4-fluorophenylmethyl 4-amino-3-fluorophenyl ether | 154079-96-6

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯酚醚
• 英文名称: 4-fluorophenylmethyl 4-amino-3-fluorophenyl ether
• 英文别名: 2-Fluoro-4-(4-fluoro-benzyloxy)-phenylamine；2-Fluoro-4-(4-Fluoro-benzyloxy)-aniline；2-fluoro-4-[(4-fluorophenyl)methoxy]aniline
• CAS: 154079-96-6
• 化学式: C₁₃H₁₁F₂NO
• 分子量: 235.233
• InChiKey: DLWQXIMGMREALB-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3
• 重原子数：
  17
• 可旋转键数：
  3
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.08
• 拓扑面积：
  35.2
• 氢给体数：
  1
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  4-fluorophenylmethyl 4-amino-3-fluorophenyl ether 以95%的产率得到N-[2-fluoro-4-(4-fluoro-benzyloxy)-phenyl]-malonamic acid methyl ester
  参考文献：
  名称：

  N-acylamino benzyl ether derivatives

  摘要：

  这项发明涉及公式1的N-酰氨基芳基衍生物，其中R1、R21、R22、R23、R3、R4、R5、R6、R7、R8、R和n如本文所定义，且X为—CHRO、—OCHR—、—CH2S—、—SCH2—、—CH2CH2—、—CH═CH—或—C≡C—。该发明的化合物是选择性的单胺氧化酶B抑制剂，因此它们在治疗由单胺氧化酶B介导的疾病中具有用途，例如用于治疗阿尔茨海默病或老年性痴呆症。

  公开号：

  US20030232883A1
• 作为产物：
  描述：

  4-fluorophenylmethyl 3-fluoro-4-nitrophenyl ether 在 铁粉 乙酸乙酯 、 水 、 magnesium sulfate 、 二氯甲烷 作用下， 以 溶剂黄146 、 水 为溶剂， 以leaving 6.8 g of 4-fluorophenylmethyl 4-amino-3-fluorophenyl ether as a solid, m.p. 42°-43° C.的产率得到4-fluorophenylmethyl 4-amino-3-fluorophenyl ether
  参考文献：
  名称：

  Herbicical 2-[(4-heterocyclic-phenoxymethyl)phenoxy]-alkanoates

  摘要：

  本文揭示了杀草化合物、含有它们的组合物以及通过应用这些组合物来控制杂草的方法。这些杀草化合物是公式的2-[(4-杂环(苯氧甲基)苯氧基]脂肪酸酯：##STR1## 其中，A是与苯氧基氧原子在α碳上结合的脂肪酸酯衍生物，Q是4-二氟甲基-4,5-二氢-3-甲基-1,2,4-三唑-5(1H)-酮-1-基、3,4,5,6-四氢邻酰胺-1-基、1-(1-甲基乙基)咪唑烷-2,4-二酮-3-基、1,4-二氢-4-(3-氟丙基)-5H-四唑-5-酮-1-基、3-氯-4,5,6,7-四氢吲哚-2-基、4-甲基-1,2,4-三嗪-3,5-二酮-2-基、8-硫代-1,6-二氮杂双环[4.3.0]壬烷-7-酮-9-亚胺基或1-甲基-6-三氟甲基-2,4-嘧啶二酮-3-基；X是氢、氟或氯；Y是氢；W是氧或硫；Z是氢、氟、氯、溴、低碳基或甲氧基；Z'是氢、氟或氯；AO-基团可以在苯环上的2、3或4位置。

  公开号：

  US05262390A1

文献信息

• Herbicidal combinations containing
  申请人：——

  公开号：US05798316A1

  公开（公告）日：1998-08-25

  Herbicidal compositions containing herbicidal 2-\x9b(4-heterocyclic-phenoxymethyl)phenoxy!alkanoates in combination with other herbicides are disclosed. The herbicidal 2-\x9b(4-heterocyclic-phenoxymethyl)phenoxy!-alkanoates are of the formula ##STR1## in which R' is methyl, W is oxygen, Q is ##STR2## R is hydrogen, M, lower alkyl; cycloalkyl comprising from 3 to 6 carbon atoms; lower alkenyl; or lower alkynyleach optionally substituted with one or more chlorine or fluorine, or --\x9bCHR.sup.7 --(CH.sub.2).sub.m O!.sub.n R.sup.8 ; each of R.sup.1 through R.sup.5 is lower alkyl or lower haloalkyl; R.sup.6 is lower alkyl, lower haloalkyl, lower cyano-alkyl, lower alkoxyalkyl, lower alkoxycarbonylalkyl, lower arylalkyl, or amino; R.sup.7 is hydrogen or methyl; R.sup.8 is lower alkyl; X is hydrogen, methyl, fluorine, or chlorine; Y is hydrogen; Z is hydrogen, fluorine, chlorine, bromine, lower alkyl, or methoxy; Z' is hydrogen, fluorine, or chlorine; Z and Z' taken together may be --(CH.sub.2).sub.4 -- to form a tetrahydronaphthyl moiety; m is 0 to 2, and n is 1 to 6; and M is sodium, potassium or ammonium. These herbicidal alkanoates are used with either grass-controlling or broadleaf herbicides.

