2-methyl-5-nitro glyoxaline compound, preparation and use thereof
A technology of nitroimidazoles and nitroimidazoles, applied in the application field of nitroimidazole complexes and their precursors in tumor imaging agents, to achieve high tumor uptake
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Embodiment 1
[0033] Compound MNIEC provided by the invention is synthesized according to the synthetic route shown below:
[0034]
[0035] The reagents used in each step are:
[0036] (a) EtOTFA, Et 3 N and MeOH;
[0037] (b) 2-bromoethanol, K 2 CO 3 and CH 3 CN;
[0038] (c)CH 3 SO 2 Cl, CH 2 Cl 2 and Et 3 N;
[0039] (d) Compound 1, K 2 CO 3 and CH 3 CN;
[0040] (e) NaOH and MeOH
[0041] Specific steps are as follows:
[0042] Synthesis of Tri-TFA cyclam (compound 1):
[0043] In a dry 50mL three-necked flask, cyclam (1.0g, 5mmol) and triethylamine (0.69mL, 5mmol) were dissolved in 20mL of anhydrous methanol, nitrogen protection was introduced and the reaction solution was kept at 0-5 with an ice-water bath. ℃, then added ethyl trifluoroacetate (6.0mL, 50.0mmol) dropwise, continued the dropwise addition for ten minutes, stirred and reacted for 7 hours, suspended and evaporated to remove the solvent, the residue was passed through a small silica gel column, and eth...
Embodiment 2
[0052] preparation 99m TcO-MNIEC complex
[0053] 1) 99m Preparation of TcO-GH
[0054] Weigh 25 mg of GH ligand, dissolve it completely with 0.5 mL of normal saline, add 0.5 mL of SnCl 2 2H 2 O (1mg / mL, 0.1M HCI), adjust pH=7-7.5, add 0.5mL of freshly rinsed 99m TCO 4 - The solution (approximately 10 mCi) was heated in a water bath at 40° C. for 10 minutes, then cooled to room temperature, and prepared as a precursor for the ligand exchange method.
[0055] 2) 99m Preparation of TcO-MNIEC
[0056] Dissolve 20 mg of the compound MNIEC ligand in 20 mL of methanol, take out 0.15 mL and put it into a penicillin vial, adjust the pH value to 13 with 1.0 mL of pH=13, that is, 0.1 M NaOH buffer solution, and add 0.15 mL of 99m Tc-GH solution, the mixture was heated in a boiling water bath for 45 minutes, and filtered through a filter membrane to obtain an electrically neutral and water-soluble target complex, and the labeling rate was greater than 95%.
Embodiment 3
[0058] preparation 99m TcN-MNIEC complex
[0059] (1) Intermediate [ 99m TcN] 2+ preparation of
[0060] Can be prepared in two ways 99m TcN intermediates, namely
[0061] Take 1~2mL 99m TCO 4 - Add the fresh eluent to the DTCZ kit, shake well, and heat in a boiling water bath for 15 minutes to obtain the intermediate [ 99m TcN] 2+ , the marking rate is greater than 98%;
[0062] or
[0063] Take 1~2mL 99m TCO 4 - Add the fresh eluent into the SDH kit, shake well, and let it stand at room temperature for 15 minutes to obtain the intermediate [ 99m TcN] 2+ , The labeling rate is above 98%.
[0064] (2) 99m Preparation of TcN-MNIEC
[0065] Take 0.1mL of the ligand solution MNIEC prepared above and put it into a penicillin vial, adjust the pH value of the MNIEC ligand solution to 13 with 1.0mL of 0.1M NaOH buffer solution, and then add 0.1mL[ 99m TcN] 2+ For the intermediate, heat in a boiling water bath for 40 minutes to obtain an electrically neutral and wate...
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