Substituted thiophenecarboxamides
    1.
    发明授权
    Substituted thiophenecarboxamides 失效
    取代的噻吩甲酰胺

    公开(公告)号:US5369124A

    公开(公告)日:1994-11-29

    申请号:US126821

    申请日:1993-09-24

    CPC分类号: C07D333/38 A01N43/10

    摘要: Novel substituted thiophenecarboxamides of the formula (I), ##STR1## in which R represents hydrogen or alkyl,A represents doubly linked alkanediyl,Ar represents optionally substituted aryl andn represents a number 0 or 1,with the exception of the compounds 4,5-dibromo-thiophene-2-carboxylic acid N-(4-bromophenyl)-amide, 4,5-dibromo-thiophene-2-carboxylic acid N-(2,3-dichlorophenyl)-amide and 4,5-dibromo-thiophene-2-carboxylic acid N-[2-(3,4-dimethoxyphenyl)-ethyl]-amide, and their use for combating pests.The novel compounds are described by the formula (I) and they can be prepared by analogous processes, e.g. by reacting suitable thiophenecarbonyl halides with suitable amines.

    摘要翻译: 式(I)的新型取代的噻吩甲酰胺,其中R表示氢或烷基,其中R表示氢或烷基,A表示双链烷二基,Ar表示任选取代的芳基,n表示0或1,除了化合物 4,5-二溴 - 噻吩-2-甲酸N-(4-溴苯基) - 酰胺,4,5-二溴 - 噻吩-2-甲酸N-(2,3-二氯苯基) - 酰胺和4,5-二溴 - 二溴 - 噻吩-2-羧酸N- [2-(3,4-二甲氧基苯基) - 乙基] - 酰胺及其用于防治害虫的用途。 新化合物由式(I)描述,它们可以通过类似方法制备,例如 通过使合适的噻吩羰基卤化物与合适的胺反应。

    Microbicidal compositions based on dibromo-thiophene-carboxylic acid
derivatives
    2.
    发明授权
    Microbicidal compositions based on dibromo-thiophene-carboxylic acid derivatives 失效
    基于二溴 - 噻吩 - 羧酸衍生物的杀菌组合物

    公开(公告)号:US5789437A

    公开(公告)日:1998-08-04

    申请号:US722262

    申请日:1996-10-04

    CPC分类号: A01N43/10 C07D333/38

    摘要: New microbicidal compositions based on dibromo-thiophene-carboxylic acid derivatives which are known in some cases, of the formula ##STR1## in which R represents the groups --XR.sup.1, --NR.sup.2 R.sup.3, --NR.sup.4 OR.sup.5 or --NR.sup.4 --N(R.sup.5).sub.2, where X represents oxygen or sulphur and R.sup.1, R.sup.2, R.sup.3, R.sup.4 and R.sup.5 have the meanings indicated in the description, and the use of these substances for controlling undesired microorganisms. New dibromo-thiophene-carboxylic acid derivatives of the formula ##STR2## in which R.sup.9 represents the groups --SR.sup.1, --OR.sup.10, ##STR3## in which R.sup.1, R.sup.4, R.sup.5, R.sup.10, R.sup.11, R.sup.12 and R.sup.13 have the meaning indicated in the description, and processes for the preparation of the substances of the formula (I-A).

    摘要翻译: PCT No.PCT / EP95 / 01173 Sec。 371日期1996年10月4日第 102(e)日期1996年10月4日PCT 1995年3月29日PCT PCT。 WO95 / 27397 PCT出版物 日期1995年10月19日新的一些基于二溴 - 噻吩 - 羧酸衍生物的杀微生物组合物,其在一些情况下是式(I),其中R表示基团-XR1,-NR2R3,-NR4OR5或-NR4 -N(R5)2,其中X表示氧或硫,R1,R2,R3,R4和R5具有说明书中指出的含义,以及这些物质用于防治不需要的微生物的用途。 式(IA)的新的二溴 - 噻吩 - 羧酸衍生物,其中R9代表基团-SR1,-OR10,其中R1,R4,R5,R10,R11,R12和R13具有含义 在说明书中指出,以及制备式(IA)的物质的方法。

    Fungicidal
4-(4-substituted-phenyl)-3,3-dimethyl-2-(3-pyridyl)-butan-2-ol derivativ
es
    5.
    发明授权
    Fungicidal 4-(4-substituted-phenyl)-3,3-dimethyl-2-(3-pyridyl)-butan-2-ol derivativ es 失效
    杀真菌剂4-(4-取代苯基)-3,3-二甲基-2-(3-吡啶基) - 丁-2-醇衍生物

    公开(公告)号:US5036073A

    公开(公告)日:1991-07-30

    申请号:US442042

    申请日:1989-11-28

    摘要: Fungicidal substituted pyridine derivatives of the formula ##STR1## in which Ar stands for optionally substituted aryl,X stands for oxygen, sulphur, sulphinyl, sulphonyl or for one of the groups --CH.sub.2 --; --O--CH.sub.2 --; --CH.sub.2 --O--; --O--CH.sub.2 --CH.sub.2 --; --S(O).sub.n --CH.sub.2 --; --CH.sub.2 --S(O).sub.n -- or --S(O).sub.n --CH.sub.2 --CH.sub.2 --,in whichn in each case stands for the number 0, 1 or 2,R stands for alkyl, alkenyl, alkinyl, alkoxyalkyl, alkylthioalkyl, cycloalkyl, cycloalkylalkyl or for in each case optionally substituted aryl, aralkyl, aryloxyalkyl or arylthioalkyl andm stands for the number 0 or 1,and plant-compatible acid and metal salt addition products thereof. Intermediates of the formula ##STR2## are also new.

    摘要翻译: 式(I)的杀真菌取代的吡啶衍生物,其中Ar表示任选取代的芳基,X表示氧,硫,亚磺酰基,磺酰基或基团-CH 2 - 之一; -O-CH 2 - ; -CH 2 -O-; -O-CH 2 -CH 2 - ; -S(O)n -CH 2 - ; -CH 2 -S(O)n - 或-S(O)n -CH 2 -CH 2 - ,其中n表示数字0,1或2,R表示烷基,烯基,炔基,烷氧基烷基,烷硫基烷基 ,环烷基,环烷基烷基或在各种情况下任选取代的芳基,芳烷基,芳氧基烷基或芳硫基烷基,m代表数字0或1,以及与植物相容的酸和金属盐加成产物。 式(IMA)(VI)的中间体也是新的。