首页> 外国专利> PROCESS FOR PREPARING 2-HALO-NICERGOLINE DERIVATIVES AND THEIR ADDITION SALTS WITH ACIDS AND NEW 2-HALONICERGOLINES, COMPOSITIONS COMPRISING 2-HALONICERGOLINES AND PROCESS FOR PREPARING THE SAME

PROCESS FOR PREPARING 2-HALO-NICERGOLINE DERIVATIVES AND THEIR ADDITION SALTS WITH ACIDS AND NEW 2-HALONICERGOLINES, COMPOSITIONS COMPRISING 2-HALONICERGOLINES AND PROCESS FOR PREPARING THE SAME

机译:制备带有酸和新的2-卤代烯醇的2-卤代-麦角茶碱衍生物及其加成盐的方法,包含2-卤代烯醇的组合物及其制备方法

摘要

THE INVENTION CONCERNS A NEW PROCESS FOR THE PREPARATION OF PARTLY NEW 2-HALONICERGOLINE DERIVATIVES. /P P IT CONSISTS OF ESTERIFYING A 2-HALO-1-METHYL-LUMILYSERGOL OF FORMULA (II): BR/ (CF DRAWING IN BOPI) BR/ IN WHICH X REPRESENTS AN ATOM OF CHLORINE, BROMINE OR IODINE OR ITS ADDITIONAL SALT WITH AN ACID AND, POSSIBLY TO CONVERT THE DERIVATIVE OF 2-HALONICERGOLINE THUS OBTAINED INTO A SALT OF ADDITION WITH AN ACID. /P P THE COMPOUNDS OF THE INVENTION IMPROVES THE COGNITIVE FUNCTION OF THE BRAIN AND SHOWS ANTIHYPOXIC ACTION, A-ADRENERGIC BLOCKING ACTION AND AN ANTAGONISM ACTION WITH CALCIUM. / P P THE INVENTION ALSO CONCERNS PHARMACEUTICAL COMPOSITIONS CONTAINING A 2-HALONICERGOLINE.
机译:本发明考虑了用于制备部分新的2-卤代古兰经衍生物的新方法。

它由酯化式的2-卤代-1-甲基-鲁米色酚(II)组成:
(BOPI中的CF绘制)
X代表氯原子,溴或碘或其附加盐与酸的结合,并可能将2-卤代鹅油啉的衍生物转化为酸附加盐。

本发明的化合物改善了大脑的认知功能,并显示了钙的抗缺氧作用,α-肾上腺素阻断作用和拮抗作用。

本发明还考虑到包含2-卤代柠檬油的药物组合物。

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