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1. 发明授权

US4151290A Fungicidal 1-cycloalkylcarbonyl-3-(3,5-dihalophenyl)imidazolidine-2,4-diones 失效
标题翻译：杀真菌剂1-环烷基羰基-3-（3,5-二卤苯基）咪唑烷-2,4-二酮
公开(公告)号：US4151290A
公开(公告)日：1979-04-24
申请号：US851899
申请日：1977-11-16
申请人： Chiyozo Takayama , Toshiro Kato , Shigeo Yamamoto , Yoshio Hisada , Nobuyuki Kameda , Akira Fujinami
发明人： Chiyozo Takayama , Toshiro Kato , Shigeo Yamamoto , Yoshio Hisada , Nobuyuki Kameda , Akira Fujinami
IPC分类号： A01N47/38 , A01N43/50 , A01N53/00 , A01N53/04 , A01P3/00 , C07D233/80 , A61K31/415
CPC分类号： C07D233/80 , A01N43/50 , A01N53/00
摘要： 1-Cycloalkylcarbonyl-3-(3,5-dihalophenyl)imidazolidine-2,4-diones of the formula: ##STR1## wherein X is a chlorine or bromine atom, R.sub.1 is a C.sub.3 -C.sub.6 cycloalkyl, tetramethylcyclopropyl, 2,2-dimethyl-3-isobutenylcyclopropyl or 2,2-dimethyl-3-dichlorovinylcyclopropyl group and R.sub.2 and R.sub.3 are individually a hydrogen atom or a methyl group, which show high fungicidal activities without any material toxicity to mammals and plants and which can be produced by reacting the corresponding 1-unsubstituted compound with a cycloalkanecarboxylic acid or a reactive derivative thereof.
摘要翻译：下式的1-环烷基羰基-3-（3,5-二卤苯基）咪唑烷-2,4-二酮其中X是氯或溴原子，R 1是C 3 -C 6环烷基，四甲基环丙基，二甲基-3-异丁烯基环丙基或2,2-二甲基-3-二氯乙烯基环丙基，R2和R3分别为氢原子或甲基，它们对哺乳动物和植物没有任何物质毒性，具有高杀真菌活性，可以通过使相应的1-未取代的化合物与环烷烃羧酸或其活性衍生物。

2. 发明授权

US4123549A N-(3,5-dihalophenyl)-.alpha.-spirocycloalkanesuccinimides, and their preparation and use 失效
标题翻译： N-（3,5-二卤代苯基） - {60-螺环烷基琥珀酰亚胺及其制备和用途
公开(公告)号：US4123549A
公开(公告)日：1978-10-31
申请号：US859756
申请日：1977-12-12
申请人： Nobuyuki Kameda , Yoshio Hisada , Chiyozo Takayama , Toshiro Kato , Akira Fujinami
发明人： Nobuyuki Kameda , Yoshio Hisada , Chiyozo Takayama , Toshiro Kato , Akira Fujinami
IPC分类号： A01N37/32 , A01P3/00 , C07D207/40 , C07D209/54 , A61K31/40
CPC分类号： C07D209/54 , A01N37/32
摘要： N-(3,5-Dihalophenyl)-.alpha.-spirocycloalkanesuccinimides of the formula: ##STR1## wherein X is a chlorine or bromine atom and R is a C.sub.3 -C.sub.6 alkylene group, which show high fungicidal activities without any material toxicity to mammals and plants and which can be produced by reacting the corresponding .alpha.-spirocycloalkanesuccinic acid or its anhydride with 3,5-dichloroaniline or 3,5-dibromoaniline.
摘要翻译： N-（3,5-二卤代苯基）-α-螺环烷基琥珀酰亚胺，其结构式如下：其中X为氯或溴原子，R为C3-C6亚烷基，对哺乳动物没有任何物质毒性，具有高杀真菌活性，植物，并且可以通过使相应的α-螺环烷基琥珀酸或其酸酐与3,5-二氯苯胺或3,5-二溴苯胺反应来制备。

3. 发明授权

US4110462A N'-Sulfenyl-N"-dihalophenylimidazolidinediones 失效
标题翻译： N“-SULFENYL-N” - 二氢壬基咪唑啉衍生物
公开(公告)号：US4110462A
公开(公告)日：1978-08-29
申请号：US747109
申请日：1976-12-03
申请人： Chiyozo Takayama , Shigeo Yamamoto , Toshiro Kato , Yoshio Hisada , Akira Fujinami
发明人： Chiyozo Takayama , Shigeo Yamamoto , Toshiro Kato , Yoshio Hisada , Akira Fujinami
IPC分类号： A01N47/04 , A01N43/50 , C07D233/80 , A01N9/12
CPC分类号： C07D233/80
摘要： 3-(3',5'-Dihalophenyl)-1-sulfenylimidazolidine-2,4-diones of the formula: ##STR1## wherein X is a chlorine atom or a bromine atom, Y.sub.1, Y.sub.2 and Y.sub.3 are each a chlorine atom or a fluorine atom and R.sub.1 and R.sub.2 are individually a hydrogen atom or a methyl group, which show high microbicidal activities against various fungi without any material toxicity to mammals and plants and can be produced by reacting the corresponding 1-unsubstituted compound with a sulfenyl halide.

