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61. 发明授权

US4382944A Combating fungi with 1-phenoxy-1-triazolyl-3-fluoromethyl-butane derivatives 失效
标题翻译：抗真菌与1-苯氧基-1-三唑基-3-氟甲基 - 丁烷衍生物
公开(公告)号：US4382944A
公开(公告)日：1983-05-10
申请号：US307838
申请日：1981-10-02
申请人： Wolfgang Kramer , Karl H. Buchel , Jorg Stetter , Paul-Ernst Frohberger , Wilhelm Brandes , Hans Scheinpflug
发明人： Wolfgang Kramer , Karl H. Buchel , Jorg Stetter , Paul-Ernst Frohberger , Wilhelm Brandes , Hans Scheinpflug
IPC分类号： A01N43/653 , C07C45/63 , C07C45/67 , C07C45/71 , C07C49/16 , C07C49/167 , C07C49/255 , C07D233/60 , C07D249/08 , C07D521/00 , A01N43/64 , A01N55/02 , C07F3/00
CPC分类号： C07D231/12 , A01N43/653 , C07C45/63 , C07C45/673 , C07C45/71 , C07C49/16 , C07C49/167 , C07C49/255 , C07D233/56 , C07D249/08
摘要： 1-Phenoxy-1-triazolyl-3-fluoromethyl-butane derivatives of the formula ##STR1## in which Az is 1,2,4-triazol-1-yl or 1,2,4-triazol-4-yl,B is --CO-- or --CH(OH)--,X is hydrogen or fluorine,Z each independently is halogen, alkyl, nitro, cyano, alkoxy-carbonyl or optionally substituted phenyl, andn is 0, 1, 2 or 3,or an acid or metal salt adduct thereof which possess fungicidal properties.
摘要翻译：其中Az是1,2,4-三唑-1-基或1,2,4-三唑-4-基的式“IMAGE”的1-苯氧基-1-三唑基-3-氟甲基 - 丁烷衍生物，B是 -CO-或-CH（OH） - ，X为氢或氟，Z各自独立地为卤素，烷基，硝基，氰基，烷氧基 - 羰基或任选取代的苯基，n为0,1,2或3，或其酸或金属盐加合物具有杀真菌性能。

62. 发明授权

US4366152A Combatting fungi with metal salt complexes of 1-phenyl-2-(1,2,4-triazol-1-yl)-ethanes 失效
标题翻译：将真菌与1-苯基-2-（1,2,4-三唑-1-基） - 乙胺的金属盐络合物作用
公开(公告)号：US4366152A
公开(公告)日：1982-12-28
申请号：US909602
申请日：1978-05-25
申请人： Wolfgang Kramer , Helmut Timmler , Karl H. Buchel , Wilhelm Brandes , Paul-Ernst Frohberger , Hans Scheinpflug
发明人： Wolfgang Kramer , Helmut Timmler , Karl H. Buchel , Wilhelm Brandes , Paul-Ernst Frohberger , Hans Scheinpflug
IPC分类号： A01N43/653 , A01P3/00 , C07D249/08 , C07D521/00 , A01N55/02 , A01N55/04 , C07F1/08
CPC分类号： C07D231/12 , A01N43/653 , C07D233/56 , C07D249/08
摘要： Combating fungi with metal salt complexes of 1-phenyl-2-(1,2,4-triazol-1-yl)-ethanes of the formula ##STR1## in which R represents halogen, alkyl, alkoxy, alkylthio, alkylsulphonyl, halogenoalkyl, nitro, cyano, optionally substituted phenyl or optionally substituted phenoxy,R.sup.1 represents the grouping --O--R.sup.2, --S(O).sub.m --R.sup.3 or --O--CO--R.sup.4,R.sup.2 represents alkyl, alkenyl, alkynyl, cycloalkyl, optionally substituted aryl, optionally substituted araylalkyl or optionally substituted arylalkenyl,R.sup.3 represents hydrogen, alkyl, alkenyl, alkynyl, cycloalkyl, optionally substituted aryl, optionally substituted arylalkyl or optionally substituted arylalkenyl,R.sup.4 represents alkyl, alkenyl, alkynyl, cycloalkyl, optionally substituted aryl, optionally substituted arylalkyl, optionally substituted arylalkenyl, halogenoalkyl, optionally substituted phenoxyalkyl, amino, alkylamino, dialkylamino, alkyl-alkylcarbonylamino or optionally substituted phenylamino,A represents an anion of an inorganic acid,M represents a metal,n represents 0, 1, 2, 3, 4 or 5,m represents 0, 1 or 2,p represents 1, 2, 3, 4, 5 or 6, andx represents 1, 2, 3 or 4which possess fungicidal properties.
摘要翻译：将真菌与式（IMAGE）的1-苯基-2-（1,2,4-三唑-1-基） - 乙胺的金属盐络合物相互作用，其中R表示卤素，烷基，烷氧基，烷硫基，烷基磺酰基，卤代烷基，硝基，氰基，任选取代的苯基或任选取代的苯氧基，R 1表示分组-O-R 2，-S（O）m -R 3或-O-CO-R 4，R 2表示烷基，烯基，炔基，环烷基，任选取代的芳基，任选取代的芳烷基或任选取代的芳基烯基，R 3表示氢，烷基，烯基，炔基，环烷基，任选取代的芳基，任选取代的芳基烷基或任选取代的芳基烯基，R 4表示烷基，烯基，炔基，环烷基，任选取代的芳基，，任选取代的芳基烯基，卤代烷基，任选取代的苯氧基烷基，氨基，烷基氨基，二烷基氨基，烷基 - 烷基羰基氨基或任选取代的苯基氨基，A表示无机酸的阴离子，M表示 ts为金属，n表示0,1,2,3,4或5，m表示0,1或2，p表示1,2,3,4,5或6，x表示1,2,3或4 具有杀菌性。

