isocycloseram | 2061933-85-3

• 分子结构分类: 有机化合物 - 有机酸及其衍生物 - 羧酸及其衍生物
• 英文名称: isocycloseram
• 英文别名: Isocycloseram；4-[5-(3,5-dichloro-4-fluorophenyl)-5-(trifluoromethyl)-4H-1,2-oxazol-3-yl]-N-(2-ethyl-3-oxo-1,2-oxazolidin-4-yl)-2-methylbenzamide
• CAS: 2061933-85-3
• 化学式: C₂₃H₁₉Cl₂F₄N₃O₄
• 分子量: 548.321
• InChiKey: WLSQDEYDCAGPIR-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  5
• 重原子数：
  36
• 可旋转键数：
  5
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.35
• 拓扑面积：
  80.2
• 氢给体数：
  1
• 氢受体数：
  9

反应信息

• 作为产物：
  描述：

  4-(5-(3,5-dichloro-4-fluorophenyl)-5-(trifluoromethyl)-4,5-dihydroisoxazol-3-yl)-2-methylbenzoic acid 在 草酰氯 、 三乙胺 作用下， 以 二氯甲烷 、 乙酸乙酯 为溶剂， 反应 12.0h， 生成 isocycloseram
  参考文献：
  名称：

  [EN] ANTI-PARASITIC INFECTION EXTERNAL PHARMACEUTICAL FORMULATION, PREPARATION METHOD THEREFOR AND USE THEREOF
  [FR] FORMULATION PHARMACEUTIQUE EXTERNE ANTI-INFECTION PARASITAIRE, SON PROCÉDÉ DE PRÉPARATION ET SON UTILISATION
  [ZH] 一种抗寄生虫感染的外用药物制剂及其制备方法和应用

  摘要：

  一种抗寄生虫感染的外用药物制剂及其制备方法和应用，该外用药物制剂包括第一活性成分和醛类化合物，所述第一活性成分为异噁唑啉类化合物。所述药物制剂中的有效成分醛类化合物，该化合物不仅具有杀虫活性，还可以有效提高制剂的稳定性；并通过提高外用制剂的透皮速率，提高药物活性成分的利用率。

  公开号：

  WO2023221862A1

文献信息

• INSECTICIDAL COMPOUNDS BASED ON ISOAZOLINE DERIVATIVES
  申请人：Cassayre Jerome Yves

  公开号：US20120238517A1

  公开（公告）日：2012-09-20

  The present invention relates to compounds of formula (I): Wherein A 1 , A 2 , A 3 , A 4 , G 1 , L, Y 1 , Y 2 , Y 3 , Y 4 , R 1 , R 2 , R 3 and R 4 are as defined in claim 1 ; or a salt or N-oxide thereof. Furthermore, the present invention relates to intermediates for preparing compounds of formula (I), to compositions comprising them and to methods of using them to combat and control insect, acarine, nematode and mollusc pests.

  本发明涉及式(I)的化合物：其中A1、A2、A3、A4、G1、L、Y1、Y2、Y3、Y4、R1、R2、R3和R4如权利要求1所定义；或其盐或N-氧化物。此外，本发明涉及制备式(I)化合物的中间体，包含它们的组合物以及使用它们来对抗和控制昆虫、螨虫、线虫和软体动物害虫的方法。
• [EN] INSECTICIDAL COMPOUNDS BASED ON ISOXAZOLINE DERIVATIVES<br/>[FR] COMPOSÉS INSECTICIDES À BASE DE DÉRIVÉS ISOXAZOLINE
  申请人：SYNGENTA PARTICIPATIONS AG

  公开号：WO2011067272A1

  公开（公告）日：2011-06-09

  The present invention relates to compounds of formula (I): Wherein A1, A2, A3, A4, G1, L, Y1, Y2, Y3, Y4, R1, R2, R3 and R4 are as defined in claim 1; or a salt or N-oxide thereof. Furthermore, the present invention relates to intermediates for preparing compounds of formula (I), to compositions comprising them and to methods of using them to combat and control insect, acarine, nematode and mollusc pests.

