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1. 发明授权

US5157043A Fungicidal N-pyridyl imides 失效
标题翻译：杀真菌N-吡啶酰亚胺
公开(公告)号：US5157043A
公开(公告)日：1992-10-20
申请号：US593598
申请日：1990-11-01
申请人： Don R. Baker , Charles Kezerian , Francis H. Walker , Keith H. Brownell
发明人： Don R. Baker , Charles Kezerian , Francis H. Walker , Keith H. Brownell
IPC分类号： A01N47/18 , C07D213/75
CPC分类号： C07D213/75 , A01N47/18
摘要： Novel fungicidal pyridyl carboximides having the general structural formula ##STR1## wherein R is C.sub.1 -C.sub.6 alkyl, preferably methyl;R.sub.1 is selected from the group consisting of halogen such as chlorine, fluorine and bromine, C.sub.1 -C.sub.3 alkoxy such as propoxyethoxy and methoxy, preferably methoxy, and C.sub.2 -C.sub.4 alkenyloxy;R.sub.2 is selected from the group consisting of hydrogen, C.sub.1 -C.sub.6 alkyl, C.sub.4 -C.sub.6 cycloalkyl, heterocyclic moieties, aryl, preferably phenyl, substituted aryl, preferably substituted phenyl wherein the substitutions are chlorine, fluorine, bromine, trifluoromethyl and --NO.sub.3 ;X is --O or --S; andY is --O or --S;and fungicidally acceptable organic and inorganic salts thereof which are highly effective fungicides for use both as preventive and curative fungicides are disclosed herein.
摘要翻译：具有通式结构式（IMAGE）的新型杀真菌性吡啶基亚甲酰亚胺，其中R为C1-C6烷基，优选甲基; R 1选自卤素如氯，氟和溴，C 1 -C 3烷氧基如丙氧基乙氧基和甲氧基，优选甲氧基，和C 2 -C 4链烯氧基; R 2选自氢，C 1 -C 6烷基，C 4 -C 6环烷基，杂环部分，芳基，优选苯基，取代的芳基，优选取代的苯基，其中取代是氯，氟，溴，三氟甲基和-NO 3; X为-O或-S; 且Y为-O或-S; 并且这里公开了作为预防和治疗性杀真菌剂的高效杀真菌剂的杀真菌可接受的有机和无机盐。

2. 发明授权

US4914115A Fungicidal pyridyl cyclopropane carboximides 失效
标题翻译：杀真菌性吡啶环丙烷甲脒
公开(公告)号：US4914115A
公开(公告)日：1990-04-03
申请号：US193620
申请日：1988-05-13
申请人： Don R. Baker , Charles Kezerian , Keith H. Brownell
发明人： Don R. Baker , Charles Kezerian , Keith H. Brownell
IPC分类号： A01N53/00 , A01N53/04 , C07D213/75 , C07D213/76 , C07D405/12 , C07F7/10
CPC分类号： C07D213/75 , A01N53/00 , C07D213/76 , C07D405/12 , C07F7/10
摘要： Novel fungicidal pyridyl cyclopropane carboxamides having the general structural formula ##STR1## wherein R is selected from the group consisting of cycloalkyl, preferably cyclopropyl, hydrogen, alkyl, haloalkyl, substituted alkyl, aryl, substituted aryl, heteroalkyl, alkenyl, OR.sub.1, SR.sub.1 and ##STR2## wherein n is 0-10, preferably 0-2, and R.sub.1 is C.sub.1 -C.sub.4 alkyl, and R.sub.2 is selected from the group consisting of halogen such as chlorine, fluorine and bromine, preferably chlorine, C.sub.1 -C.sub.3 alkoxy such as propoxyethoxy and methoxy, preferably methoxy and C.sub.1 -C.sub.3 haloalkoxy, R.sub.3 is selected from the group consisting of hydrogen and methyl, X is --O or --S and Y is --O or --S; and fungicidally acceptable organic and inorganic salts thereof which are highly effective fungicides for use both as preventive and curative fungicides are disclosed herein.
摘要翻译：具有一般结构式的新型杀真菌吡啶环丙烷甲酰胺，其中R选自环烷基，优选环丙基，氢，烷基，卤代烷基，取代的烷基，芳基，取代的芳基，杂烷基，烯基，OR1，SR1和其中n为0-10，优选为0-2，并且R 1为C 1 -C 4烷基，R 2选自卤素如氯，氟和溴，优选氯，C 1 -C 3烷氧基如丙氧基乙氧基和甲氧基，优选甲氧基和C 1 -C 3卤代烷氧基，R 3选自氢和甲基，X是-O或-S，Y是-O或-S; 并且这里公开了作为预防和治疗性杀真菌剂的高效杀真菌剂的杀真菌可接受的有机和无机盐。

