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首页> 外文期刊>Journal of Heterocyclic Chemistry: The International Journal of Heterocyclic Chemistry >A Convenient Synthesis of New Pyrazolo[4,3-d]pyrimidines and Their Fused Heterocycles
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A Convenient Synthesis of New Pyrazolo[4,3-d]pyrimidines and Their Fused Heterocycles

机译:新型吡唑并[4,3-d]嘧啶及其熔融杂环的简便合成

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摘要

A series of some fused heterocycles originated from pyrazolopyrimidines were synthesized using 4- amino1-methyl-3-propyl-1H-pyrazole-5-carboxamide as a starting material. The nucleophilic substitution reactions with different amino acids followed by cyclization and Suzuki-Miyaura cross-coupling reactions with different aryl boronic acids of 7-chloro-5-(4-chlorophenyl)-1-methyl-3-propyl-1H-pyrazolo[4,3-d] pyrimidine were performed. Also, the oxidative cyclization reactions of 1-(5-(4-chlorophenyl)-1- methyl-3-propyl-1H-pyrazolo[4,3-d]pyrimidin-7-yl)hydrazine with different aldehydes in the presence of diacetoxy iodobenzene are described. All the synthesized compounds were characterized by analytical and spectroscopic methods.
机译:以4-氨基1-甲基-3-丙基-1H-吡唑-5-羧酰胺为起始原料合成了一系列由吡唑并嘧啶衍生的稠合杂环。不同氨基酸的亲核取代反应,然后环化,Suzuki-Miyaura交叉偶联反应与7-氯-5-(4-氯苯基)-1-甲基-3-丙基-1H-吡唑并不同的芳基硼酸[4]进行了[3-3-d]嘧啶。另外,在存在下,1-(5-(4-氯苯基)-1-甲基-3-丙基-1H-吡唑并[4,3-d]嘧啶-7-基)肼与不同醛的氧化环化反应描述了二乙酰氧基碘苯。所有合成的化合物都通过分析和光谱方法表征。

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