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MANUFACTURE OF VITAMIN B6

机译:维生素B6的生产

摘要

Formula I 3- unsubstituted, 3-substituted or 3,3-disubstituted 9-il Fig acyloxy-1,5-dihydro-8-methyl-pyrido of [3,4-e] [1,3] dioxepine and optionally, the method of manufacture is pyridoxine, solvent and formula II of the 4-methyl-5-alkoxy, under substantial absence of catalyst-oxazole of the formula III 2-unsubstituted, 2-monosubstituted or 2,2-disubstituted 4, 7-dihydro- (1, 3) - by the addition reaction dioxepine, a large amount of a suitable di (IV) Els-Alder adduct and a small amount of the appropriate 3-unsubstituted of formula V, 3-mono- or 3,3 -disubstituted 1,5-dihydro-8-methyl-pyrido produce a product mixture consisting of [3,4-e] [1,3] dioxepine-9 come into and essentially, unreacted from the product mixture by distillation under reduced pressure oxazole and dioxane substantially removed sepin starting material and then, (IV) adding a substantial anhydrous organic acid to the product mixture, while removing the all produced by distillation under reduced pressure to alkane in the presence of the substantially anhydrous organic acid Diels- Alder addition and by arranging the water re-produce the compound of formula V of the additional and, as a result, to produce the compounds of formula (I) in which more ah widening a carboxylic acid anhydride is added to the compound of formula V in the amount of a misfire by the purpose, optionally with this by achieving the deprotection and deacylation by acid hydrolysis of the acylated product of the formula I is manufactured it includes a switch Sikkim as pyridoxine. Pyridoxine is a well known form of vitamin B 6 The purpose is widely established.
机译:式I 3- [3,4-e] [1,3]二氧杂环丁烷的酰氧基-1,5-二氢-8-甲基-吡啶基,任选地,制造方法是吡ido醇,溶剂和4-甲基-5-烷氧基的式II,在基本上不存在式III的催化剂-恶唑的情况下,为2-未取代,2-单取代或2,2-二取代的4、7-二氢- (1,3)-通过二氧杂庚因的加成反应,大量合适的二(IV)Els-Alder加合物和少量合适的式V,3-单-或3,3-二取代的3-未取代1,5-二氢-8-甲基-吡啶基生成由[3,4-e] [1,3]二氧杂环庚烷-9组成的产物混合物,在减压下通过蒸馏将恶唑和二恶烷从产物混合物中基本上未反应基本上除去了Sepin起始原料,然后(IV)向产物混合物中加入了基本上无水的有机酸,同时除去了减压蒸馏生成的所有烷烃。存在基本无水的有机酸Diels-Alder加成反应,并通过安排水重制该加成化合物的式V化合物,结果制得其中羧酸盐进一步加宽的式(I)化合物出于目的,将酸酐以失火的量添加至式V的化合物中,任选地,通过将​​式I的酰化产物通过酸水解实现脱保护和脱酰,从而将其制备成包括辛基金作为吡ido醇的开关。吡rid醇是维生素B 6 的一种众所周知的形式。

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