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Derivatives of 3 - amino - 4 - phenyl - 5,6 dihydro - 2H - (1,4) oxazine

机译:3-氨基-4-苯基-5,6二氢-2H-(1,4)恶嗪的衍生物

摘要

They have the activity of inhibiting bacteria and / or bacteria, their reproduction, drug synthesis containing these substances, and their use as therapeutic active substances. The active compound of the invention can be used for treatment and / or prevention, such as Alzheimer's disease and type 2 diabetes. Item 1: a formula compound (1)wherein X is O or S, R1 is selected from the group consisting of i) lower alkyl, ii) lower alkyl substituted by 1-5 substituents individually selected from cycloalkyl, halogen, halogen-lower alkoxy and lower alkoxy and iii) cycloalkyl , R2 is selected from the group consisting of i) H, ii) lower alkyl, iii) lower alkyl substituted by 1-5 substituents individually selected from cycloalkyl, halogen, halogen-lower alkoxy, heterocyclyl and lower alkoxy, iv) aryl, v ) aryl substituted by 1-4 substituents individually selected from cyano, cyano-lower alkyl, halogen, halogen-lower alkoxy, halogen-lower alkyl, heteroaryl, lower alkoxy,(lower alkoxy)-lower alkyl and lower alkyl, vi) cycloalkyl, vii) cycloalkyl substituted by 1-4 substituents individually selected from cyano, cyano-lower alkyl, halogen, halogen-lower alkoxy, halogen-lower alkyl, lower alkoxy, ( lower alkoxy)-lower alkyl and lower alkyl, viii) heteroaryl, ix) heteroaryl substituted by 1-4 substituents individually selected from aryl, cyano, cyano-lower alkyl, halogen, halogen-lower alkoxy, halogen-lower alkyl, cycloalkyl-alkoxy lower, (lower alkenyl) -alkoxy lower, aryl-lower alkoxy, heteroaryl, heterocyclyl, lower alkoxy,1.1.1.1 (low oxygen) - non cyclohexane was replaced by 1-4 substitutes, including: aminobenzene, cyanogen, cyano-below, halogenated, halo-below, halo-below, low oxygen (low oxygen), alcox (low oxygen) - low layer and tar, R3 is elected in the group consisting of (I) hydrogen halide and (II) lower tar, R4 is elected in the group consisting of (I) H and (II) lower tar, R5 is elected in the group consisting of (I) H and (II) lower tar, R6 is elected in the group consisting of (I) H and (II) lower tar.R7 was selected from a group consisting of (I) h, (II) arilo and (III) lower tar and (n) 0, 1 or 2 or salts acceptable to the drug.
机译:它们具有抑制细菌和/或细菌的活性,它们的繁殖,包含这些物质的药物合成以及它们作为治疗活性物质的用途。本发明的活性化合物可以用于治疗和/或预防,例如阿尔茨海默氏病和2型糖尿病。第1项:式(1),其中X为O或S,R 1选自:i)低级烷基,ii)被1-5个取代基取代的低级烷基,所述取代基分别选自环烷基,卤素,卤素-低级烷氧基和低级烷氧基和iii)环烷基,R2选自i)H,ii)低级烷基,iii)被1-5个取代基取代的低级烷基,它们分别选自环烷基,卤素,卤素-低级烷氧基,杂环基和低级烷氧基,iv)芳基,v)被1-4个取代基取代的芳基,所述取代基分别选自氰基,氰基-低级烷基,卤素,卤素-低级烷氧基,卤素-低级烷基,杂芳基,低级烷氧基,(低级烷氧基)-低级烷基和低级烷基,vi)环烷基,vii)被1-4个取代基取代的环烷基,所述取代基分别选自氰基,氰基-低级烷基,卤素,卤素-低级烷氧基,卤素-低级烷基,低级烷氧基,(低级烷氧基)-低级烷基和低级烷基,viii)杂芳基,ix)被1-4个取代基取代的杂芳基各自选自芳基,氰基,氰基-低级烷基,卤素,卤素-低级烷氧基,卤素-低级烷基,环烷基-烷氧基低级,(低级烯基)-烷氧基低级,芳基-低级烷氧基,杂芳基,杂环基,低级烷氧基, 1.1.1.1(低氧)-非环己烷已被1-4个替代物取代,包括:氨基苯,氰,氰基以下,卤代,卤代以下,卤代以下,低氧(低氧),醇(低氧) -低层和焦油,R3在(I)卤化氢和(II)低焦油组成的组中选择,R4在(I)H和(II)低焦油组成的组中选择,R5在(I)H和(II)下焦油组成的组,R6在(I)H和(II)下焦油组成的组中选择.R7选自(I)h,(II)芳基(III)下焦油和(n)0、1或2或药物可接受的盐。

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