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AMIDES, METHODS OF THEIR SYNTHESIS AND PHARMACEUTICAL COMPOSITION SHOWING PROPERTY OF CHANNEL OPENING FOR CELLULAR POTASSIUM

机译:纤维素钾通道的酰胺,合成方法和药物组合物的显示性能

摘要

FIELD: organic chemistry. SUBSTANCE: product: amides of the formula (I): where: a): E - nitrogen and X - phenylsulfonyl; b): E - group CZ where C - ring carbon atom; Z - hydrogen, cyano-group, halogen, hydroxyl, alkyl or alkoxyl; X - phenylcarbonyl, phenylsulfinyl or phenyl sulfonyl; c): X - cyano-group and Z - phenylsulfonyl; R2 and R3 free alkyl or alkyl substituted with fluorine or they together form 3-5-membered cycloalkyl, and pharmcomposition based on amides of the formula (I) and methods of amide synthesis. Method 1. Reagent 1: the corresponding aniline. Reagent 2: the corresponding acid. Method 2. Reagent 1: amide of the formula (I) containing hydroxyl-protected group. Reaction condition: protective group removing. Method 3. Reagent 1: amide of the formula (I) where X - phenyl sulfide. Reagent 2: oxidizing agent. Synthesized compounds can be used in medicine. EFFECT: improved method of synthesis. 6 cl, 2 tbl
机译:领域:有机化学。物质:产品:式(I)的酰胺:其中:a):E-氮和X-苯磺酰基; b):E-CZ基团,其中C-环碳原子; Z-氢,氰基,卤素,羟基,烷基或烷氧基; X-苯基羰基,苯基亚磺酰基或苯基磺酰基; c):X-氰基和Z-苯磺酰基; R 2 和R 3 游离烷基或被氟取代的烷基或它们一起形成3-5元环烷基,并基于式(I)的酰胺进行药物合成和方法酰胺的合成。方法1.试剂1:相应的苯胺。试剂2:相应的酸。方法2.试剂1:含有羟基保护基的式(I)的酰胺。反应条件:保护基去除。方法3。试剂1:式(I)的酰胺,其中X-苯硫醚。试剂2:氧化剂。合成的化合物可用于医学。效果:改进的合成方法。 6厘升,2汤匙

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