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1. 发明授权

US4667041A Process for the preparation of 3-hydrazino-1,2-benz-isothiazole 1,1-dioxides 失效
标题翻译： 3-肼基-1,2-苯并异噻唑1,1-二氧化物的制备方法
公开(公告)号：US4667041A
公开(公告)日：1987-05-19
申请号：US706577
申请日：1985-02-28
申请人： Herbert Salzburg , Manfred Hajek , Gerd Hanssler
发明人： Herbert Salzburg , Manfred Hajek , Gerd Hanssler
IPC分类号： A01N43/80 , C07D275/06
CPC分类号： C07D275/06 , A01N43/80
摘要： A process for the preparation of a 3-hydrazino-1, 2-benzisothiazole 1,1-dioxide of the formula ##STR1## in which R.sup.1 and R.sup.2 each independently is hydrogen, alkyl, halogen, amino, hydroxyl or carboxyl, andR.sup.3 and R.sup.4 each independently is hydrogen, alkyl, cycloalkyl or aryl,comprising reacting a 3-keto-2H,3H-1,2-benzisothiazole 1,1-dioxide of the formula ##STR2## with a hydrazine of the formula ##STR3## in a molar ratio of 1:1 to 1:50, in an inert solvent, at a temperature between 75.degree. C. and 200.degree. C. and for a reaction time of 15 to 40 hours. The products, some of which are known, are fungicidally active and can also be used as intermediates.
摘要翻译：制备式“IMAGE”的3-肼基-1,2-苯并异噻唑1,1-二氧化物的方法，其中R 1和R 2各自独立地为氢，烷基，卤素，氨基，羟基或羧基，以及R 3和 R 4各自独立地是氢，烷基，环烷基或芳基，包括使式IMAGE的3-酮基-2H，3H-1,2-苯并异噻唑1,1-二氧化物与式IMAMA的肼反应摩尔比为1:1至1:50，在惰性溶剂中，在75℃至200℃之间，反应时间为15至40小时。其中一些已知的产品是杀真菌活性的并且也可以用作中间体。

2. 发明授权

US4713389A Fungicidally and bactericidally active acylated saccharin derivatives 失效
标题翻译：杀真菌和杀菌活性酰化糖精衍生物
公开(公告)号：US4713389A
公开(公告)日：1987-12-15
申请号：US774271
申请日：1985-09-10
申请人： Herbert Salzburg , Manfred Hajek , Hermann Hagemann , Engelbert Kuhle , Wolfgang Fuhrer , Gerd Hanssler , Wilhelm Brandes , Paul Reinecke
发明人： Herbert Salzburg , Manfred Hajek , Hermann Hagemann , Engelbert Kuhle , Wolfgang Fuhrer , Gerd Hanssler , Wilhelm Brandes , Paul Reinecke
IPC分类号： A01N47/38 , A61K31/425 , A61K31/428 , A61P31/04 , C07D275/06
CPC分类号： C07D275/06 , A01N47/38
摘要： Fungicidally and bactericidally active novel acylated saccharins of the formula ##STR1## in which X is oxygen or sulphur andR is --CO--R.sup.1 or --SO.sub.2 --OR.sup.2,R.sup.1 is alkyl, halogenalkyl, alkoxy, halogenoalkoxy or alkylthio, or is optionally substituted aryl, aryloxy or arylthio, cycloalkoxy or --NR.sup.3 R.sup.4,R.sup.2 is alkyl or phenyl,R.sup.3 is alkyl, andR.sup.4 is alkyl, phenyl, halogenoalkylthio, alkoxycarbonyl or phenoxycarbonyl, or--NR.sup.3 R.sup.4 is a saccharin radical.
摘要翻译：式中：X为氧或硫，R为-CO-R 1或-SO 2 OR 2的杀真菌杀菌活性新型酰化糖精，R1为烷基，卤代烷基，烷氧基，卤代烷氧基或烷硫基，或为任选取代的芳基芳氧基或芳硫基，环烷氧基或-NR3R4，R2是烷基或苯基，R3是烷基，R4是烷基，苯基，卤代烷硫基，烷氧基羰基或苯氧羰基，或-NR3R4是糖精基。

