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MOLECULAR DIVERSITY TECHNOLOGY OF THIAZOLE LIBRARY BASED ON COMBINATORIAL CHEMISTRY

机译:基于组合化学的噻唑文库分子多样性技术

摘要

Molecular diversity technology using a combinatorial chemical method of a thiazole derivate is provided to easily test biological activation of a disease target by quickly producing a target compound with high purity by using a solution phase reaction. In a method for producing a thiazole derivate represented by formula(1) generated by combinatorially and chemically reacting compounds of a formula(A) or a formula(B) with compounds of a formula(C), R^a in the formula(1) is selected from a group comprising alkyl, cycloalkyl, heterocyclic which is not substituted or substituted for phenyl substituted as alkyl, alkenyl, alkynyl, alkoxy, and halogen of C1-C10. R^b is aliphatic and aromatic hydrocarbon derivate compounds of C5-C10 which are not substituted or substituted for C1 and alkoxy and includes straight or side chain alkyl, phenoxymethyl, substituted phenoxymethyl, aniline, C6H4NHCOR2(Anilide), and pyridine of C1-C8. R^c consists of hydrogen atom, CN(Cyano Group), C1, COOH(Carboxyl Group), methoxy, ethoxy, and CONHR3N(Amide). X contains sulfur atom, SO2(Sulfur Dioxide), NH, piperazine, and single-bond morpholine. R2 is phenyl or phenylmethyl substituted for alkyl or alkoxy. R3 is aliphatic and aromatic hydrocarbon derivate compounds of C5-C10 which are substituted or not substituted.
机译:提供了使用噻唑衍生物的组合化学方法的分子多样性技术,以通过使用溶液相反应快速生产高纯度的目标化合物来容易地测试疾病目标的生物活化。在通过式(A)或式(B)的化合物与式(C)的化合物的组合和化学反应产生的式(1)表示的噻唑衍生物的制备方法中,式(1)中的R a )选自烷基,环烷基,未被取代或取代被取代为C1-C10的烷基,烯基,炔基,烷氧基和卤素的苯基的基团。 R b是不被C 1和烷氧基取代或取代的C 5 -C 10的脂族和芳族烃衍生物,包括直链或侧链的烷基,苯氧基甲基,取代的苯氧基甲基,苯胺,C 6 H 4 NHCOR 2(苯胺)和C 1 -C 8的吡啶。 R c由氢原子,CN(氰基),Cl,COOH(羧基),甲氧基,乙氧基和CONHR 3 N(酰胺)组成。 X包含硫原子,SO2(二氧化硫),NH,哌嗪和单键吗啉。 R 2是被烷基或烷氧基取代的苯基或苯甲基。 R 3是被取代或未被取代的C 5 -C 10的脂族和芳族烃衍生物。

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