4. 发明授权

US4056622A N-sulfonyl-N-dihalophenylimidazolidinediones 失效
标题翻译： N-磺酰基-N-二卤苯基咪唑烷二酮
公开(公告)号：US4056622A
公开(公告)日：1977-11-01
申请号：US677440
申请日：1976-04-15
申请人： Chiyozo Takayama , Yoshio Hisada , Toshiro Kato , Akira Fujinami
发明人： Chiyozo Takayama , Yoshio Hisada , Toshiro Kato , Akira Fujinami
IPC分类号： A01N43/50 , C07D233/80 , C07D233/86 , A61K31/415
CPC分类号： C07D233/80
摘要： 3-(3' -Dihalophenyl)-1-sulfonylimidazolidine-2,4-5'-diones of the formula: ##STR1## wherein X is a halogen atom, R.sub.1 is a C.sub.1 -C.sub.12 alkyl group, a C.sub.2 -C.sub.4 alkenyl group or a halogenated C.sub.1 -C.sub.4 alkyl group having 1 to 3 halogen atoms, and R.sub.2 and R.sub.3 are individually a hydrogen atom or a methyl group, which show high microbicidal activities against various fungi and bacteria without any material toxicity to mammals and which plants and can be produced by reacting the corresponding 1-unsubstituted compound with a sulfonyl halide.
摘要翻译：具有下式的3-（3'-二卤代苯基）-1-磺酰基咪唑烷-2,4-5'-二酮其中X是卤素原子，R 1是C 1 -C 12烷基，C 2 -C 4烯基或具有1至3个卤素原子的卤代C 1 -C 4烷基，R 2和R 3分别为氢原子或甲基，其对各种真菌和细菌具有高杀微生物活性，对哺乳动物无任何物质毒性，哪些植物和可植物通过使相应的1-未取代的化合物与磺酰卤反应来制备。

5. 发明授权

US4181732A 1-Branched-alkylcarbonyl-3-(3,5-dihalophenyl)imidazolidine-2,4-diones 失效
标题翻译： 1-支链烷基羰基-3-（3,5-二卤代苯基）咪唑烷-2,4-二酮
公开(公告)号：US4181732A
公开(公告)日：1980-01-01
申请号：US926396
申请日：1978-07-20
申请人： Chiyozo Takayama , Shigeo Yamamoto , Toshiro Kato , Yoshio Hisada , Shuichiro Asao , Yoshinori Nakayama
发明人： Chiyozo Takayama , Shigeo Yamamoto , Toshiro Kato , Yoshio Hisada , Shuichiro Asao , Yoshinori Nakayama
IPC分类号： A01N43/50 , C07D233/72 , C07D233/80 , A61K31/415
CPC分类号： C07D233/80 , A01N43/50
摘要： 1-Branched-alkylcarbonyl-3-(3,5-dihalophenyl)imidazolidine-2,4-diones of the formula: ##STR1## wherein X is a chlorine or bromine atom and R is a C.sub.3 -C.sub.5 branched alkyl group, which show high fungicidal activities without any material toxicity to mammals and plants and which can be produced by reacting the corresponding 1-unsubstituted compound with a branched alkanecarboxylic acid or a reactive derivative thereof.
摘要翻译： 1-支链烷基羰基-3-（3,5-二卤代苯基）咪唑烷-2,4-二酮，其结构式如下：其中X为氯或溴原子，R为C 3 -C 5支链烷基，其显示高杀真菌活性，对哺乳动物和植物没有任何物质毒性，可通过使相应的1-未取代的化合物与支链链烷羧酸或其活性衍生物反应来制备。