3. 发明授权

US4666930A 3-hydrazono-benzisothiazole 1,1-dioxide fungicides 失效
标题翻译： 3-肼基 - 苯并异噻唑1,1-二氧化物杀真菌剂
公开(公告)号：US4666930A
公开(公告)日：1987-05-19
申请号：US707361
申请日：1985-03-01
申请人： Herbert Salzburg , Manfred Hajek , Gerd Hanssler
发明人： Herbert Salzburg , Manfred Hajek , Gerd Hanssler
IPC分类号： A01N43/80 , A01N47/24 , A01N47/34 , C07D275/06 , C07D417/12
CPC分类号： C07D275/06 , A01N43/80 , A01N47/24 , A01N47/34 , C07D417/12
摘要： Compounds of the formula ##STR1## in which R.sup.1 is alkyl, cycloalkyl, aryl or hydrogen,R.sup.2 is --CO--R.sup.3,R.sup.3 is alkyl, alkenyl or cycloalkyl, or is phenyl which is optionally substituted, or is alkoxy or benzyl, or is phenoxy which is optionally substituted, or is phenoxymethyl, alkylamino, cycloalkylamino or phenylamino, orR.sup.1 and R.sup.2 together are a ##STR2## group, R.sup.4 and R.sup.5 each independently is hydrogen, alkyl, cycloalkenyl or phenylalkenyl, or is phenyl which is optionally substituted by alkyl, halogen and/or alkoxy, or is furyl, orR.sup.4 and R.sup.5 together are alkylene having 4 to 6 carbon atoms,are fungicidally active. Those compounds wherein R.sup.3 is alkylamino, cycloalkylamino or phenylamino, with the exception of the compound in which R.sup.1 is hydrogen and R.sup.6 is phenylamino, are new.
摘要翻译：式中，R 1为烷基，环烷基，芳基或氢的化合物，R 2为-CO-R 3，R 3为烷基，烯基或环烷基，或为任选取代的苯基，或为烷氧基或苄基，或为任选被取代的苯氧基，或者是苯氧基甲基，烷基氨基，环烷基氨基或苯基氨基，或者R 1和R 2一起是一个基团，R 4和R 5各自独立地是氢，烷基，环烯基或苯基烯基，或者是任选地被烷基，卤素和/或烷氧基，或是呋喃基，或R4和R5一起是具有4-6个碳原子的亚烷基，是杀真菌活性的。其中R 3是烷基氨基，环烷基氨基或苯基氨基的那些化合物，除了其中R 1是氢和R 6是苯基氨基的化合物外，是新的。

4. 发明授权

US4683233A Salts of 2-keto-2H, 3H-1,2-benzisothiazole 1,1-dioxide as microbicides 失效
公开(公告)号：US4683233A
公开(公告)日：1987-07-28
申请号：US704439
申请日：1985-02-22
申请人： Herbert Salzburg , Manfred Hajek , Gerd Hanssler , Varl-Heinz Kuck
发明人： Herbert Salzburg , Manfred Hajek , Gerd Hanssler , Varl-Heinz Kuck
IPC分类号： A01N47/44 , A01N20060101 , A01N37/44 , A01N43/16 , A01N43/40 , A01N43/50 , A01N43/54 , A01N43/56 , A01N43/60 , A01N43/653 , A01N43/76 , A01N43/80 , A01N43/84 , A01N43/90 , A01N47/42
CPC分类号： A01N43/56 , A01N37/44 , A01N43/16 , A01N43/40 , A01N43/50 , A01N43/54 , A01N43/60 , A01N43/653 , A01N43/76 , A01N43/80 , A01N43/84 , A01N43/90 , A01N47/44
摘要： A method of combating fungi and bacteria which comprises applying to such fungi, bacteria or a habitat thereof, a fungicidally or bactericidally effective amount of at least one salt of 3-keto-2-, 3H-1,2-benzisothiazole 1,1-dioxide of the formula ##STR1## in which R.sup.1 represents hydrogen, alkyl having 1 to 18 carbon atoms, or alkyl which has 1 to 6 carbon atoms and is optionally monosubstituted to trisubstituted by hydroxyl and/or monosubstituted to trisubstituted by amino, or represents carboxyl-substituted alkyl having 1 to 4 carbon atoms, or phenyl which is optionally monosubstituted to trisubstituted by identical or different substituents from amongst nitro and chlorine, or represents cycloalkyl having 5 or 6 carbon atoms, or represents heterocyclic structures which are optionally saturated or unsaturated, are optionally monosubstituted to tetrasubstituted by alkyl having 1 to 4 carbon atoms or hydroxyl, and have 1 to 3 identical or different heteroatoms, and a total of 5 or 6 ring members,R.sup.2 represents alkyl having 1 to 18 atoms, or alkyl which has 1 to 6 carbon atoms and is optionally monosubstituted to trisubstituted by hydroxyl and/or monosubstituted to trisubstituted by amino, or represents carboxyl-substituted alkyl having 1 to 4 carbon atoms, or phenyl which is optionally monosubstituted to trisubstituted by identical or different substituents from amongst nitro and chlorine, or represent cycloalkyl having 5 or 6 carbon atoms, or represents heterocyclic structures which are optionally saturated or unsaturated, are optionally monosubstituted to tetrasubstituted by alkyl having 1 to 4 carbon atoms or hydroxyl, and have 1 to 3 identical or different heteroatoms, and a total of 5 or 6 ring members, andR.sup.3 represents hydrogen, alkyl, having 1 to 6 carbon atoms, NH.sub.2, ##STR2## benzyl, or hydroxyalkyl having 1 to 3 carbon atoms, with the exception of the mono-, di- and triethanolamine compounds, orR.sup.1 and R.sup.2 together with the nitrogen atom at which they are located, form a 5-membered or 6-membered ring which can optionally contain further heteroatoms, and can optionally be substituted by keto groups or fused-on 5-membered or 6-membered rings and/or alkyl having 1 to 4 carbon atoms, with the exception of the pyridine ring which is optionally mono- or disubstituted by methyl.