63. 发明授权

US4360529A Combating fungi with trisubstituted benzyl oxime ethers 失效
标题翻译：抗真菌与三取代苄基肟醚
公开(公告)号：US4360529A
公开(公告)日：1982-11-23
申请号：US201863
申请日：1980-10-29
申请人： Wolfgang Kramer , Hans-Joachim Knops , Karl H. Buchel , Wilhelm Brandes , Paul-Ernst Frohberger
发明人： Wolfgang Kramer , Hans-Joachim Knops , Karl H. Buchel , Wilhelm Brandes , Paul-Ernst Frohberger
IPC分类号： A01N43/64 , A01N43/653 , C07D249/08 , C07D405/12 , C07D521/00 , A01N55/02 , C07F1/08
CPC分类号： C07D231/12 , A01N43/653 , C07D233/56 , C07D249/08
摘要： Combating fungi with a trisubstituted benzyl oxime ether of the formula ##STR1## in which R is halogen, alkyl or halogenoalkyl,n is 1, 2 or 3, andX, Y and Z each independently is alkyl, alkoxy or halogen, or Y and Z together are methylenedioxy,or a physiologically acceptable acid-addition salt or metal-salt complex thereof.
摘要翻译：将真菌与式“IMAGE”的三取代苄基肟醚反应，其中R为卤素，烷基或卤代烷基，n为1,2或3，X，Y和Z各自独立地为烷基，烷氧基或卤素，或Y和 Z一起是亚甲二氧基，或其生理上可接受的酸加成盐或金属盐络合物。

