Process for the preparation of (hetero)arylalk(en/in)ylamines and
(hetero)arylalkinylamines
    61.
    发明授权
    Process for the preparation of (hetero)arylalk(en/in)ylamines and (hetero)arylalkinylamines 失效
    (杂)芳基(en / in)基胺和(杂)芳基烯基胺的制备方法

    公开(公告)号:US5283363A

    公开(公告)日:1994-02-01

    申请号:US821202

    申请日:1992-01-16

    摘要: The invention relates to a new process for the preparation of (hetero)arylalk(en/in)ylamines of the formula (I) ##STR1## in which A represents ethane-1,2-diyl (ethylene, dimethylene, --CH.sub.2 --CH.sub.2 --) or represents ethene-1,2-diyl (ethenylene, vinylene, --CH.dbd.CH--) or represents ethine-1,2-diyl (ethinylene, --C.ident.C--),characterized in that(a) in the event that, in formula (I), A represents ethine-1,2-diyl, halogeno(hetero)aryl compounds of the general formula (II)Ar--X (II)are reacted with aminoalkinyl compounds of the general formula (III) ##STR2## and, if appropriate, (b) in the event that, in formula (I), A represents ethane-1,2-diyl or ethene-1,2-diyl, the new (hetero)aralkinylamines which are obtained by the process step described under (a), of the general formula (Ia), ##STR3## are reacted with a hydrogenating agent, if appropriate in the presence of a catalyst and if appropriate in the presence of a diluent, the definitions applying to Ar, R.sup.1, R.sup.2 and X being those mentioned in the description, and their use as intermediates for medicoments and plant protection agents, in this case in particular herbicides.

    摘要翻译: 本发明涉及一种制备式(I)(*化学结构*)(I)的(杂)芳基烯(烯/茚)基胺的新方法,其中A代表乙烷-1,2-二基(乙烯, 二亚乙基,-CH 2 -CH 2 - )或代表乙烯-1,2-二基(亚乙烯基,亚乙烯基,-CH = CH-)或代表乙炔-1,2-二基(亚乙烯基,-C + 5 C-),其特征在于 (a)在式(I)中A表示乙炔-1,2-二基的情况下,通式(Ⅱ)Ar-X(Ⅱ)的卤代(杂)芳基化合物与 通式(III)(*化学结构*)(III),如果合适,(b)在式(I)中,A表示乙烷-1,2-二基或乙烯-1,2-二基 通过通式(Ia)中描述的方法步骤(Ia),(*化学结构*)(Ia)获得的新的(杂)芳炔基胺与氢化剂反应,如果合适,在存在下 的催化剂,如果在稀释剂存在下适当,定义a 适用于Ar,R1,R2和X是说明书中提及的那些,它们用作药物和植物保护剂的中间体,在这种情况下特别是除草剂。

    Antimycotic agents
    65.
    发明授权
    Antimycotic agents 失效
    抗真菌剂

    公开(公告)号:US4925865A

    公开(公告)日:1990-05-15

    申请号:US246729

    申请日:1988-09-20

    摘要: Combating mycoses in humans and other animals with hydroxyalkyl-azolyl derivatives of the formula ##STR1## in which R stands for hydrogen, alkyl or acyl,R.sup.1 stands for halogen, optionally substituted phenyl or the --Z--R.sup.3 grouping,R.sup.2 stands for optionally substituted alkyl, optionally substituted cycloalkyl, optionally substituted naphthyl, for the radical of the formula ##STR2## or for the radical of the formula ##STR3## X stands for nitrogen or a CH group and Y stands for the --CH.sub.2 --CH.sub.2 --, --CH.dbd.CH--, --C.tbd.C--, ##STR4## groupings, whereinR.sup.5, R.sup.6, R.sup.7 and R.sup.8 independently of one another stand for hydrogen or alkyl having 1 to 4 carbon atoms,and their acid addition salts.

    摘要翻译: 在人类和其他动物中与下列化合物的羟基烷基 - 唑基衍生物(I)抗真菌病,其中R代表氢,烷基或酰基,R1代表卤素,任选取代的苯基或-Z-R3基,R2代表 对于任选取代的烷基,任选取代的环烷基,任选取代的萘基,对于式的基团或对于式的基团,X代表氮或CH基团,Y代表-CH 2 -CH 2 - ,其中R5,R6,R7和R8彼此独立地代表氢或具有1-4个碳原子的烷基,以及它们的酸加成盐。