6. 发明授权

US4082849A Halogenated N-(3,5-dihalophenyl)cyclopropanedicarboximides 失效
标题翻译：羟基化N-（3,5-二羟基苯基）环丙烷二羧酸
公开(公告)号：US4082849A
公开(公告)日：1978-04-04
申请号：US730984
申请日：1976-10-08
申请人： Nobuyuki Kameda , Yoshio Hisada , Toshiro Kato , Akira Fujinami
发明人： Nobuyuki Kameda , Yoshio Hisada , Toshiro Kato , Akira Fujinami
IPC分类号： A01N53/00 , A01N37/32 , A01N53/12 , A01P1/00 , A01P3/00 , C07D209/52 , A61K31/40
CPC分类号： C07D209/52
摘要： Novel N-(3,5-dihalophenyl)cyclopropanedicarboximides of the formula: ##STR1## wherein X and Y are each a chlorine atom or a bromine atom and R.sub.1, R.sub.2 and R.sub.3 are individually a hydrogen atom or a methyl group, which show high microbicidal activities against various fungi and bacteria without any material toxicity to mammals and plants and which can be produced by reacting the corresponding cyclopropanedicarboxylic acid or its anhydride with a 3,5-dihaloaniline.

7. 发明授权

US4054668A N-substituted amino acid derivatives 失效
标题翻译： N-取代氨基酸衍生物
公开(公告)号：US4054668A
公开(公告)日：1977-10-18
申请号：US619125
申请日：1975-10-02
申请人： Osamu Kirino , Tadashi Ooishi , Nobuyuki Kameda , Toshiro Kato , Akira Fujinami , Toshiaki Ozaki
发明人： Osamu Kirino , Tadashi Ooishi , Nobuyuki Kameda , Toshiro Kato , Akira Fujinami , Toshiaki Ozaki
IPC分类号： A01N37/44 , C07C101/28 , A01N9/24 , A01N9/30 , C07C103/48
CPC分类号： A01N37/44
摘要： Novel N-substituted amino acid derivatives of the formula: ##STR1## wherein R.sub.1 is an alkenyl group having 2 to 5 carbon atoms, a halogen-substituted alkenyl group having 2 to 5 carbon atoms or an alkynyl group having 2 to 5 carbon atoms, R.sub.2 is a methyl or ##STR2## group in which R.sub.2 ' is an alkyl group having 1 to 4 carbon atoms or a halogen-substituted alkyl group having 1 to 4 carbon atoms; and R.sub.3 is a hydrogen atom, an alkyl having 1 to 20 carbon atoms, cycloalkyl having 3 to 6 carbon atoms, benzyl, hydroxyethyl or methoxyethyl group, and inorganic or organic acid addition salts thereof, which possess useful soil fungicidal activities and can be produced by reacting a sarcosine derivative of the formula:CH.sub.3 HNCH.sub.2 COOR.sub.3 (II)wherein R.sub.3 is as defined above, with a halogen compound of the formula:R.sub.1 -- X (III)wherein R.sub.1 is as defined above and X is a halogen atom, or by reacting an N-substituted glycine derivative of the formula: ##STR3## wherein R.sub.1 and R.sub.3 are as defined above, with an acyl compound of the formula: ##STR4## wherein R.sub.2 ' is as defined above and X is a halogen atom.
摘要翻译：式（I）的新型N-取代氨基酸衍生物：其中R 1是具有2至5个碳原子的烯基，具有2至5个碳原子的卤素取代的烯基或具有2至5个炔基的新的N-取代的氨基酸衍生物碳原子，R2是甲基或者基团，其中R2'是具有1至4个碳原子的烷基或具有1至4个碳原子的卤素取代的烷基; R3为氢原子，碳原子数1〜20的烷基，碳原子数为3〜6的环烷基，苄基，羟乙基或甲氧基乙基，以及无机或有机酸加成盐，具有有效的土壤杀真菌活性，通过使下式的肌氨酸衍生物：