64. 发明授权

US4316932A Combating fungi with .alpha.-azolyl-keto derivatives 失效
标题翻译：抗真菌与α-唑基 - 酮衍生物
公开(公告)号：US4316932A
公开(公告)日：1982-02-23
申请号：US54067
申请日：1979-07-02
申请人： Eckart Kranz , Wolfgang Kramer , Karl H. Buchel , Wilhelm Brandes , Paul-Ernst Frohberger
发明人： Eckart Kranz , Wolfgang Kramer , Karl H. Buchel , Wilhelm Brandes , Paul-Ernst Frohberger
IPC分类号： A01N43/50 , A01N43/653 , C07D233/60 , C07D249/08 , C07D521/00 , A01N43/82
CPC分类号： C07D231/12 , A01N43/50 , A01N43/653 , C07D233/56 , C07D249/08
摘要： An .alpha.-azolyl-keto derivative of the formula ##STR1## in which R.sup.1 represents optionally substituted alkyl or optionally substituted phenyl,R.sup.2 represents the grouping --CX.sup.1 X.sup.2 R.sup.3 or alkoxy-carbonyl,R.sup.3 represents halogen, halogenoalkyl or optionally substituted phenyl,R.sup.4 represents the grouping --O--CO--R.sup.5, --O(S)--R.sup.6 or --O--S(O).sub.n --R.sup.7, or alkylamino, dialkylamino, optionally substituted phenylamino or halogen,R.sup.5 represents alkyl, halogenoalkyl, alkenyl, alkynyl, cycloalkyl, optionally substituted phenyl, optionally substituted phenylalkyl, alkylamino, dialkylamino or optionally substituted phenylamino,R.sup.6 represents alkyl, alkenyl, alkynyl, cycloalkyl, optionally substituted phenyl or optionally substituted benzyl,R.sup.7 represents alkyl, halogenoalkyl, optionally substituted phenyl or dialkylamino,n represents 1 or 2,X.sup.1 and X.sup.2 each independently represents hydrogen or halogen, andY represents a nitrogen atom or the CH group, or a physiologically acceptable acid addition salt or metal salt complex thereof, which possesses fungicidal properties.
摘要翻译：其中R 1表示任意取代的烷基或任意取代的苯基，R 2代表基团-CX 1 X 2 R 3或烷氧基 - 羰基，R 3表示卤素，卤代烷基或任意取代的苯基，R 4代表基团 -O-CO-R 5，-O（S）-R 6或-OS（O）n -R 7或烷基氨基，二烷基氨基，任选取代的苯基氨基或卤素，R 5表示烷基，卤代烷基，烯基，炔基，环烷基，任选取代的苯基，任选取代的苯基烷基，烷基氨基，二烷基氨基或任选取代的苯基氨基，R 6表示烷基，烯基，炔基，环烷基，任选取代的苯基或任选取代的苄基，R 7表示烷基，卤代烷基，任选取代的苯基或二烷基氨基，n表示1或2，和X2各自独立地表示氢或卤素，Y表示氮原子或CH基团，或生理上可接受的酸加成盐或金属盐c 其复合物具有杀真菌性能。

65. 发明授权

US4283406A Combating Botrytis fungi with 1-(2,4-dichlorophenyl)-1-(2,6-dihalogenobenzyloximino)-2-(1,2,4-triazol- 1-yl)-ethanes 失效
标题翻译：将Botrytis真菌与1-（2,4-二氯苯基）-1-（2,6-二卤代苄基肟基）-2-（1,2,4-三唑-1-基） - 乙胺
公开(公告)号：US4283406A
公开(公告)日：1981-08-11
申请号：US141834
申请日：1980-04-21
申请人： Wolfgang Kramer , Hans-Joachim Knops , Karl H. Buchel , Wilhelm Brandes
发明人： Wolfgang Kramer , Hans-Joachim Knops , Karl H. Buchel , Wilhelm Brandes
IPC分类号： A01N43/653 , C07D249/08 , C07D521/00 , A01N43/64
CPC分类号： C07D231/12 , A01N43/653 , C07D233/56 , C07D249/08
摘要： A method of combating Botrytis fungi, comprising applying to such fungi, or to a habitat thereof to be protected against such fungus a fungicidally effective amount of a 1-(2,4-dichlorophenyl)-1-(2,6-dihalogenobenzyloximino)-2-(1,2,4-triazol-1-yl)-ethane of the formula ##STR1## in which X and Y each independently is halogen or a physiologically acceptable acid addition salt thereof. Those compounds in which X is chlorine or fluorine and Y is fluorine are new.
摘要翻译：一种抗葡萄孢菌真菌的方法，其包括向这种真菌施用或其栖息地保护免受这种真菌的杀真菌有效量的1-（2,4-二氯苯基）-1-（2,6-二卤代苯甲酰亚氨基） - 2-（1,2,4-三唑-1-基） - 乙烷，其中X和Y各自独立地为卤素或其生理上可接受的酸加成盐。其中X为氯或氟且Y为氟的化合物是新的。

