首页> 外国专利> 3,4,5 - -Trimethoxyphenyl - (3,4 - dimethyl - 2 - pyridyl) - carbinol, and 1,3,4 - trimethylsulphonium - 2 - (3,4,5 - trim ethoxy benzyl) - 1, 2,5,6 - tetrahydropyrin and method for their preparation

3,4,5 - -Trimethoxyphenyl - (3,4 - dimethyl - 2 - pyridyl) - carbinol, and 1,3,4 - trimethylsulphonium - 2 - (3,4,5 - trim ethoxy benzyl) - 1, 2,5,6 - tetrahydropyrin and method for their preparation

机译:3,4,5--三甲氧基苯基-(3,4--二甲基-2-吡啶基)-甲醇和1,3,4-三甲基--2-(3,4,5-三乙氧基苄基)-1,2, 5,6-四氢吡喃及其制备方法

摘要

A process for the preparation of 1,3,4-trimethyl-2-(3,4,5-trimethoxybenzyl) 1,2,5,6-tetrahydropyridine of formula (I) and its addition salts with pharmaceutically acceptable acids, for example halohydrides, which comprises in a first stage reacting 3,4,5-trimethoxybenzaldehyde of formula with 2-bromo-3,4-dimethylpyridine of formula the said reaction being effected in an inert solvent in the presence of butyl-lithium at a reaction temperature between-40.degree.C and ambient temperature, to form as an intermediate product 3,4,5-trimethoxyphenyl-(3,4-dimethyl-2-pyridyl) carbinol of formula (II) which in a second stage is reacted at a temperature below 20.degree.C with thionyl chloride, the chloride thus obtained is dissolved in glacial acetic acid and reduced with powdered zinc to form a product which is treated with methyl iodide to produce 1,3,4-trimethyl-2-(3,4,5-trimethoxybenzyl)-pyridine iodide, which is treated with sodium borohydride to produce the compound of formula I which, if desire, is converted into an acid addition salts thereof with a pharmaceutically acceptable acid, for example a halohydride.
机译:制备式(I)的1,3,4-三甲基-2-(3,4,5-三甲氧基苄基)1,2,5,6-四氢吡啶及其与药学上可接受的酸的加成盐的方法卤化物,其包括在第一步中使式的3,4,5-三甲氧基苯甲醛与式的2-溴-3,4-二甲基吡啶反应,所述反应在惰性溶剂中在丁基锂存在下于反应温度下进行在-40℃至环境温度之间,形成式(II)的3,4,5-三甲氧基苯基-(3,4-二甲基-2-吡啶基)甲醇的中间体产物,该醇在第二阶段中与用亚硫酰氯在低于20℃的温度下,将得到的氯化物溶于冰乙酸中,并用锌粉还原,形成产物,用碘代甲烷处理,得到1,3,4-三甲基-2-( 3,4,5-三甲氧基苄基)-吡啶碘化物,用硼氢化钠处理,得到式I化合物,如果将其与药学上可接受的酸,例如卤化氢,转化为其酸加成盐。

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