  本发明涉及式(I)的化合物：其中A1、A2、A3、A4、G1、L、Y1、Y2、Y3、Y4、R1、R2、R3和R4如权利要求1所定义；或其盐或N-氧化物。此外，本发明涉及制备式(I)化合物的中间体，包含它们的组合物以及使用它们来对抗和控制昆虫、螨虫、线虫和软体动物害虫的方法。
• [EN] ISOXAZOLINE DERIVATIVES AS INSECTICIDAL COMPOUNDS<br/>[FR] DÉRIVÉS D'ISOXAZOLINE UTILISÉS COMME COMPOSÉS INSECTICIDES
  申请人：SYNGENTA PARTICIPATIONS AG

  公开号：WO2013050302A1

  公开（公告）日：2013-04-11

  The present invention provides compounds of formula I wherein G1 is oxygen; R1 is hydrogen; R2 is group P L is a bond, methylene or ethylene; R3 is hydrogen; R4 is independently hydrogen, cyano, cyano-C1-C8alkyl, C1-C8alkyl, C1-C8haloalkyl, C3-C8cycloalkyl, C3-C8cycloalkyl where one carbon atom is replaced by O, S, S(O) or SO2, or C3- Cgcycloalkyl-C1-C8alkyl, C3-C8cycloalkyl-C1-C8alkyl where one carbon atom in the cycloalkyl group is replaced by O, S, S(O) or SO2, or C3-C8cycloalkyl-C1-C8haloalkyl, C1-C8hydroxyalkyl, C1-C8alkoxy-C1-C8alkyl, C2-C8alkenyl, C2-C8haloalkenyl, C2-C8alkynyl, C2-C8haloalkynyl, phenyl, phenyl substituted by one to three R6, phenyl-C1-C4alkyl, phenyl-C1-C4alkyl wherein the phenyl moiety is substituted by one to three R6, 5-6 membered heteroaryl-C1-C4alkyl or 5-6 membered heteroaryl-C1-C4alkyl wherein the heteroaryl moiety is substituted by one to three R6, or C1-C4alkyl-(C1-C4alkyl-O-N=)C-CH2-; each R6 is independently halogen, cyano, nitro, C1-C8alkyl, C1-C8haloalkyl, C1-C8alkoxy, or C1- C8haloalkoxy; Y1, Y2 and Y3 are independently CH or nitrogen; wherein no more than two of Y1, Y2 and Y3 are nitrogen and wherein Y2 and Y3 are not both nitrogen; R5 is hydrogen, halogen, cyano, nitro, NH2, C1-C2alkyl, C1-C2haloalkyl, C3-C5cycloalkyl, C1- C2halocycloalkyl, C1-C2alkoxy, C1-C2haloalkoxy; or Y1 is CR7, and R5 and R7 together form a - CH=CH-CH=CH- bridge or a -N=CH-CH=CH- bridge; X2 is C-X6 or nitrogen; X1,X3 and X6 are independently hydrogen, halogen or trihalomethyl, wherein at least two of X1, X3 and X6 are not hydrogen; X4 is trifluoromethyl, difhioromethyl or chlorodifluoromethyl. or a salt or N-oxide thereof. The invention also provides intermediates useful for the preparation of compounds of formula I, as well as methods of controlling insects, acarines, nematodes or molluscs using the compounds of formula I.

  本发明提供了以下式I的化合物，其中G1是氧；R1是氢；R2是P基团；L是键，亚甲基或乙烯基；R3是氢；R4独立地是氢、氰基、氰基-C1-C8烷基、C1-C8烷基、C1-C8卤代烷基、C3-C8环烷基、C3-C8环烷基其中一个碳原子被O、S、S(O)或SO2取代，或C3-C8环烷基-C1-C8烷基、C3-C8环烷基-C1-C8烷基其中环烷基中一个碳原子被O、S、S(O)或SO2取代，或C3-C8环烷基-C1-C8卤代烷基、C1-C8羟基烷基、C1-C8烷氧基-C1-C8烷基、C2-C8烯基、C2-C8卤代烯基、C2-C8炔基、C2-C8卤代炔基、苯基、苯基取代一个至三个R6、苯基-C1-C4烷基、苯基-C1-C4烷基其中苯基取代一个至三个R6、5-6成员杂环烷基-C1-C4烷基或5-6成员杂环烷基-C1-C4烷基其中杂环烷基取代一个至三个R6，或C1-C4烷基-(C1-C4烷氧基-N=)C-CH2-；每个R6是独立的卤素、氰基、硝基、C1-C8烷基、C1-C8卤代烷基、C1-C8烷氧基或C1-C8卤代烷氧基；Y1、Y2和Y3独立地是CH或氮；其中不超过两个Y1、Y2和Y3是氮，且Y2和Y3不同时是氮；R5是氢、卤素、氰基、硝基、NH2、C1-C2烷基、C1-C2卤代烷基、C3-C5环烷基、C1-C2卤代环烷基、C1-C2烷氧基、C1-C2卤代烷氧基；或Y1是CR7，且R5和R7一起形成一个-CH=CH-CH=CH-桥或一个-N=CH-CH=CH-桥；X2是C-X6或氮；X1、X3和X6独立地是氢、卤素或三卤甲基，其中至少两个X1、X3和X6不是氢；X4是三氟甲基、二氟甲基或氯二氟甲基，或其盐或N-氧化物。本发明还提供了用于制备式I化合物的中间体，以及使用式I化合物控制昆虫、螨虫、线虫或软体动物的方法。
• Substituted Oxadiazoles for Combating Phytopathogenic Fungi
  申请人：BASF SE