5. 发明申请

US20080113864A1 (-)-Enantiomer of the 2-[2-(1-chloro-cyclopropyl)-3-(2-chlorophenyl)-2-hydroxypropyl]-2,4-dihydro-[1,2,4]-triazole-3-thione 有权
标题翻译：（ - ） - 2- [2-（1-氯 - 环丙基）-3-（2-氯苯基）-2-羟丙基] -2,4-二氢 - [1,2,4] - 三唑-3 - 硫酮
公开(公告)号：US20080113864A1
公开(公告)日：2008-05-15
申请号：US11981050
申请日：2007-10-31
申请人： Rolf Grosser , Manfred Jautelat , Astrid Mauler-Machnik , Stefan Dutzmann , Gerd Hanssler , Klaus Stenzel
发明人： Rolf Grosser , Manfred Jautelat , Astrid Mauler-Machnik , Stefan Dutzmann , Gerd Hanssler , Klaus Stenzel
IPC分类号： A01N43/653 , C07D249/12 , A01P3/00 , A01P13/00 , A01P1/00
CPC分类号： C07D249/12 , A01N43/653
摘要： A novel (−)-enantiomer of 2-[2-(1-chloro-cyclopropyl)-3-(2-chloro-phenyl)-2-hydroxypropyl]-2,4-dihydro-[1,2,4]-triazole-3-thione of the formula a process for preparing this novel active compound and its use as microbicide in crop protection and in the protection of materials.
摘要翻译： 2- [2-（1-氯 - 环丙基）-3-（2-氯 - 苯基）-2-羟丙基] -2,4-二氢 - [1,2,4] - 三唑-3-硫酮的制备方法，该方法用于制备该新型活性化合物及其作为杀菌剂在作物保护和材料保护中的用途。

