首页> 外文期刊>Synthesis: International Journal of Methods in Synthetic Organic Chemistry >Efficient access to 2,7-diarylated pyrido[3,2- d]pyrimidines involving regioselective pallado-dehalogenation and suzuki cross-coupling reactions
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Efficient access to 2,7-diarylated pyrido[3,2- d]pyrimidines involving regioselective pallado-dehalogenation and suzuki cross-coupling reactions

机译:有效地获得涉及区域选择性帕拉多脱卤和铃木交叉偶联反应的2,7-二芳基吡啶并[3,2-d]嘧啶

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摘要

An efficient and original synthesis of various 2,7-disubstituted pyrido[3,2-d]pyrimidines is reported. The first synthesis of 2,7-dichloropyrido[3,2-d]pyrimidine, by selective palladium-catalyzed dechlorination of 2,4,7-trichloropyrido[3,2-d]pyrimidine at C-4, is described and its chemical reactivity is examined. Diarylated pyrido[3,2-d]pyrimidines were synthesized starting from 2,7-dichloropyrido[3,2-d]pyrimidine by regioselective Suzuki cross-coupling reaction at C-2 and then at C-7. ? Georg Thieme Verlag Stuttgart ?? New York.
机译:报道了各种2,7-二取代的吡啶并[3,2-d]嘧啶的有效和原始合成。描述了在C-4上通过钯催化的2,4,7-三氯吡啶并[3,2-d]嘧啶的选择性脱氯反应,首次合成了2,7-二氯吡啶并[3,2-d]嘧啶及其化学反应检查反应性。由2,7-二氯吡啶并[3,2-d]嘧啶开始的二芳基吡啶并[3,2-d]嘧啶的合成是通过在C-2,然后在C-7的区域选择性Suzuki交叉偶联反应进行的。 ? Georg Thieme Verlag斯图加特??纽约。

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