Application of Picantron as Lymphatic Tracer
A tracer, the technology of Picantron, which is applied in the field of new drug indications, can solve the problems of residual preparation process at the injection site, slow tracer staining time, large diffusion of surrounding tissues, etc., and achieves low price, low toxicity, and high diffusion little effect
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Embodiment 1
[0041] Embodiment 1, the preparation of picantron hydrochloride
[0042] Weigh 1 g of picantron maleate as a starting material, dissolve it with MQ ultrapure water as a solvent, and ultrasonically dissolve it fully. Next, 717-strong base anion exchange resin (200mL swelling volume) was used as the exchanger for maleate radical exchange. Shake at room temperature for 30 minutes, take the solution out of the resin, soak the resin with water several times, and take out the free picantron solution as much as possible. Freeze-drying the obtained free picantron solution to obtain free picantron powder. Take MQ ultrapure water as a solvent to dissolve, take hydrochloric acid with a concentration equal to 1M to carry out a salt-forming reaction, and keep the reaction on a shaker for 1 hour. The reaction solution was freeze-dried to obtain picantron hydrochloride powder (yield 95%). 1 H-NMR (DMSO) δ-3.10 (dd, 4H), 3.82 (dd, 4H), 7.70 (d, 2H), 8.08 (d, 1H), 8.31 (s, 6H), 9.02 (d, 1H)...
Embodiment 2
[0043] Embodiment 2, the preparation of picantron sulfate
[0044] According to the method described in Example 1, replace "1M hydrochloric acid for salt-forming reaction" with "1M sulfuric acid for salt-forming reaction" to obtain Picantron sulfate powder. 1 H-NMR (DMSO) δ-3.10 (dd, 4H), 3.79 (dd, 4H), 7.65 (d, 2H), 7.92 (d, 1H), 8.16 (s, 6H), 9.03 (d, 1H), 9.49 (s, 1H), 10.96 (d, 2H).
Embodiment 3
[0045] Embodiment 3, the preparation of picantron trifluoroacetate
[0046] According to the method described in Example 1, replace "1M hydrochloric acid for salt formation reaction" with "1M trifluoroacetic acid for salt formation reaction" to obtain picantron trifluoroacetate powder. 1 H-NMR(DMSO)δ-3.10(dd, 4H), 3.80(dd, 4H), 7.64(d, 2H), 7.8.08(s, 6H, 1H), 9.01(d, 1H), 9.45(s , 1H), 10.97(d, 2H).
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