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A New, Simple, and General Synthesis of N-Oxides of Iodopyridines and Iodoquinolines via the Diazotization–Iodination of Heterocyclic Amino N-Oxides in the Presence of p-Toluenesulfonic Acid in Water
Synthesis ( IF 2.2 ) Pub Date : 2017-12-13 , DOI: 10.1055/s-0036-1591738
Elena Krasnokutskaya , Alexey Chudinov , Victor Filimonov

Abstract

The diazotization of a series of N-oxides of aminopyridines and aminoquinolines under the action of sodium nitrite in the presence of KI and p-TsOH in water at room temperature leads to the formation of the corresponding N-oxides of iodopyridines and iodoquinolines in high yields. The method has a general character and can be used for the preparation of 3-, 2-, and 4- N-oxides of iodopyridines.

The diazotization of a series of N-oxides of aminopyridines and aminoquinolines under the action of sodium nitrite in the presence of KI and p-TsOH in water at room temperature leads to the formation of the corresponding N-oxides of iodopyridines and iodoquinolines in high yields. The method has a general character and can be used for the preparation of 3-, 2-, and 4- N-oxides of iodopyridines.



中文翻译:

在水中对甲苯磺酸存在下,通过杂环氨基N-氧化物的重氮化-碘化反应,可以合成碘,吡啶和碘代喹啉的N-氧化物

摘要

在室温下水中,在KI和p -TsOH存在下,在亚硝酸钠的作用下,亚硝酸钠作用下,一系列氨基吡啶和氨基喹啉的N-氧化物重氮化导致碘代吡啶和碘喹啉的相应N-氧化物的高收率形成。 。该方法具有一般性,可用于制备碘吡啶的3-,2-和4- N-氧化物。

在室温下水中,在KI和p -TsOH存在下,在亚硝酸钠的作用下,亚硝酸钠作用下,一系列氨基吡啶和氨基喹啉的N-氧化物重氮化导致碘代吡啶和碘喹啉的相应N-氧化物的高收率形成。 。该方法具有一般性,可用于制备碘吡啶的3-,2-和4- N-氧化物。

更新日期:2017-12-13
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