  含有杀草剂2-(4-杂环苯氧甲基)苯氧基!-癸酸酯的除草剂组合物与其他除草剂的组合物被揭示。这些杀草剂2-(4-杂环苯氧甲基)苯氧基!-癸酸酯的化学式为##STR1##其中R'为甲基，W为氧，Q为##STR2##R为氢，M，较低的烷基；由3到6个碳原子组成的环烷基；较低的烯基；或较低的炔基，每个选项都可以用一个或多个氯或氟取代，或--CHR.sup.7 --(CH.sub.2).sub.m O!.sub.n R.sup.8；R.sup.1到R.sup.5中的每一个都是较低的烷基或较低的卤代烷基；R.sup.6是较低的烷基，较低的卤代烷基，较低的氰基烷基，较低的烷氧基烷基，较低的烷氧羰基烷基，较低的芳基烷基，或氨基；R.sup.7是氢或甲基；R.sup.8是较低的烷基；X是氢，甲基，氟或氯；Y是氢；Z是氢，氟，氯，溴，较低的烷基或甲氧基；Z'是氢，氟或氯；Z和Z'一起可以是--(CH.sub.2).sub.4 --形成四氢萘基；m为0到2，n为1到6；M为钠，钾或铵。这些杀草剂癸酸酯与控制草类或阔叶杂草的除草剂一起使用。
• Herbicidal 2-[(4-heterocyclic-phenoxymethyl)phenoxy]-alkanoates
  申请人：FMC Corporation

  公开号：US05344812A1

  公开（公告）日：1994-09-06

  Herbicidal compounds, compositions containing them, and a method for controlling weeds by application of the compositions are disclosed. The herbicidal compounds are 2-[(4-heterocyclic-phenoxymethyl)phenoxy]alkanoates of the formula ##STR1## in which A is a derivative of an alkanoate bonded to the phenoxy oxygen at the alpha carbon, and Q is 4-difluoromethyl-4,5-dihydro-3-methyl-l,2,4-triazol-5(1H)-on-1-yl, 3,4,5,6-tetrahydrophthalimid-1-yl, 1-(1-methylethyl)imidazolidin-2,4-dion-3-yl, 1,4-dihydro-4-(3-fluoropropyl)-5H-tetrazol-5-on-1-yl, 3-chloro-4,5,6,7-tetrahydroindazol-2-yl, 4-methyl-l,2,4-triazine-3,5-dion-2-yl, 8-thia-1,6-diazabicyclo[4.3.0]-nonane-7-on-9-ylimino, or 1-methyl-6-trifluoromethyl-2,4-pyrimidinedione-3-yl; X is hydrogen, methyl, fluorine, or chlorine; Y is hydrogen; W is oxygen or sulfur; Z is hydrogen, fluorine, chlorine, bromine, lower alkyl, or methoxy; Z' is hydrogen, fluorine, or chlorine; and the group AO-- may be in the 2, 3, or 4-position of the phenyl ring.

  除草化合物、含有这些化合物的组合物以及通过应用这些组合物来控制杂草的方法被披露。这些除草化合物是具有以下式子的2-[(4-杂环-苯氧甲基)苯氧基]烷酸酯：##STR1## 其中A是与苯氧氧原子在α碳上结合的烷酸酯的衍生物，Q是4-二氟甲基-4,5-二氢-3-甲基-1,2,4-三唑-5(1H)-酮-1-基，3,4,5,6-四氢邻苯二甲酰亚胺-1-基，1-(1-甲基乙基)咪唑啉-2,4-二酮-3-基，1,4-二氢-4-(3-氟丙基)-5H-四唑-5-酮-1-基，3-氯-4,5,6,7-四氢吲哚-2-基，4-甲基-1,2,4-三嗪-3,5-二酮-2-基，8-硫代-1,6-二氮杂双环[4.3.0]-壬烷-7-酮-9-亚基，或1-甲基-6-三氟甲基-2,4-嘧啶二酮-3-基；X是氢、甲基、氟或氯；Y是氢；W是氧或硫；Z是氢、氟、氯、溴、低碳基或甲氧基；Z'是氢、氟或氯；以及AO--基团可能位于苯环的2、3或4位。
• [EN] N-ACYLAMINOBENZENE DERVATIVES AS SELECTIVE MONOAMINE OXIDASE B INHIBITORS<br/>[FR] DERIVES DE N-ACYLAMINOBENZENE COMME INHIBITEURS DE LA MONOAMINE OXYDASE B SELECTIFS
  申请人：HOFFMANN LA ROCHE