66. 发明授权

US4237142A Combating fungi with 2-carbamoyloxy-3,3-dimethyl-1-phenoxy-1-(1,2,4-tri azol-1-yl)-1-butanes 失效
标题翻译：将2-氨基甲酰氧基-3,3-二甲基-1-苯氧基-1-（1,2,4-三唑-1-基）-1-丁烷与2-氨基甲酰氧基
公开(公告)号：US4237142A
公开(公告)日：1980-12-02
申请号：US971291
申请日：1978-12-20
申请人： Karl H. Buchel , Wolfgang Kramer , Wilhelm Brandes
发明人： Karl H. Buchel , Wolfgang Kramer , Wilhelm Brandes
IPC分类号： A01N43/653 , A01N47/12 , A01N47/20 , A01N47/24 , A01N57/00 , A01P3/00 , B01J27/00 , C07D233/60 , C07D249/08 , C07D521/00 , A01N43/64
CPC分类号： C07D231/12 , A01N47/12 , A01N47/20 , A01N47/24 , C07D233/56 , C07D249/08
摘要： 2-Carbamoyloxy-3,3-dimethyl-1-phenoxy-1-(1,2,4-triazol-1-yl)-1-butanes of the formula ##STR1## in which R is alkyl, halogenoalkyl, alkoxycarbonyl, alkoxyalkyl, substituted phenyl or alkylsulphonyl-alkenyl-carbamoyl,X each independently is halogen, alkyl, cycloalkyl, alkoxy, halogenoalkyl, alkylthio, alkoxycarbonyl, optionally substituted phenyl, optionally substituted phenoxy, optionally substituted phenylalkyl, amino, cyano or nitro, andn is 0, 1, 2, 3, 4 or 5,as the free base, salt or metal salt complex thereof which possess fungicidal properties.
摘要翻译：具有式“IMAGE”的2-氨基甲酰氧基-3,3-二甲基-1-苯氧基-1-（1,2,4-三唑-1-基）-1-丁烷，其中R是烷基，卤代烷基，烷氧基羰基，烷氧基烷基取代的苯基或烷基磺酰基 - 烯基 - 氨基甲酰基，X各自独立地为卤素，烷基，环烷基，烷氧基，卤代烷基，烷硫基，烷氧基羰基，任选取代的苯基，任选取代的苯氧基，任选取代的苯基烷基，氨基，氰基或硝基，n为0 ，1,2,3,4或5，作为其具有杀真菌性质的游离碱，其盐或金属盐络合物。

67. 发明授权

US4147791A 1-Substituted-1,2,4-triazole fungicidal compositions and methods for combatting fungi that infect or attack plants 失效
标题翻译： 1-取代的-1,2,4-三唑杀真菌组合物和用于对抗感染或攻击植物的真菌的方法
公开(公告)号：US4147791A
公开(公告)日：1979-04-03
申请号：US550242
申请日：1975-02-14
申请人： Werner Meiser , Karl H. Buchel , Wolfgang Kramer , Ferdinand Grewe
发明人： Werner Meiser , Karl H. Buchel , Wolfgang Kramer , Ferdinand Grewe
IPC分类号： C07D249/08 , A01N9/22 , A01N21/00
CPC分类号： C07D249/08
摘要： 1-SUBSTITUTED-1,2,4-TRIAZOLES OF THE FORMULA ##STR1## in which X.sup.1 represents hydrogen or an alkyl radical,X.sup.2 represents hydrogen or an alkyl radical,R.sup.1 represents an alkyl, alkenyl, alkynyl, cycloalkyl, cycloalkenyl or optionally substituted aryl or aralkyl radical,R.sup.2 represents hydrogen or an alkyl, alkenyl, alkynyl, cycloalkyl, cycloalkenyl or optionally substituted aryl or aralkyl radical,R.sup.3 represents hydrogen or an alkyl, alkenyl, alkynyl, cycloalkyl, cycloalkenyl or optionally substituted aryl or aralkyl radical, andY represents a keto group or a functional keto derivative, which possess fungicidal properties.
摘要翻译：其中X 1表示氢或烷基，X 2表示氢或烷基，R 1表示烷基，烯基，炔基，环烷基，环烯基（C 1 -C 6）的1-取代的1,2,4-三唑或任选取代的芳基或芳烷基，R 2表示氢或烷基，烯基，炔基，环烷基，环烯基或任选取代的芳基或芳烷基，R 3表示氢或烷基，烯基，炔基，环烷基，环烯基或任选取代的芳基或芳烷基基团，Y表示具有杀真菌性质的酮基或官能酮衍生物。

