在48%的氢溴酸水溶液中已经实现了将1-氨基吡唑和1-烷基氨基吡唑重排成相应的5-氨基吡唑。通过开环-开环机理发生的反应,构成了制备1-取代的5-氨基吡唑的新方法。产品已根据1 H和13 C nmr光谱结果以及与真实样品的比较进行了鉴定。
DOI:
10.1039/p19900000809
作为产物:
描述:
1H-吡唑-1-胺 、 alkaline earth salt of/the/ methylsulfuric acid 以71%的产率得到N-(pyrazol-1-yl)formamide
参考文献:
名称:
Rearrangement of N-(alkylamino)azoles in acid media: a new entry to C-amino-N-substituted azoles
摘要:
A ring-opening/ring-closure mechanism for the thermal rearrangement of 1-(alkylamino)pyrazoles into 5-amino-1-alkylpyrazoles in acid medium has been established. 1-(Benzylamino)pyrazoles show a different reactivity, affording bis(5-amino-1-benzyl-4-pyrazolyl)phenylmethanes. The reaction was extended to 1-(alkylamino)indazoles but failed in the case of 1-(alkylamino)-1,2,4-triazoles.