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Structural revision in pyrazole Chemistry

机译:吡唑化学的结构修订

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摘要

Reaction of several heteroarylhydrazines withbeta-diketones has been incorrectly reported togeneratetriazepines or diazepines.It has now been firmly established that these reactions lead to the formation of pyrazoles.Further,many workers have reported the formation of pyrazoles in the reaction of heteroarylhydrzaines with trifluoromethyl 1,3-diketones,whereas the actual products were found to be 5-hydroxy-5-trifluoromethyl-4,5-dihydro-1H-pyrazoles.Itwasalso establshed that iwth a trifluoromethyl beta-diketone and hydrazines,the location of the CF_3 group at position 3 or 5 pyrazoles depends on the nature of the hydrazine.Erroneous reports concening the structure of the products obtained by the reaciton of dehydroacetic acid withhydrazines have also been revised.
机译:已错误地报道了几种杂芳基肼与β-二酮的反应生成三氮杂or或二氮杂..现已确定这些反应会导致吡唑的形成。此外,许多工作人员报道了杂芳基肼基嗪与三氟甲基1的反应中吡唑的形成。 3-二酮,而实际的产物是5-羟基-5-三氟甲基-4,5-二氢-1H-吡唑。还确定了三氟甲基β-二酮和肼,CF_3的位置在3或5吡唑取决于肼的性质。错误的报告也证实了通过脱氢乙酸与肼反应形成的产物结构的错误报道。

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