A kind of medicine for preventing and treating acute kidney injury and its preparation method and application
A pharmaceutical and compound technology, applied in the field of oxazolopyrimidine compounds, can solve the problems of cell surface S1P1 reduction, lymphocyte reduction, etc., and achieve therapeutically applicable effects
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Embodiment 1
[0042] Example 1: 7-(1H-indole-7-carbonyl)oxazol[5,4-d]pyrimidin-2-yl 5-guanidinopyrimidine-2-carboxylate (Compound 1)
[0043]
[0044] In a three-necked flask equipped with a nitrogen protection device, a thermometer, and a reflux condenser, add 2.7g (0.015mol) of 5-guanidinopyrimidine-2-carboxylic acid and toluene (100ml) under nitrogen protection, and stir to make it dissolve. Then add 2.6g (0.016mol) of carbonyldiimidazole, heat to 80°C, and react for 2 hours, then add dropwise 2.2g (0.016mol) of oxazol[5,4-d]pyrimidin-2-ol in toluene (50ml) solution, and then heated to reflux, and reacted for 4 hours. After cooling the reaction solution, the solvent was evaporated under reduced pressure. The residue was washed with water and recrystallized with ethanol to obtain a white solid oxazol[5,4-d]pyrimidine-2- 3.9 g of 5-guanidinopyrimidine-2-carboxylate, yield 87%, ESI-MS: 301.07 [M+H] + .
[0045] Add aluminum trichloride (5.6g, 44.0mmol), toluene (100ml) into a three-nec...
Embodiment 2
[0049] Example 2: 7-(piperidine-4-carbonyl)oxazol[5,4-d]pyrimidin-2-yl 5-guanidinopyridine-2-carboxylate (Compound 2)
[0050]
[0051] According to the method of Example 1, replace 5-guanidinopyrimidine-2-carboxylic acid with 5-guanidinopyridine-2-carboxylic acid, and replace 1H-indole-7-acyl chloride with piperidine-4-acyl chloride to obtain a white solid , total yield 51%, ESI-MS: 411.15[M+H] + .
Embodiment 3
[0052] Example 3: 5-fluoro-7-(1H-pyrazole-5-carbonyl)oxazol[5,4-d]pyrimidin-2-yl 5-guanidinopyrimidine-2-carboxylate (Compound 3)
[0053]
[0054] According to the method of Example 1, replace oxazol[5,4-d]pyrimidin-2-ol with 5-fluoro-oxazol[5,4-d]pyrimidin-2-ol, and use 1H-pyrazole-5- Acid chloride replaced 1H-indole-7-acyl chloride to give a bright white solid with a total yield of 45%, ESI-MS: 413.08[M+H] + .
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