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首页> 外文期刊>The Journal of Organic Chemistry >Application of Pd-Catalyzed Cross-Coupling Reactions in the Synthesis of 5,5-Dimethy1-5,6-dihydro-4H-pyrrolo[1,2-b]pyrazoles that Inhibit ALK5 Kinase
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Application of Pd-Catalyzed Cross-Coupling Reactions in the Synthesis of 5,5-Dimethy1-5,6-dihydro-4H-pyrrolo[1,2-b]pyrazoles that Inhibit ALK5 Kinase

机译:钯催化的交叉偶联反应在抑制ALK5激酶的5,5-二甲基1-5,6-二氢-4H-吡咯并[1,2-b]吡唑的合成中的应用

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摘要

C-H activation of position 3 of a substituted pyrazole ring catalyzed by palladium(II) was straightforward and convenient for arylated or heteroarylated 5,5-dimethyl-5,6dihydro-4H-pyrrolo[1,2-b]pyrazoles. Moreover, we introduced simple protection of the nitrogen in the pyridin-2-yl directing group, which otherwise does not allow a cross-coupling reaction, by transformation to the N-oxide. Selected final products were reasonably selective ALK5 kinase inhibitors.
机译:钯(II)催化的取代吡唑环位置3的C-H活化对于芳基化或杂芳基化的5,5-二甲基-5,6二氢-4H-吡咯并[1,2-b]吡唑是直接且方便的。此外,我们引入了对吡啶-2-基导向基团中氮的简单保护,否则该氮原子不允许通过转化为N-氧化物进行交叉偶联反应。选定的最终产品是合理选择的ALK5激酶抑制剂。

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