Positron emission tomography radiotracer for diseases associated with translocator protein overexpression, translocator protein-targeting ligand for fluorescence imaging diagnosis and photodynamic therapy, and preparation method therefor
A technology of radiotracer and translocator protein, which is applied in photodynamic therapy, radioactive carriers, and radioactive preparations in vivo, to achieve the effects of shortening diagnosis time, improving emission, and high signal-to-noise ratio
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[0038] In order to achieve the stated purpose, the preparation method of the fluorine-18 labeled PET imaging radiotracer targeting translocation protein overexpression of the present invention may comprise the following steps: the preparation step of fluorine-18 reaction solution, dissolving the The fluorine-18 water generated by the cyclotron is added to acetonitrile (CH3CN, acetonitrile) together with the phase transfer catalyst and heated to a temperature of 85°C to 95°C to prepare the generated fluorine-18 reaction solution; the precursor preparation step, let 2-(4-Aryltrimethyltin-6,8-dichloroimidazo[1,2-a]pyridin-3-yl)dipropylacetamide and (diacetoxy)iodoarene derivatives Perform the reaction to prepare iodonium salt precursor (precursor A type) or let 2-(4-bromoaryl-6,8-dichloroimidazo[1,2-a]pyridin-3-yl)dipropylethyl Amide reacts with bis(pinacolate) diboron to prepare boron ester precursor (precursor Btype); iodonium salt reaction solution preparation step, the iodoni...
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[0059] Based on the principle that the inventor can properly define the concept of the relevant terms in order to explain his invention using the best method, it should be interpreted in accordance with the meaning and concept of the technical idea of the present invention.
[0060] The present invention will be described in detail below. However, the present invention can be realized in various forms without being limited by one embodiment disclosed below. The main purpose of this embodiment is to fully disclose the present invention and fully explain the scope of the present invention to those with ordinary knowledge.
[0061] figure 1 A chemical formula showing a synthesis process of a fluorine-18-labeled radiotracer using an iodonium precursor and a boroester precursor in an example of the present invention.
[0062] figure 2 A graph showing the HPLC chromatogram of the isolation of pure fluorine-18 labeled radiotracer from a synthetic mixture that is one example of a...
preparation example 1
[0133] Preparation 1: 2-(6,8-dichloro-2-(4-(trimethylstannyl)phenyl)-imidazo[1,2-a]pyridin-3-yl)-N, Preparation of N-dipropylacetamide
[0134]
[0135] (Step 1): Preparation of 4-(4-bromophenyl)-4-oxo-N,N-dipropylbutanamide
[0136] 3-(4-Bromobenzoyl)propionic acid (2.0g, 7.8mmol) and 1,1'-carbonyldiimidazole (1.4g, 8.6mmol) were dissolved in tetrahydrofuran (THF, 50ml) and stirred for 30 minutes. After 30 minutes, N,N'-dipropylamine (1.2 mL, 8.6 mmol) and triethylamine (1.3 ml, 9.4 mmol) were added and stirred for 3 hours. After the solvent was removed by negative pressure, the residue was extracted with ethyl acetate after being poured into 0.1N aqueous hydrogen chloride solution. The extracted organic solvent is treated with sodium sulfate and filtered, and the remaining organic solvent is evaporated by negative pressure. The residue was purified by column chromatography to obtain the target compound.
[0137] 1H NMR (400MHz, CDCl3) δ0.86(t, J=7.4Hz, 3H, CH3), 0.95(...
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