2-amino-3,5-dichloro-N-(diethyl-λ⁴-sulfanylidene)benzamide | 1422677-59-5

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: 2-amino-3,5-dichloro-N-(diethyl-λ⁴-sulfanylidene)benzamide
• 英文别名: 2-amino-3,5-dichloro-N-(diethyl-lambda4-sulfanylidene)benzamide；2-amino-3,5-dichloro-N-(diethyl-λ4-sulfanylidene)benzamide
• CAS: 1422677-59-5
• 化学式: C₁₁H₁₄Cl₂N₂OS
• 分子量: 293.217
• InChiKey: KYBRHFXMWNDJCL-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.5
• 重原子数：
  17
• 可旋转键数：
  3
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.36
• 拓扑面积：
  74.7
• 氢给体数：
  1
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  1-(3-chloro-2-pyridinyl)-3-trifluoromethyl-1H-pyrazole-5-carbonyl chloride 、 2-amino-3,5-dichloro-N-(diethyl-λ⁴-sulfanylidene)benzamide 在 吡啶 、 4-二甲氨基吡啶 作用下， 反应 1.0h， 以28%的产率得到2-(3-chloro-2-pyridyl)-N-[2,4-dichloro-6-[(diethyl-λ⁴-sulfanylidene)carbamoyl]phenyl]-5-(trifluoromethyl)-2H-pyrazole-3-carboxamide
  参考文献：
  名称：

  [EN] PROCESS FOR PREPARING N-SUBSTITUTED 1H-PYRAZOLE-5-CARBONYLCHLORIDE COMPOUNDS
  [FR] PROCÉDÉ DE PRÉPARATION DE COMPOSÉS 1H-PYRAZOLE-5-CARBONYLCHORURES N-SUBSTITUÉS

  摘要：

  本发明涉及一种制备式(I)N-取代1H-吡唑-5-羰基氯化物的过程，包括以下步骤：i) 用选择自碳或氮与锂结合的有机锂碱或碳与镁结合的有机镁碱的碱去质子化式(II)化合物；和ii) 将步骤(i)中获得的产物经氯羰基化反应，与磷酰氯或磷酰氯等效物中选择的试剂反应，以获得式(I)化合物。

  公开号：

  WO2013024007A1
• 作为产物：
  描述：

  3,5-二氯靛红酸酐 、 S,S-diethyl sulfinium sulfate 在 三乙胺 作用下， 以 二甲基亚砜 为溶剂， 反应 6.0h， 以94%的产率得到2-amino-3,5-dichloro-N-(diethyl-λ⁴-sulfanylidene)benzamide
  参考文献：
  名称：

  [EN] N-THIO-ANTHRANILAMIDE COMPOUNDS AND THEIR USE AS PESTICIDES
  [FR] COMPOSÉS N-THIO-ANTHRANILAMIDES ET LEUR UTILISATION COMME PESTICIDES

  摘要：

  本发明涉及公式（I）的N-硫代苯甲酰胺化合物，其立体异构体，盐，互变异构体和N-氧化物，其中R1是卤素或卤代甲基；R2是氢，卤素或氰基；R3是氢，C1-C4烷基，C1-C4卤代烷基，C2-C6-烯基或类似物；R4是卤素；R5和R6彼此独立地是可选择取代的C1-C6烷基，C3-C6环烷基，C2-C6烯基，C2-C6炔基，苯基，或者一起代表一个（杂）脂肪链，或类似物；k为0或1。本发明还涉及用于对抗或控制无脊椎动物害虫的方法，用于保护植物繁殖材料和/或由此生长的植物的方法，包括至少一种根据本发明的化合物的植物繁殖材料，用于治疗或保护动物免受寄生虫侵扰或感染的方法，用于制备用于治疗受感染动物和/或保护动物免受寄生虫侵扰或感染的组合物的方法，以及用于作为药物的本发明的化合物。

  公开号：

  WO2013024009A1

文献信息

• [EN] ANILINE TYPE COMPOUNDS<br/>[FR] COMPOSÉS DE TYPE ANILINES
  申请人：BASF SE

  公开号：WO2013024008A1

  公开（公告）日：2013-02-21

  The present invention relates to compounds of the formula (I) wherein R1 and R2 independently of one another are hydrogen, C1-C10-alkyl, C1-C10-haloalkyl, C3-C10-cycloalkyl, C3-C10-halocycloalkyl, C2-C10-alkenyl, C2-C10-haloalkenyl or together represent an aliphatic chain, or the like; R3 is halogen, cyano, C1-C8-alkyl, C1-C8- haloalkyl, C3-C8-cycloalkyl, C3-C8-halocycloalkyl, C2-C8-alkenyl, C2-C8-haloalkenyl, C1-C8-alkoxy, phenyl, or the like; R4 is hydrogen, C1-C10-alkyl, C1-C10-haloalkyl, C3-C8- cycloalkyl, C3-C8-halocycloalkyl, C2-C10-alkenyl, C2-C10-haloalkenyl, phenyl, or the like; t is 0 or 1; p is 0, 1, 2, 3 or 4. The present invention also relates to a process for preparing a compound of the formula (I) which comprises reacting a compound of the formula (II) with a compound of the formulae (III) or (IV): where t, p, R1 R3, R3 and R4 are as defined in any of claims 1 to 6 and where A- is an equivalent of an anion having a pΚB of at least 10 (determined under standard conditions in water).