3. 发明授权

US4880831A Fungicidal carbanilates 失效
标题翻译：杀真菌剂
公开(公告)号：US4880831A
公开(公告)日：1989-11-14
申请号：US227037
申请日：1988-08-01
申请人： Don R. Baker , Keith H. Brownell , Charles Kezerian
发明人： Don R. Baker , Keith H. Brownell , Charles Kezerian
IPC分类号： A01N47/20
CPC分类号： A01N47/20
摘要： Novel fungicidal carbanilates having the general structural formula ##STR1## wherein R is methoxy or allyloxy; R.sub.1 is selected from the group consisting of hydrogen, C.sub.2 -C.sub.4 alkoxyalkyl and formyl; and R.sub.2 is C.sub.1 -C.sub.6 alkyl, preferably C.sub.2 -C.sub.3 alkyl which are highly effective fungicides are disclosed herein.
摘要翻译：新型的具有通式结构式（IMAGE）的杀真菌碳酸氢盐，其中R是甲氧基或烯丙氧基; R1选自氢，C 2 -C 4烷氧基烷基和甲酰基; 并且R 2是C 1 -C 6烷基，优选作为高效杀真菌剂的C 2 -C 3烷基。

4. 发明授权

US4797416A Fungicidal carbanilates 失效
标题翻译：杀真菌剂
公开(公告)号：US4797416A
公开(公告)日：1989-01-10
申请号：US607
申请日：1987-01-05
申请人： Don R. Baker , Keith H. Brownell , Charles Kezerian
发明人： Don R. Baker , Keith H. Brownell , Charles Kezerian
IPC分类号： A01N47/20 , C07C67/00 , C07C325/00 , C07C333/08 , C07C155/02 , A01N47/10
CPC分类号： A01N47/20
摘要： Novel fungicidal carbanilates having the general structural formula ##STR1## wherein R is methoxy or allyloxy; R.sub.1 is selected from the group consisting of hydrogen, C.sub.2 -C.sub.4 alkoxyalkyl and formyl; and R.sub.2 is C.sub.1 -C.sub.6 alkyl, preferably C.sub.2 -C.sub.3 alkyl which are highly effective fungicides are disclosed herein.

