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TETRAZOLE DERIVATIVES, METHOD OF THEIR SYNTHESIS AND PHARMACEUTICAL COMPOSITION SHOWING PROPERTY OF ANTAGONIST OF ANGIOTENSIN-II RECEPTORS
TETRAZOLE DERIVATIVES, METHOD OF THEIR SYNTHESIS AND PHARMACEUTICAL COMPOSITION SHOWING PROPERTY OF ANTAGONIST OF ANGIOTENSIN-II RECEPTORS
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机译:四唑衍生物,其合成方法和血管紧张素II受体拮抗剂的药理显示性能
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FIELD: organic chemistry. SUBSTANCE: product: 5-[4'-[2-butyl-4-chloro-5-(3-methyl-1,2,4-oxaziazole-5-yl) -1-imidazolylmethylbiphenyl-2-yl] ]-triphenylmethyl-1H-tetrazole, empirical formula is C43H37N8ClO, yield is 43%, m. p. is 175-177 C. Analysis: thin-layer chromatography in solvent toluene:ethyl acetate, 10:1; value Rf = 0.4. Synthesized compounds were used in medicine for hypertension and cardiac-vascular diseases treatment. EFFECT: improved method of synthesis. 7 cl, 3 dwg
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机译:领域:有机化学。物质:产物:5- [4'-[2-丁基-4-氯-5-(3-甲基-1,2,4-恶二唑-5-基)-1-咪唑基甲基联苯-2-基]]-三苯甲基-1H-四唑,经验公式为C 43 Sub> H 37 Sub> N 8 Sub> ClO,收率为43%,m。 p。分析:在175-177℃下进行薄层色谱。值R f Sub> = 0.4。合成的化合物被用于治疗高血压和心血管疾病的药物。效果:改进的合成方法。 7厘升,3公升
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