68. 发明授权

US4145428A Fungicidally active 2-acyloxy-1-phenoxy-1-(1,2,4-triazolyl)-3,3-dimethyl-butanes 失效
标题翻译：杀真菌剂2-氰基-1-苯氧基-1-（1,2,4-三唑基）-3,3-二甲基丁烷
公开(公告)号：US4145428A
公开(公告)日：1979-03-20
申请号：US753651
申请日：1976-12-21
申请人： Wolfgang Kramer , Karl H. Buchel , Wilhelm Brandes , Paul-Ernst Frohberger
发明人： Wolfgang Kramer , Karl H. Buchel , Wilhelm Brandes , Paul-Ernst Frohberger
IPC分类号： A01N43/653 , A01P3/00 , C07D233/60 , C07D249/08 , C07D521/00 , A01N9/22 , A61K31/41 , C07D249/10
CPC分类号： C07D231/12 , C07D233/56 , C07D249/08
摘要： 1-Phenoxy-1-(1,2,4-triazolyl)-3,3-dimethyl-butanes of the formula ##STR1## in which R represents alkyl, alkenyl, alkynyl, cycloalkyl, halogenoalkyl, optionally substituted phenyl, optionally substituted phenoxyalkyl, alkylamino, dialkylamino or optionally substituted phenylamino, X represents halogen, alkyl, cycloalkyl, alkoxy, halogenoalkyl, alkylthio, alkoxycarbonyl, optionally substituted phenyl, optionally substituted phenoxy, optionally substituted phenylalkyl, amino, cyano or nitro, N represents 0, 1, 2, 3, 4 or 5, and Az represents the 1,2,4-triazolyl-1 or the 1,2,4-triazolyl-4 radical, In the form of the free base, a salt with a physiologically tolerated acid or a complex with a metal salt, which possess fungicidal properties.

69. 发明授权

US4079142A 1-Propyl-triazolyl antimycotic compositions and methods of treating mycoses 失效
标题翻译： 1-丙基 - 三唑基抗真菌组合物和治疗真菌病的方法
公开(公告)号：US4079142A
公开(公告)日：1978-03-14
申请号：US638754
申请日：1975-12-08
申请人： Karl Heinz Buchel , Wolfgang Kramer , Manfred Plempel
发明人： Karl Heinz Buchel , Wolfgang Kramer , Manfred Plempel
IPC分类号： C07D249/08 , A61K31/41
CPC分类号： C07D249/08
摘要： Pharmaceutical compositions are produced which comprise an antimycotically effective amount of a compound of the formula ##STR1## or a pharmaceutically acceptable non-toxic salt thereof wherein R.sup.1 is an unsubstituted or substituted aryl moiety,R.sup.2 is hydrogen, alkyl, alkenyl, cycloalkyl, unsubstituted or substituted aryl or unsubstituted or substituted aralkyl, andR.sup.3 is hydrogen, alkyl or cycloalkyl,Provided that when R.sup.3 is hydrogen, R.sup.2 cannot be hydrogen, in combination with a pharmaceutically acceptable non-toxic inert diluent or carrier.
摘要翻译：制备药物组合物，其包含抗真菌有效量的下式化合物或其药学上可接受的无毒盐，其中R 1是未取代或取代的芳基部分，R 2是氢，烷基，烯基，环烷基，未取代的或未取代的取代的芳基或未取代或取代的芳烷基，并且R 3是氢，烷基或环烷基，当R3是氢时，R2不能是氢，与药学上可接受的无毒惰性稀释剂或载体组合。

70. 发明授权

US4038406A 1,2,4-Triazole antimycotic compositions and use thereof 失效
标题翻译： 1,2,4-三唑抗菌组合物及其用途
公开(公告)号：US4038406A
公开(公告)日：1977-07-26
申请号：US645563
申请日：1975-12-31
申请人： Werner Meiser , Wolfgang Kramer , Karl Heinz Buchel , Manfred Plempel
发明人： Werner Meiser , Wolfgang Kramer , Karl Heinz Buchel , Manfred Plempel
IPC分类号： C07D249/08 , A61K31/41
CPC分类号： C07C45/63 , C07C45/004 , C07C45/70 , C07C45/71 , C07D249/08
摘要： Antimycotic compositions are produced which comprise an antimycotically effective amount of a 1,2,4-triazole of the formula: ##STR1## or a pharmaceutically acceptable non-toxic salt thereof wherein X.sup.1 is hydrogen or alkyl;X.sup.2 is hydrogen or alkyl;R.sup.1 is alkyl, unsubstituted or substituted aryl or unsubstituted or substituted aralkyl;R.sup.2 is hydrogen, alkyl or unsubstituted or substituted aryl;R.sup.3 is alkyl, cycloalkyl, unsubstituted or substituted aryl or unsubstituted or substituted aralkyl; andY is a keto group or a functional derivative of a keto group, in combination with a pharmaceutically acceptable non-toxic, inert diluent or carrier.

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