5. 发明授权

US4767772A Fungicidal pyridyl cyclopropane carboximides 失效
标题翻译：杀真菌性吡啶环丙烷甲脒
公开(公告)号：US4767772A
公开(公告)日：1988-08-30
申请号：US36545
申请日：1987-04-15
申请人： Don R. Baker , Charles Kezerian , Keith H. Brownell
发明人： Don R. Baker , Charles Kezerian , Keith H. Brownell
IPC分类号： A01N53/00 , A01N53/12 , C07D213/75 , C07D213/76 , C07D405/12 , C07F7/10 , A01N43/40
CPC分类号： C07D213/75 , A01N53/00 , C07D213/76 , C07D405/12 , C07F7/10
摘要： Novel fungicidal pyridyl cyclopropane carboxamides having the general structural formula ##STR1## wherein R is selected from the group consisting of cycloalkyl, preferably cyclopropyl, hydrogen, alkyl, haloalkyl, substituted alkyl, aryl, substituted aryl, heteroalkyl, alkenyl, OR.sub.1, SR.sub.1 and ##STR2## wherein n is 0-10, preferably 0-2, and R.sub.1 is C.sub.1 -R.sub.4 alkyl, and R.sub.2 is selected from the group consisting of halogen such as chlorine, fluorine and bromine, preferably chlorine, C.sub.1 -C.sub.3 alkoxy such as propoxyethoxy and methoxy, preferably methoxy and C.sub.1 -C.sub.3 haloalkoxy, R.sub.3 is selected from the group consisting of hydrogen and methyl, X is --O or --S and Y is --O or --S; and fungicidally acceptable organic and inorganic salts thereof which are highly effective fungicides for use both as preventive and curative fungicides are disclosed herein.
摘要翻译：具有通式结构式的新型杀真菌吡啶环丙烷甲酰胺，其中R选自环烷基，优选环丙基，氢，烷基，卤代烷基，取代的烷基，芳基，取代的芳基，杂烷基，链烯基，OR1，SR1和其中n为0-10，优选为0-2，R 1为C 1〜R 4烷基，R 2选自卤素如氯，氟和溴，优选氯，C 1 -C 3烷氧基如丙氧基乙氧基和甲氧基，优选甲氧基和C 1 -C 3卤代烷氧基，R 3选自氢和甲基，X是-O或-S，Y是-O或-S; 并且这里公开了作为预防和治疗性杀真菌剂的高效杀真菌剂的杀真菌可接受的有机和无机盐。

6. 发明授权

US4931451A Fungicidal pyridyl sulfenyl carbamates 失效
标题翻译：杀真菌的吡啶基亚磺酰基氨基甲酸酯
公开(公告)号：US4931451A
公开(公告)日：1990-06-05
申请号：US258409
申请日：1988-10-17
申请人： Don R. Baker , Francis H. Walker , Keith H. Brownell
发明人： Don R. Baker , Francis H. Walker , Keith H. Brownell
IPC分类号： A01N47/24 , C07D213/76
CPC分类号： C07D213/76 , A01N47/24
摘要： Novel fungicidal pyridyl sulfenyl carbamates having the formula ##STR1## wherein R is selected from the group consisting of haloalkyl, C.sub.1 -C.sub.8 alkyl, aryl, substituted aryl, arylalkyl, substituted arylalkyl, alkanoyl, alkylamino, arylamino, arylalkylamino and substituted pyridylcarbamoyl;R.sub.1 is C.sub.1 -C.sub.3 alkoxy or C.sub.1 -C.sub.3 haloalkoxy or halomethoxy; alkenyloxy; and halogen;R.sub.2 is C.sub.1 -C.sub.3 alkyl;X is oxygen or sulfur; andY is oxygen or sulfurand fungicidally acceptable organic and inorganic salts thereof which are highly effective fungicides for use both as preventive and curative fungicides are disclosed herein.
摘要翻译：具有下式的新型杀真菌吡啶基硫基氨基甲酸酯：其中R选自卤代烷基，C 1 -C 8烷基，芳基，取代的芳基，芳基烷基，取代的芳基烷基，烷酰基，烷基氨基，芳基氨基，芳基烷基氨基和取代的吡啶基氨基甲酰基; R1是C1-C3烷氧基或C1-C3卤代烷氧基或卤代甲氧基; 链烯氧基和卤素; R2是C1-C3烷基; X是氧或硫; 并且Y是氧或硫，并且其杀真菌可接受的有机和无机盐是用作预防和治疗性杀真菌剂的高效杀真菌剂。

7. 发明授权

US4800205A Fungicidal pyridyl sulfenyl carbamates 失效
标题翻译：杀真菌的吡啶基亚磺酰基氨基甲酸酯
公开(公告)号：US4800205A
公开(公告)日：1989-01-24
申请号：US114811
申请日：1987-10-29
申请人： Don R. Baker , Francis H. Walker , Keith H. Brownell
发明人： Don R. Baker , Francis H. Walker , Keith H. Brownell
IPC分类号： A01N47/24 , C07D213/76 , C07D213/64 , A01N43/40 , C07D213/75
CPC分类号： C07D213/76 , A01N47/24
摘要： Novel fungicidal pyridyl sulfenyl carbamates having the formula ##STR1## wherein R is selected from the group consisting of haloalkyl, C.sub.1 -C.sub.8 alkyl, aryl, substituted aryl, arylalkyl, substituted arylalkyl, alkanoyl, alkylamino, arylamino, arylalkylamino and substituted pyridylcarbamoyl;R.sub.1 is C.sub.1 -C.sub.3 alkoxy or C.sub.1 -C.sub.3 haloalkoxy or halomethoxy; alkenyloxy; and halogen;R.sub.2 is C.sub.1 -C.sub.3 alkyl;X is oxygen or sulfur; andY is oxygen or sulfurand fungicidally acceptable organic and inorganic salts thereof which are highly effective fungicides for use both as preventive and curative fungicides are disclosed herein.