8. 发明授权

US4025651A N-substituted-aminoacetamides used as fungicides 失效
标题翻译：用作杀真菌剂的N-取代 - 氨基乙酰胺
公开(公告)号：US4025651A
公开(公告)日：1977-05-24
申请号：US558604
申请日：1975-03-14
申请人： Osamu Kirino , Tadashi Ooishi , Nobuyuki Kameda , Toshiro Kato , Toshiaki Ozaki , Akira Fujinami
发明人： Osamu Kirino , Tadashi Ooishi , Nobuyuki Kameda , Toshiro Kato , Toshiaki Ozaki , Akira Fujinami
IPC分类号： C08K5/00 , A01N37/44 , A61K8/00 , A61K8/42 , A61Q17/00 , B27K3/36 , C07C67/00 , C07C231/00 , C07C231/02 , C07C231/06 , C07C237/06 , C08K5/20 , C08L1/00 , C08L7/00 , C08L21/00 , C08L27/00 , C08L77/00 , C09D7/00 , C09D7/12 , A01N9/20
CPC分类号： A01N37/44
摘要： N-substituted-aminoacetamide compounds having the formula (I) ##STR1## wherein R.sub.1 represents a lower alkenyl group having up to 5 carbon atoms, a halogen-substituted lower alkenyl group having up to 5 carbon atoms or a lower alkynyl group having up to 5 carbon atoms, R.sub.2 and R.sub.3, which may be the same or different, each represents a hydrogen atom or a lower akyl group having up to 4 carbon atoms, and the inorganic and organic acid addition salts thereof, which are useful as fungicidal agents, processesfor preparing N-substituted-aminoacetamide compounds and fungicidal compositions containing at least one compound of the formula (I) as an active inredient.
摘要翻译：具有式（I）的N-取代 - 氨基乙酰胺化合物其中R 1表示具有至多5个碳原子的低级烯基，具有至多5个碳原子的卤素取代的低级链烯基或低级炔基具有至多5个碳原子，可以相同或不同的R 2和R 3各自表示氢原子或具有至多4个碳原子的低级烷基，及其无机和有机酸加成盐，其可用作杀真菌剂，制备N-取代 - 氨基乙酰胺化合物的方法和含有至少一种式（I）化合物作为活性成分的杀真菌组合物。

9. 发明授权

US3966789A N-substituted aminonitrile derivatives 失效
标题翻译： N-取代氨基腈衍生物
公开(公告)号：US3966789A
公开(公告)日：1976-06-29
申请号：US503425
申请日：1974-09-05
申请人： Tadashi Oishi , Nobuyuki Kameda , Toshiro Kato , Akira Fujinami , Toshiaki Ozaki , Eiyashi Itooka
发明人： Tadashi Oishi , Nobuyuki Kameda , Toshiro Kato , Akira Fujinami , Toshiaki Ozaki , Eiyashi Itooka
IPC分类号： A01N37/34 , A01N20060101 , C02F1/50 , C07C20060101 , C07C67/00 , C07C253/00 , C07C255/29 , C07C121/417
摘要： N-substituted aminonitrile derivatives of the formula (I) ##EQU1## wherein R.sub.1, R.sub.2, R.sub.3 and R.sub.4 are as hereinafter defined, useful as fungicides, method for their preparation, and fungicidal compositions containing the N-substituted aminonitrile derivatives of the formula (I).
摘要翻译：式（I）的N-取代的氨基腈衍生物OR2R3 PARALLEL || R1-CNC-CN（I）| R4其中R1，R2，R3和R4如下文所定义，可用作杀真菌剂，其制备方法和杀真菌组合物含有式（I）的N-取代的氨基腈衍生物。

10. 发明授权

US4666943A Fungicidal anilides 失效
标题翻译：杀真菌剂
公开(公告)号：US4666943A
公开(公告)日：1987-05-19
申请号：US514799
申请日：1983-07-19
申请人： Hiroshi Noguchi , Toshiro Kato , Junya Takahashi , Yukio Ishiguri , Shigeo Yamamoto , Naonori Hirata
发明人： Hiroshi Noguchi , Toshiro Kato , Junya Takahashi , Yukio Ishiguri , Shigeo Yamamoto , Naonori Hirata
IPC分类号： A01N37/18 , A01N37/08 , A01N37/22 , A01N37/24 , A01N37/32 , A01N37/34 , A01N37/36 , A01N37/40 , A01N37/46 , A01N39/02 , A01N39/04 , A01N43/24 , A01N47/34 , A01N53/00 , A01N53/04 , A01N53/12 , A01N57/30 , C07C67/00 , C07C231/00 , C07C231/02 , C07C233/02 , C07C233/07 , C07C233/08 , C07C233/09 , C07C233/11 , C07C233/12 , C07C233/15 , C07C233/25 , C07C233/27 , C07C233/28 , C07C233/29 , C07C233/43 , C07C233/46 , C07C233/55 , C07C233/58 , C07C233/65 , C07C235/24 , C07C235/56 , C07C237/06 , C07C239/00 , C07C251/48 , C07C253/00 , C07C255/27 , C07C255/44 , C07C255/60
CPC分类号： C07C255/00 , A01N37/22 , A01N37/24 , A01N37/34 , A01N37/40 , A01N39/04 , A01N53/00
摘要： Use of an anilide of the formula: ##STR1## as a fungicidal agent against phytophatogenic fungi, particularly their strains resistant to benzimidazole thiophanate fungicides and/or cyclic imide fungicides.
摘要翻译：使用下式的酰苯胺：作为杀真菌剂的植物致病真菌，特别是其对苯并咪唑硫氮菌素杀真菌剂和/或环状酰亚胺杀真菌剂有抗性的菌株。

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