embedded image or pharmaceutically acceptable derivatives and salts, racemates, isomers and/or tautomers thereof comprising cyclizing an azomethine ylide of general Formula:; embedded image wherein,A is a cyclic or non-cyclic group; Z is a carbon or a heteroatom; n is selected from 0, 1, 2 or 3; W, X and Y may be the same or different and each are selected from hydrogen; optionally substituted alkyl, alkenyl, alkynyl, amino, alkoxy, alkenoxy, alkynoxy, aryl, alkylthio, heterocyclyl; carboxy, carboxy ester, carboxamido, acyl, acyloxy, mercapto, halogen, nitro, sulfate, phosphate, cyano and optionally protected hydroxy; or W and X, together with the nitrogen and carbon atoms to which they are attached, form a saturated or unsaturated nitrogen containing heterocyclic group which may be optionally substituted or optionally fused to a saturated or unsaturated carbocyclic group, aryl group or heterocyclic group is provided."/> Preparation of fused polycyclic alkaloids by ring closure of azomethine ylides, novel compounds thereof and their use as chemotherapeutic agents
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Preparation of fused polycyclic alkaloids by ring closure of azomethine ylides, novel compounds thereof and their use as chemotherapeutic agents

机译:通过偶氮甲亚胺环的闭环制备稠合多环生物碱,其新型化合物及其作为化学治疗剂的用途

摘要

A method for the preparation of a compound of general Formula:; embedded image or pharmaceutically acceptable derivatives and salts, racemates, isomers and/or tautomers thereof comprising cyclizing an azomethine ylide of general Formula:; embedded image wherein,A is a cyclic or non-cyclic group; Z is a carbon or a heteroatom; n is selected from 0, 1, 2 or 3; W, X and Y may be the same or different and each are selected from hydrogen; optionally substituted alkyl, alkenyl, alkynyl, amino, alkoxy, alkenoxy, alkynoxy, aryl, alkylthio, heterocyclyl; carboxy, carboxy ester, carboxamido, acyl, acyloxy, mercapto, halogen, nitro, sulfate, phosphate, cyano and optionally protected hydroxy; or W and X, together with the nitrogen and carbon atoms to which they are attached, form a saturated or unsaturated nitrogen containing heterocyclic group which may be optionally substituted or optionally fused to a saturated or unsaturated carbocyclic group, aryl group or heterocyclic group is provided.
机译:通式化合物的制备方法: “嵌入式图像” 或其药学上可接受的衍生物和盐,外消旋体,异构体和/或互变异构体,包括环化以下通式的偶氮甲碱叶立德:; “嵌入式图像” 其中, A是循环或非循环基团; Z为碳或杂原子; n从0、1、2或3中选择; W,X和Y可以相同或不同,并且各自选自氢;任选取代的烷基,烯基,炔基,氨基,烷氧基,烯氧基,炔氧基,芳基,烷硫基,杂环基;羧基,羧基酯,羧酰胺基,酰基,酰氧基,巯基,卤素,硝基,硫酸根,磷酸根,氰基和任选保护的羟基;或W和X与它们所连接的氮和碳原子一起形成饱和或不饱和的含氮杂环基,其可以任选地被取代或任选地稠合到饱和或不饱和的碳环基,芳基或杂环基上。 。

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