  本发明涉及以下式(I)的化合物，其中R1和R2彼此独立地为氢、C1-C10-烷基、C1-C10-卤代烷基、C3-C10-环烷基、C3-C10-卤代环烷基、C2-C10-烯基、C2-C10-卤代烯基或者一起代表一个脂肪链等；R3为卤素、氰基、C1-C8-烷基、C1-C8-卤代烷基、C3-C8-环烷基、C3-C8-卤代环烷基、C2-C8-烯基、C2-C8-卤代烯基、C1-C8-烷氧基、苯基等；R4为氢、C1-C10-烷基、C1-C10-卤代烷基、C3-C8-环烷基、C3-C8-卤代环烷基、C2-C10-烯基、C2-C10-卤代烯基、苯基等；t为0或1；p为0、1、2、3或4。本发明还涉及一种制备上述式(I)化合物的方法，包括将式(II)的化合物与式(III)或(IV)的化合物反应：其中t、p、R1、R3、R3和R4如权利要求1至6中的任一所定义，A-是至少在水中标准条件下具有至少10的pΚB值的阴离子的当量。
• [EN] PROCESS FOR PREPARING N-SUBSTITUTED 1H-PYRAZOLE-5-CARBOXYLATE COMPOUNDS AND DERIVATIVES THEREOF<br/>[FR] PROCÉDÉ DE PRÉPARATION D'UN COMPOSÉ N-1 H-PYRAZOLE SUBSTITUÉ-5-CARBOXYLATE ET DE SES DÉRIVÉS
  申请人：BASF SE

  公开号：WO2013076092A1

  公开（公告）日：2013-05-30

  The present invention relates to a process for preparing an N-substituted 1 H-pyrazole- 5- carboxylate compound of the formula (l-A) comprising the steps of i) deprotonating a compound of the formula (II) in which the variables R1, R2 and r are each as defined in the description and the claims, with a magnesium-organic base having a carbon bound magnesium; and ii) subjecting the product obtained in step (i) to a carbonylation by reacting it with a reagent selected from the group consisting carbon dioxide or a carbon dioxide equivalent, to obtain a compound of formula (l-A); and it relates to further conversions to yield a N-substituted 1H-pyrazole-5-carbonyl chloride compound of the formula (I).

  本发明涉及一种制备式(l-A)的N-取代1 H-吡唑-5-羧酸酯化合物的过程，包括以下步骤：i) 用具有碳键镁的镁有机碱去质子化式(II)的化合物，其中变量R1、R2和r如描述和索赔中定义，并ii) 将步骤(i)中得到的产物经过羰基化反应，与选择自二氧化碳或二氧化碳等效物的试剂反应，得到式(l-A)的化合物；并且涉及进一步的转化以产生式(I)的N-取代1H-吡唑-5-羰基氯化物化合物。
• [EN] USE OF ANTHRANILAMIDE COMPOUNDS FOR REDUCING INSECT-VECTORED VIRAL INFECTIONS<br/>[FR] UTILISATION DE COMPOSÉS D'ANTHRANILAMIDES POUR RÉDUIRE LES INFECTIONS VIRALES VÉHICULÉES PAR LES INSECTES
  申请人：BASF SE

  公开号：WO2014079820A1

  公开（公告）日：2014-05-30

  The present invention relates to agricultural methods using anthranilamide compounds of formula (I) wherein R1, R2, R3, R4, R5, R6, R7 and k are as defined in the description; and their mixtures. The anthranilamide compounds of formula (I) are highly suitable for methods for reducing insect-vectored viral infection and transmission in plants, methods of reducing damage to plants caused by viral infection, and methods of crop enhancement including methods for improving plant growth, vigour and yield, by application of a combination of an anthranilic bis-amide or an aminothiadiazole (ryanodine receptor modulator) insecticide and a plant activator,to compositions comprising the combinations and to plant propagation material treated therewith.