6. 发明授权

US6130251A Alkoximinoacetic acid amides 失效
标题翻译：铝肟酸酰胺
公开(公告)号：US6130251A
公开(公告)日：2000-10-10
申请号：US875300
申请日：1997-07-23
申请人： Thomas Seitz , Gerd Hanssler , Klaus Stenzel
发明人： Thomas Seitz , Gerd Hanssler , Klaus Stenzel
IPC分类号： C07D239/26 , A01N37/00 , A01N37/18 , A01N37/22 , A01N37/50 , A01N43/08 , A01N43/10 , A01N43/12 , A01N43/38 , A01N43/40 , A01N43/54 , A01N43/78 , C07C251/48 , C07C255/44 , C07C255/62 , C07C323/63 , C07D209/14 , C07D209/42 , C07D213/40 , C07D277/20 , C07D277/32 , C07D307/02 , C07D307/54 , C07D333/04 , C07D333/20 , C07D333/24 , C07D333/28 , C07D333/32 , C07D333/58 , C07D333/68 , C07D333/70 , C07C233/05
CPC分类号： C07D277/20 , A01N37/50 , A01N43/08 , A01N43/10 , A01N43/12 , A01N43/38 , A01N43/40 , A01N43/54 , A01N43/78 , C07C251/48 , C07C255/44 , C07C255/62 , C07C323/63 , C07D209/42 , C07D307/54 , C07D333/24 , C07D333/68 , C07D333/70 , C07C2101/02 , C07C2101/14
摘要： The invention relates to new alkoximinoacetic acid amides, a process for their preparation and their use as agents for combating pests.
摘要翻译： PCT No.PCT / EP96 / 00179 Sec。 371日期1997年7月23日 102（e）1997年7月23日PCT PCT 1996年1月17日PCT公布。 WO96 / 23763 PCT出版物日期1996年8月8日本发明涉及新的肟基乙酰胺，其制备方法及其作为防治害虫的药剂。

7. 发明授权

US5942528A Acylated 5-amino-1,2,4-thiadiazoles as pesticides and fungicides 失效
标题翻译：酰化5-氨基-1,2,4-噻二唑作为农药和杀真菌剂
公开(公告)号：US5942528A
公开(公告)日：1999-08-24
申请号：US101116
申请日：1998-06-30
申请人： Markus Heil , Christoph Erdelen , Ulrike Wachendorff-Neumann , Andreas Turberg , Norbert Mencke , Gerd Hanssler , Klaus Stenzel
发明人： Markus Heil , Christoph Erdelen , Ulrike Wachendorff-Neumann , Andreas Turberg , Norbert Mencke , Gerd Hanssler , Klaus Stenzel
IPC分类号： A01N43/82 , A01N43/836 , C07D285/08
CPC分类号： C07D285/08 , A01N43/82
摘要： The present invention relates to novel acylated 5-amino-1,2,4-thiadiazoles of the formula (I) ##STR1## in which R.sup.1, R.sup.2, R.sup.3 and Y each have the meanings stated in the description,a process for their preparation, and to their use for controlling animal pests.
摘要翻译： PCT No.PCT / EP97 / 00012 Sec。 371日期1998年6月30日第 102（e）1998年6月30日日期PCT 1997年1月3日PCT PCT。公开号WO97 / 26251 日期1997年7月24日本发明涉及式（I）的新型酰化5-氨基-1,2,4-噻二唑，其中R1，R2，R3和Y各自具有说明书中所述的含义，他们的准备以及用于控制动物害虫的用途。

8. 发明授权

US5883250A Substituted azadioxacycloalkenes, fungicidal composition containing them, process for preparing them, and method of using them to combat fungi 失效
标题翻译：取代的azadioxacycalkalkene，含有它们的杀真菌组合物，其制备方法和使用它们对抗真菌的方法
公开(公告)号：US5883250A
公开(公告)日：1999-03-16
申请号：US857119
申请日：1997-05-15
申请人： Bernd-Wieland Kruger , Lutz Assmann , Herbert Gayer , Peter Gerdes , Ulrich Heinemann , Dietmar Kuhnt , Ulrich Philipp , Thomas Seitz , Jorg Stetter , Ralf Tiemann , Heinz-Wilhelm Dehne , Stefan Dutzmann , Gerd Hanssler
发明人： Bernd-Wieland Kruger , Lutz Assmann , Herbert Gayer , Peter Gerdes , Ulrich Heinemann , Dietmar Kuhnt , Ulrich Philipp , Thomas Seitz , Jorg Stetter , Ralf Tiemann , Heinz-Wilhelm Dehne , Stefan Dutzmann , Gerd Hanssler
IPC分类号： A01N43/72 , A01N43/78 , A01N43/836 , A01N43/88 , C07D273/00 , C07D273/01 , C07D409/12 , C07D413/06 , C07D413/12 , C07D413/14 , C07D417/12 , C07D417/14 , C07D273/06 , C07D269/00
CPC分类号： C07D273/00 , A01N43/88 , C07D409/12 , C07D413/06 , C07D413/12 , C07D413/14 , C07D417/12 , C07D417/14
摘要： New azadioxacycloalkenes of the formula (I): ##STR1## wherein Z, G, Ar, E and A are as defined herein, fungicidal compositions containing them, processes for preparing them, and methods of using them to combat fungi.
摘要翻译：式（I）的新的氮杂二环烷基烯烃：其中Z，G，Ar，E和A如本文所定义，含有它们的杀真菌组合物，其制备方法和使用它们来对抗真菌的方法。

