yield 85%. Next, add 2-((2,4-dinitrophenyl)sulfonamid...

Embodiment 2

[0030] Adjust the molar ratio of 3,3,3-trifluoropropan-1-ol to 2-((2,4-dinitrophenyl)sulfonamide)ethyl methacrylate to 2.5:1, and the others are the same as in the examples 1. The obtained product 2-((2,4-dinitro-N-(3,3,3-trifluoropropyl)phenyl)sulfonamide ethyl methacrylate has a yield of 90%.

Embodiment 3

[0032] The reaction temperature was adjusted to 40°C, and the others were the same as in Example 1. The resulting product 2-((2,4-dinitro-N-(3,3,3-trifluoropropyl)phenyl)sulfonamide methacrylic acid Ethyl ester, yield 91%.

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Abstract

The invention relates to a synthetic method and application of a redox induced pH-responsive type methacrylate fluorine-containing monomer. The general formula is shown in the specification, wherein a, b, c and d are respectively independent integers. The synthetic method comprises the following steps: with organic alkali as an acid-binding agent, enabling a methacrylate monomer containing a primary amine end group to react with 2,4-dinitrobenzene sulfonyl chloride in anhydrous tetrahydrofuran so as to obtain a sulfamide monomer; and with diethyl azodicarboxylate and triphenylphosphine as catalysts, enabling the sulfamide monomer to have a Mitsunobu reaction with a fluorine alcohol monomer, separating and purifying, and assembling in an aqueous solution. A strong electron withdrawing group2,4-dinitro-benzsulfamide exists in the structure disclosed by the invention and can rapidly have a nucleophilic substitution reaction with mercapto group so as to produce a secondary amine group, and the secondary amine group is protonized under corresponding pKa, so that redox induced pH response is realized. Development of fluorine-containing small molecules is facilitated, and the developmentneed of a 19FMRI probe is met. The synthetic method disclosed by the invention is simple, and the monomer is stable in quality and high in yield. The structural formula is as shown in the specification.

Description

technical field [0001] The invention relates to a redox-induced pH-responsive methacrylate fluorine-containing monomer, a synthesis method and an application. Background technique [0002] 19 F nucleus is a substance that is beneficial to nuclear magnetic resonance (NMR). Because it has almost no endogenous background interference in the body, it has been used in recent years 19 The related research of F elements in magnetic resonance imaging (MRI) has received more and more attention. Based on water molecules ( 1 H proton) nuclear magnetic resonance imaging, although it has high sensitivity, but due to the background signal interference of a large amount of water-containing substances in biological tissues, its imaging effect for specific positions is poor. In contrast, 19 F has almost no endogenous background interference in the organism, and only a very small amount of fluorine exists in human bones and teeth in solid form, so T2 very short, well below 19 Detection ...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): C07C311/17C07C303/38C07C303/40C07B59/00C08F283/06C08F220/38A61K51/06A61K49/12A61K101/02
CPCA61K49/126A61K51/06C07B59/001C07B2200/05C07C311/17C08F283/065C08F2438/03C08F220/387
Inventor 黄平升王伟伟秦怡博孔德领
Owner INST OF BIOMEDICAL ENG CHINESE ACAD OF MEDICAL SCI
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