8. 发明授权

US4977164A Fungicidal N-(substituted thio)-pyridyl cyclopropane carboxamides 失效
标题翻译：杀真菌剂N-（取代硫代） - 吡啶基环丙烷甲酰胺
公开(公告)号：US4977164A
公开(公告)日：1990-12-11
申请号：US250477
申请日：1988-09-28
申请人： Don R. Baker , Keith H. Brownell
发明人： Don R. Baker , Keith H. Brownell
IPC分类号： A01N53/00 , A01N53/04 , C07D213/75 , C07D213/76 , C07D405/12 , C07F7/10
CPC分类号： C07D213/76 , A01N53/00 , C07D213/75 , C07D405/12 , C07F7/10
摘要： Novel fungicidal pyridyl cyclopropane carboxamides having the general structural formula ##STR1## wherein R is selected from the group consisting of haloalkyl, preferably C.sub.1 -C.sub.3 haloalkyl, C.sub.1 -C.sub.8 alkyl, aryl, substituted aryl, and arylalkyl wherein the preferred aryl is phenyl, the alkyl is C.sub.1 -C.sub.3 alkyl and the preferred substitutions are Cl, Br, F and nitro, alkanoyl, preferably C.sub.1 -C.sub.4 alkanoyl, ##STR2## wherein R.sub.3 and R.sub.4 can be alkyl, alkanoyl, alkoxycarbanoyl, benzyl, pyridyl and substituted pyridyl, and when R.sub.3 and Rhd 4 are alkyl together with --N they can form a heterocyclic ring such as piperidine, R.sub.1 -C.sub.3 alkoxy or C.sub.1 -C.sub.3 haloalkoxy, preferably methoxy or halomethoxy and halogen wherein the halogen is chlorine, bromine or fluorine, R.sub.2 is hydrogen or methyl, and fungicidally acceptable organic and inorganic salts thereof which are highly effective fungicides for use both as preventive and curative fungicides are disclosed herein. These compounds provide excellent control of fungal growth.
摘要翻译：新颖的具有通式结构式为“IMAGE”的杀真菌吡啶环丙烷甲酰胺，其中R选自卤代烷基，优选C 1 -C 3卤代烷基，C 1 -C 8烷基，芳基，取代的芳基和芳基烷基，其中优选的芳基是苯基，烷基是C 1 -C 3烷基，优选的取代是Cl，Br，F和硝基，烷酰基，优选C 1 -C 4烷酰基，其中R 3和R 4可以是烷基，烷酰基，烷氧基羰基，苄基，吡啶基和取代的吡啶基，和当R3和Rhd4与-N一起烷基时，它们可以形成杂环，例如哌啶，R 1 -C 3烷氧基或C 1 -C 3卤代烷氧基，优选甲氧基或卤代甲氧基和卤素，其中卤素是氯，溴或氟，R 2是氢或甲基，以及作为预防和治疗性杀真菌剂的高效杀真菌剂的杀真菌可接受的有机和无机盐。这些化合物提供极好的真菌生长控制。

