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Synthesis of 2-alkylcysteine via phase transfer catalysis

机译:相转移催化合成2-烷基半胱氨酸

摘要

Non-natural amino acids such as 2-alkylated amino acids allow for the synthesis of a wider variety of peptidal and non-peptidal pharmaceutically active agents. In one embodiment, the present invention provides methods of preparing 2-alkylcysteine derivatives. In another embodiment, the method comprises forming a 2-alkylcysteine derivative from a cysteine derivative in the presence of a phase transfer catalyst. In particular, the present invention provides methods for preparing 2-methylcysteine derivatives.;The present invention also discloses a method of preparing a class of iron chelating agents related to desferrithiocin, all of which contain a thiazoline ring. In one aspect, an aryl nitrile or imidate is condensed with cysteine or a 2-alkyl cysteine. The present invention also relates to the preparation of 4,5-dihydro-2-(2,4-dihydroxyphenyl)-4-alkyl-thiazole-4-carboxylic acids, such as 4,5-dihydro-2-(2,4-dihydroxyphenyl)-4-methyl-thiazole-4-carboxylic acid.
机译:非天然氨基酸,例如2-烷基化氨基酸允许合成更多种肽和非肽药物活性剂。在一个实施方案中,本发明提供了制备2-烷基半胱氨酸衍生物的方法。在另一个实施方案中,该方法包括在相转移催化剂的存在下由半胱氨酸衍生物形成2-烷基半胱氨酸衍生物。特别地,本发明提供了制备2-甲基半胱氨酸衍生物的方法。本发明还公开了一种制备与去铁硫属素有关的铁螯合剂的方法,所述铁螯合剂均含有噻唑啉环。一方面,芳基腈或亚氨酸酯与半胱氨酸或2-烷基半胱氨酸缩合。本发明还涉及4,5-二氢-2-(2,4-二羟基苯基)-4-烷基噻唑-4-羧酸,例如4,5-二氢-2-(2,4)的制备。 (-二羟基苯基)-4-甲基-噻唑-4-羧酸。

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