9. 发明授权

US5530149A Azolylmethyl-fluorocyclopropyl derivatives 失效
公开(公告)号：US5530149A
公开(公告)日：1996-06-25
申请号：US462730
申请日：1995-06-05
申请人： Jurgen Scherkenbeck , Thomas Himmler , Stefan Bohm , Hermann Hagemann , Klaus Stroech , Stefan Dutzmann , Heinz-Wilhelm Dehne , Gerd Hanssler
发明人： Jurgen Scherkenbeck , Thomas Himmler , Stefan Bohm , Hermann Hagemann , Klaus Stroech , Stefan Dutzmann , Heinz-Wilhelm Dehne , Gerd Hanssler
IPC分类号： A01N43/653 , C07D249/08 , C07D301/02 , C07D303/08 , C07D303/18 , C07D303/20 , C07D521/00
CPC分类号： C07D249/08 , A01N43/653 , C07D231/12 , C07D233/56
摘要： New azolylmethyl-fluorocyclopropyl derivatives of the formula ##STR1## in which R represents ##STR2## and addition products thereof which acids or metal salts are very effective for combating fungi.New oxiranes of the formula ##STR3## in which R has the abovementioned meaning, are valuable intermediates for the preparation of compounds of the formula (I).

10. 发明授权

US5334608A Azolymethyl-cyclopropyl derivatives 失效
标题翻译：芳基甲基 - 环丙基衍生物
公开(公告)号：US5334608A
公开(公告)日：1994-08-02
申请号：US021390
申请日：1993-02-23
申请人： Jurgen Scherkenbeck , Thomas Himmler , Hermann Hagemann , Stefan Dutzmann , Heinz-Wilhelm Dehne , Gerd Hanssler
发明人： Jurgen Scherkenbeck , Thomas Himmler , Hermann Hagemann , Stefan Dutzmann , Heinz-Wilhelm Dehne , Gerd Hanssler
IPC分类号： A01N53/12 , A01N43/653 , A01N53/04 , A61K31/41 , C07D249/08 , C07D301/02 , C07D303/46 , C07D521/00
CPC分类号： C07D249/08 , A01N43/653 , C07D231/12 , C07D233/56 , C07D303/46
摘要： New azolylmethyl-cyclopropyl derivatives of the formula ##STR1## in which R represents cyano or a group of the formula ##STR2## Z represents halogen, alkyl having 1 to 4 carbon atoms, halogenoalkyl having 1 to 4 carbon atoms and 1 to 5 halogen atoms, alkoxy having 1 to 4 carbon atoms, halogenoalkoxy having 1 to 4 carbon atoms and 1 to 5 halogen atoms, or alkoximininoalkyl having 1 to 4 carbon atoms in the alkoxy group and 1 to 4 carbon atoms in the alkyl group andm represents the numbers 0, 1 or 2, and addition products thereof with acids or metal salts are very effective for combating fungi.New oxiranes of the formula ##STR3## in which Z and m have the abovementioned meanings, are valuable intermediates for the preparation of compounds of the formula (I).
摘要翻译：其中R表示氰基的式（I）的新的唑基甲基 - 环丙基衍生物或下式的基团Z表示卤素，具有1至4个碳原子的烷基，具有1至4个碳原子的卤代烷基和1至 5个卤素原子，1〜4个碳原子的烷氧基，1〜4个碳原子的卤代烷氧基和1〜5个卤素原子，烷氧基中1〜4个碳原子的烷基肟基，烷基中1〜4个碳原子代表数字0,1或2，其与酸或金属盐的加成产物对抗真菌非常有效。其中Z和m具有上述含义的式“IMAGE”（II）的新环氧烷是制备式（I）化合物的有价值的中间体。

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