9. 发明授权

US4975443A Fungicidal pyridyl iminocarbonates 失效
标题翻译：杀真菌吡啶亚氨基碳酸盐
公开(公告)号：US4975443A
公开(公告)日：1990-12-04
申请号：US308583
申请日：1989-02-10
申请人： Don R. Baker , Keith H. Brownell
发明人： Don R. Baker , Keith H. Brownell
IPC分类号： A01N47/42 , C07D213/75
CPC分类号： C07D213/75 , A01N47/42
摘要： Novel fungicidal pyridyl iminocarbonates having the general structural formula ##STR1## wherein R is selected from the group consisting of C.sub.1 -C.sub.16 alkyl, C.sub.3 -C.sub.8 cycloalkyl, C.sub.2 -C.sub.8 alkenyl, C.sub.2 -C.sub.8 substituted alkenyl, C.sub.3 -C.sub.4 carboalkoxyalkyl, aryl, arylalkyl having C.sub.1 -C.sub.3 alkyl, substituted aryl and arylalkyl wherein the substituents are --Cl, --Br, --F and --NO.sub.2 ; furfuryl, pyridyl, C.sub.1 -C.sub.6 alkyl substituted phosphorus, alkanoyl, alkoxycarbonyl, aroyl, preferably benzoyl, alkylthioarbonyl, alkylthioalkyl, alkoxyalkyl, alkoxybenzyl and ##STR2## wherein R.sub.3 and R.sub.4 are C.sub.1 -C.sub.10 alkyl and can form a heterocyclic ring;R.sub.1 is selected from the group consisting of halogen, C.sub.1 -C.sub.3 alkoxy, C.sub.3 -C.sub.4 alkenyloxy and C.sub.1 -C.sub.3 haloalkoxy;R.sub.2 is selected from the group consisting of C.sub.1 -C.sub.4 alkyl;X is sulfur or oxygen;Y is sulfur or oxygen; andZ is sulfur or oxygen;and fungicidally acceptable organic and inorganic salts thereof which are highly effective fungicides for use both as preventive and curative fungicides are disclosed herein.
摘要翻译：新型的具有通式结构式为“IMAGE”的杀真菌吡啶基亚氨基碳酸酯，其中R选自C 1 -C 16烷基，C 3 -C 8环烷基，C 2 -C 8烯基，C 2 -C 8取代烯基，C 3 -C 4烷氧羰基烷基，芳基，芳烷基具有C 1 -C 3烷基，取代的芳基和芳烷基，其中取代基是-Cl，-Br，-F和-NO 2; 糠基，吡啶基，C1-C6烷基取代的磷，烷酰基，烷氧基羰基，芳酰基，优选苯甲酰基，烷硫基羰基，烷硫基烷基，烷氧基烷基，烷氧基苄基和其中R3和R4是C1-C10烷基并且可以形成杂环; R 1选自卤素，C 1 -C 3烷氧基，C 3 -C 4烯氧基和C 1 -C 3卤代烷氧基; R2选自C1-C4烷基; X是硫或氧; Y是硫或氧; Z为硫或氧; 并且这里公开了作为预防和治疗性杀真菌剂的高效杀真菌剂的杀真菌可接受的有机和无机盐。

10. 发明授权

US4975442A Fungicidal pyridyl cyclopropane carboxamidines 失效
公开(公告)号：US4975442A
公开(公告)日：1990-12-04
申请号：US308582
申请日：1989-02-10
申请人： Don R. Baker , Keith H. Brownell
发明人： Don R. Baker , Keith H. Brownell
IPC分类号： A01N53/00 , C07D213/75
CPC分类号： C07D213/75 , A01N53/00
摘要： Novel fungicidal pyridyl cyclopropane carboxamidines having the general structural formula ##STR1## and tautomers thereof whereinR is selected from the group consisting of hydrogen, pyridyl, substituted pyridyl, C.sub.1 -C.sub.3 alkoxy, C.sub.1 -C.sub.6 alkyl, acyl, carbamoyl, sulfonyl and cyano;R.sub.1 is selected from the group consisting of halogen, C.sub.1 -C.sub.3 alkoxy and C.sub.1 -C.sub.3 alkenyloxy;R.sub.2 is selected from the group consisting of hydrogen and C.sub.1 -C.sub.3 alkyl;R.sub.3 is selected from the group consisting of hydrogen, alkyl, aryl or arylalkyl;and fungicidally acceptable organic and inorganic salts thereof.

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