  公开号：US20200045974A1

  公开（公告）日：2020-02-13

  The present invention relates to novel trifluoromethyloxadiazoles of the formula I, or the N-oxides, or the agriculturally useful salts thereof; and to their use for controlling phytopathogenic fungi; and to a method for combating phytopathogenic harmful fungi, which process comprises treating the fungi, the plants, the soil or seeds to be protected against fungal attack, with an effective amount of at least one compound of the formula I, or an N-oxide, or an agriculturally acceptable salt thereof; and to agrochemical compositions comprising at least one compound of the formula I; and to agrochemical compositions further comprising seeds.

  本发明涉及公式I的新型三氟甲氧噻二唑，或其N-氧化物，或其农业上有用的盐；以及它们用于控制植物病原真菌的用途；以及一种用于防治植物病原真菌的方法，该方法包括使用公式I的至少一种化合物，或其N-氧化物，或其农业上可接受的盐的有效量来处理真菌、植物、土壤或需要受到真菌攻击保护的种子；以及包含至少一种公式I的农药组合物；以及进一步包含种子的农药组合物。
• [EN] PROCESS FOR THE PREPARATION OF OPTICALLY ACTIVE ISOXAZOLINE COMPOUNDS<br/>[FR] PROCÉDÉ DE PRÉPARATION DE COMPOSÉS ISOXAZOLINE OPTIQUEMENT ACTIFS
  申请人：SYNGENTA PARTICIPATIONS AG

  公开号：WO2016023787A1

  公开（公告）日：2016-02-18

  The present invention relates to a process for the preparation of a compound of formula (I) wherein A1 and A2 are C-H, or one of A1 and A2 is C-H and the other is N; R1 is C1-C4alkyl, C1-C4haloalkyl or C3-C6cycloalkyl; each R2 is independently bromo, chloro, fluoro or trifluoromethyl; R3 is hydrogen; R4 is hydrogen, halogen, methyl, halomethyl or cyano; or R3 and R4 together form a bridging 1,3-butadiene group; R5 is chlorodifluoromethyl or trifluoromethyl; n is 2 or 3; by reacting a compound of formula (II) wherein A1, A2, R1, R2, R3, R4, R5 and n is as defined under formula (I) above, with hydroxylamine, a base and a chiral catalyst, characterized in that the chiral catalyst is a dimeric chiral catalyst of formula (III) wherein R6, R7, R8, R9, R10 and X are as defined in claim 1.

  本发明涉及一种制备式（I）化合物的方法，其中A1和A2是C-H，或者A1和A2中的一个是C-H，另一个是N；R1是C1-C4烷基，C1-C4卤代烷基或C3-C6环烷基；每个R2独立地是溴、氯、氟或三氟甲基；R3是氢；R4是氢、卤素、甲基、卤代甲基或氰基；或者R3和R4一起形成桥接的1,3-丁二烯基团；R5是氯二氟甲基或三氟甲基；n为2或3；通过将式（II）化合物与羟胺、碱和手性催化剂反应，其中A1、A2、R1、R2、R3、R4、R5和n如上述式（I）所定义，其特征在于手性催化剂是式（III）的二聚手性催化剂，其中R6、R7、R8、R9、R10和X如权利要求1所定义。