Triazole antifungal agents
    1.
    发明公开
    Triazole antifungal agents 失效
    抗炎三唑。

    公开(公告)号:EP0104734A1

    公开(公告)日:1984-04-04

    申请号:EP83304614.7

    申请日:1983-08-10

    摘要: Triazole antifungal agents of the formula:-
    and their O-esters and O-ethers, where R is a phenyl group optionally substituted by 1 to 3 substituents each independently selected from F, Cl, Br, 1, trifluoromethyl, C 1 -C 4 alkyl and C 1 -C 4 alkoxy, or R is a 5-chloro-pyrid-2-yl group; and n is zero or an integer of from 1 to 5; and their pharmaceutically and agriculturally acceptable salts.
    The compounds are useful as human and agricultural fungicides.

    摘要翻译: 三唑抗真菌剂,其结构如下: - ... ...及其O-酯和O-醚,其中R是任选被1至3个独立地选自F,Cl,Br,I,三氟甲基的取代基取代的苯基 ,C 1 -C 4烷基和C 1 -C 4烷氧基,或R是5-氯 - 吡啶-2-基; ...和n为0或1至5的整数;以及它们的药学上和农业上可接受的盐。 该化合物可用作人和农业杀真菌剂。

    Triazole antifungal agents
    3.
    发明公开
    Triazole antifungal agents 失效
    三唑类抗真菌剂

    公开(公告)号:EP0136063A3

    公开(公告)日:1985-12-18

    申请号:EP84305708

    申请日:1984-08-22

    摘要: Triazole antifungal agents of the formula:
    and their salts,
    where n is 0 or an integer of from 1 to 4, and X is selected from (a) optionally substituted phenoxy (b) optionally substituted heteroaryl-oxy (c) -S(O) m ·(C 1 -C 4 alkyl) where m is 0, 1 or 2 and (d) -CONR 3 R 4 where R 3 and R 4 are either H or C 1 -C 4 alkyl or together with the nitrogen atom to which they are attached form a pyrrolidinyl, piperidino, morpholino or optionally substituted piperazinyl group. The compounds are useful as human and plant antifungal agents.

    摘要翻译: 下式的三唑抗真菌剂及其盐,其中n为0或1至4的整数,并且X选自(a)任选取代的苯氧基(b)任选取代的杂芳基 - 氧基(c)-S(O) )m·(C 1 -C 4烷基)其中m是0,1或2;和(d)-CONR 3 R 4,其中R 3和R 4是H或C 1 -C 4烷基或与它们所连接的氮原子一起形成吡咯烷基, 哌啶子基,吗啉代或任选取代的哌嗪基。 该化合物可用作人和植物抗真菌剂。

    Triazole antifungal agents
    5.
    发明公开
    Triazole antifungal agents 失效
    三唑类抗真菌剂Wirkstoffe。

    公开(公告)号:EP0136063A2

    公开(公告)日:1985-04-03

    申请号:EP84305708.4

    申请日:1984-08-22

    摘要: Triazole antifungal agents of the formula:
    and their salts,

    where n is 0 or an integer of from 1 to 4, and X is selected from (a) optionally substituted phenoxy (b) optionally substituted
    heteroaryl-oxy (c) -S(O) m ·(C 1 -C 4 alkyl) where m is 0, 1 or 2 and (d) -CONR 3 R 4 where R 3 and R 4 are either H or C 1 -C 4 alkyl
    or together with the nitrogen atom to which they are attached form a pyrrolidinyl, piperidino, morpholino or optionally substituted piperazinyl group.

    The compounds are useful as human and plant antifungal agents.

    摘要翻译: 其中n为0或1至4的整数,X选自(​​a)任选取代的苯氧基1b)任选取代的杂芳基 - 氧基(C )-S(O)m(C 1 -C 4烷基),其中m为0,1或2和(d)-CONR 3 R 4,其中R 3和R 4为H或C 1 -C 1-4烷基或与它们所连接的氮原子一起形成吡咯烷基,哌啶子基,吗啉代或任选取代的哌嗪基。 该化合物可用作人和植物抗真菌剂。