  本发明涉及使用式(I)中R1、R2、R3、R4、R5、R6、R7和k如描述中定义的蒽酰胺化合物的农业方法；以及它们的混合物。式(I)中的蒽酰胺化合物非常适用于减少植物受昆虫传播的病毒感染和传播的方法，减少病毒感染引起的植物损害的方法，以及包括改善植物生长、活力和产量的作物增强方法，通过应用蒽酰双酰胺或氨基噻二唑（莱诺啶受体调节剂）杀虫剂和植物活化剂的组合，以及包含这些组合的组合物和经处理的植物繁殖材料。
• N-Thio-Anthranilamide Compounds and Their Use as Pesticides
  申请人：Kaiser Florian

  公开号：US20140155264A1

  公开（公告）日：2014-06-05

  The present invention relates to N-thio-anthranilamide compounds of the formula (I), the stereoisomers, the salts, the tautomers and the N-oxides thereof, wherein R 1 is halogen or halomethyl; R 2 is hydrogen, halogen or cyano; R 3 is hydrogen, C 1 -C 4 alkyl, C 1 -C 4 haloalkyl, C 2 -C 6 -alkenyl or the like; R 4 is halogen; R 5 and R 6 independently of each other are optionally substituted C 1 -C 6 -alkyl, C 3 -C 6 -cycloalkyl, C 2 -C 6 -alkenyl, C 2 -C 6 -alkynyl, phenyl, or together represent an (hetero)aliphatic chain, or the like; k is 0 or 1. The present invention further relates to a method for combating or controlling invertebrate pests, to a method for protecting plant propagation material and/or the plants which grow therefrom, to plant propagation material comprising at least one compound according to the present invention, to a method for treating or protecting an animal from infestation or infection by parasites, to a process for the preparation of a composition for treating infested or infected animals and/or for protecting animals against infestation or infection by parasites, and to a compound according to the invention for use as a medicament.

  本发明涉及公式（I）的N-硫基蒽酰胺化合物，其立体异构体，盐，互变异构体和N-氧化物，其中R1是卤素或卤甲基; R2是氢，卤素或氰基; R3是氢，C1-C4烷基，C1-C4卤代烷基，C2-C6烯基或类似物; R4是卤素; R5和R6独立地是可选的取代C1-C6烷基，C3-C6环烷基，C2-C6烯基，C2-C6炔基，苯基或共同表示（杂）脂肪链或类似物; k为0或1。本发明还涉及一种用于对抗或控制无脊椎动物害虫的方法，一种用于保护植物繁殖材料和/或从中生长的植物的方法，包括至少一种根据本发明的化合物的植物繁殖材料，一种用于治疗或保护动物免受寄生虫感染的方法，一种用于制备用于治疗受感染或感染动物和/或保护动物免受寄生虫感染的组合物的方法，以及用于作为药物的本发明化合物。
• Aniline Type Compounds
  申请人：Koerber Karsten

  公开号：US20140155451A1

  公开（公告）日：2014-06-05

  The present invention relates to compounds of the formula (I) wherein R 1 and R 2 independently of one another are hydrogen, C 1 -C 10 -alkyl, C 1 -C 10 -haloalkyl, C 3 -C 10 -cycloalkyl, C 3 -C 10 -halocycloalkyl, C 2 -C 10 -alkenyl, C 2 -C 10 -haloalkenyl or together represent an aliphatic chain, or the like; R 3 is halogen, cyano, C 1 -C 8 -alkyl, C 1 -C 8 -haloalkyl, C 3 -C 8 -cycloalkyl, C 3 -C 8 -halocycloalkyl, C 2 -C 8 -alkenyl, C 2 -C 8 -haloalkenyl, C 1 -C 8 -alkoxy, phenyl, or the like; R 4 is hydrogen, C 1 -C 10 -alkyl, C 1 -C 10 -haloalkyl, C 3 -C 8 -cycloalkyl, C 3 -C 8 -halocycloalkyl, C 2 -C 10 -alkenyl, C 2 -C 10 -haloalkenyl, phenyl, or the like; t is 0 or 1; p is 0, 1, 2, 3 or 4. The present invention also relates to a process for preparing a compound of the formula (I) which comprises reacting a compound of the formula II with a compound of the formulae III or IV: where t, p, R 1 R 3 , R 3 and R 4 are as defined in any of claims 1 to 6 and where A − is an equivalent of an anion having a pK B of at least 10 (determined under standard conditions in water).

  本发明涉及式(I)的化合物，其中R1和R2独立地是氢，C1-C10-烷基，C1-C10-卤代烷基，C3-C10-环烷基，C3-C10-卤代环烷基，C2-C10-烯基，C2-C10-卤代烯基或一起代表脂肪链等；R3是卤素，氰基，C1-C8-烷基，C1-C8-卤代烷基，C3-C8-环烷基，C3-C8-卤代环烷基，C2-C8-烯基，C2-C8-卤代烯基，C1-C8-烷氧基，苯基或类似物；R4是氢，C1-C10-烷基，C1-C10-卤代烷基，C3-C8-环烷基，C3-C8-卤代环烷基，C2-C10-烯基，C2-C10-卤代烯基，苯基或类似物；t为0或1；p为0、1、2、3或4。本发明还涉及一种制备式(I)化合物的方法，该方法包括将式II的化合物与式III或IV的化合物反应：其中t、p、R1、R3、R3和R4如权利要求1至6中的任何一项中所定义，A-是至少具有10的pKB（在水中标准条件下测定）的阴离子当量。