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Synthesis of 6-aryl-4-aminopicolinates and 2-aryl-6-aminopyrimidine-4-carboxylates by direct suzuki coupling

机译:通过直接铃木偶联合成6-芳基-4-氨基吡啶啉酸酯和2-芳基-6-氨基嘧啶-4-羧酸酯

摘要

Improved methods of synthesizing 6-aryl-4-aminopicolinates, such as arylalkyl and alkyl 4-amino-3-chloro-6-(4-chloro-2-fluoro-3-methoxyphenyl)pyridine-2-carboxylates and arylalkyl and alkyl 4-amino-3-chloro-5-fluoro-6-(4-chloro-2-fluoro-3-methoxyphenyl)pyridine-2-carboxylates, are described herein. The improved methods include a direct Suzuki coupling step, which eliminates the protection/de-protection steps in the current chemical process, and therefore eliminates or reduces various raw materials, equipment and cycle time as well as modification of other process conditions including use of crude AP, use of ABA-diMe, and varying pH, catalyst concentration, solvent composition, and/or workup procedures. This includes synthesis of 2-aryl-6-aminopyrimidine-4-carboxylates.
机译:合成6-芳基-4-氨基吡啶甲酸酯,例如芳基烷基和烷基4-氨基-3-氯-6-(4-氯-2-氟-3-甲氧基苯基)吡啶-2-羧酸酯和芳基烷基和烷基4的改进方法本文描述了-氨基-3-氯-5-氟-6-(4-氯-2-氟-3-甲氧基苯基)吡啶-2-羧酸酯。改进的方法包括直接的Suzuki偶联步骤,该步骤取消了当前化学过程中的保护/去保护步骤,因此消除或减少了各种原材料,设备和循环时间,以及修改了其他工艺条件(包括使用原油) AP,使用ABA-diMe以及改变pH,催化剂浓度,溶剂组成和/或后处理程序。这包括2-芳基-6-氨基嘧啶-4-羧酸酯的合成。

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