  公开号：WO2003099763A1

  公开（公告）日：2003-12-04

  This invention relates to N-acylamino aryl derivatives of the general formula (I), wherein R1 is halogen, halogen-(C1-C6)-alkyl, cyano, C1-C6-alkoxy or halogen-(C1-C6)-alkoxy; R21, R22, R23 and R24 independently from each other are selected from the group consisting of hydrogen, (C1-C6)-alkyl, halogen, halogen-(C1-C6)-alkyl, hydroxy, C1-C6-alkoxy or -CHO; R3 is hydrogen or C1-C3-alkyl; R4, R5 independently from each other are selected from the group consisting of hydrogen, C1-C6-alkyl, C1-C6-alkoxy or -COO(C1-C6)alkyl; or R4 and R5 form together with the C-atom to which they are attach a C3-C7-cycloalkyl ring; R6 is -CO-NR7R8; -COO(C1-C6)-alkyl, -CN, -NR2 or -NHC(O)R; R7 and R8 independently from each other are selected from the group consisting of hydrogen, C1-C6-alkyl, NH2 or hydroxy; R is hydrogen or C1-C6-alkyl; n is 0, 1, 2 or 3. X is -CHRO, -OCHR, -CH2S-, -SCH2-, -CH2CH2-, -CH=CH- or -C≡C-; and to pharmaceutically active acid addition salts thereof. It has been found that the compounds of general formula (I) are selective monoamine oxidase B inhibitors and they are therefore useful in the treatment of diseases mediated by monoamine oxidase B inhibitors, for example for the treatment of Alzheimer’s disease or senile dementia.

  这项发明涉及一般式(I)的N-酰氨基芳基衍生物，其中R1是卤素，卤代-(C1-C6)-烷基，氰基，C1-C6-烷氧基或卤代-(C1-C6)-烷氧基；R21、R22、R23和R24彼此独立地选自氢，(C1-C6)-烷基，卤素，卤代-(C1-C6)-烷基，羟基，C1-C6-烷氧基或-CHO的群；R3是氢或C1-C3-烷基；R4、R5彼此独立地选自氢，C1-C6-烷基，C1-C6-烷氧基或-COO(C1-C6)烷基的群；或R4和R5与它们连接的C原子一起形成一个C3-C7-环烷基环；R6是-CO-NR7R8；-COO(C1-C6)-烷基，-CN，-NR2或-NHC(O)R；R7和R8彼此独立地选自氢，C1-C6-烷基，NH2或羟基；R是氢或C1-C6-烷基；n为0、1、2或3。X是-CHRO，-OCHR，-CH2S-，-SCH2-，-CH2CH2-，-CH=CH-或-C≡C-；以及其药用活性酸盐。已发现一般式(I)的化合物是选择性单胺氧化酶B抑制剂，因此它们在治疗由单胺氧化酶B抑制剂介导的疾病中很有用，例如用于治疗阿尔茨海默病或老年性痴呆症。
• BENZYLOXY ANILIDE DERIVATIVES USEFUL AS POTASSIUM CHANNEL MODULATORS
  申请人：Wu Jim Zhen

  公开号：US20090326059A1

  公开（公告）日：2009-12-31

  The present invention relates to benzyloxyanilide derivatives having the following structural formula: The compounds of the present invention are useful for the treatment and prevention of diseases and disorders which are affected by activation or modulation of potassium ion channels. One such condition is seizure disorders.

  本发明涉及具有以下结构式的苯甲氧基苯胺衍生物：本发明的化合物可用于治疗和预防受钾离子通道激活或调节影响的疾病和疾病。其中一种病症是癫痫症。
• Herbicidal compositions comprising
  申请人：FMC Corporation

  公开号：US05674810A1

  公开（公告）日：1997-10-07

  Herbicidal compounds, compositions containing them, and a method for controlling weeds by application of the compositions are disclosed. The herbicidal compounds are 2-\x9b(4-heterocyclic-phenoxymethyl)phenoxy!alkanoates of the formula ##STR1## in which A is a derivative of an alkanoate bonded to the phenoxy oxygen at the alpha carbon; X is hydrogen, methyl, fluorine, or chlorine; Y is hydrogen; W is oxygen or sulfur; Z is hydrogen, fluorine, chlorine, bromine, lower alkyl, or methoxy; Z' is hydrogen, fluorine, or chlorine; and the group AO-- may be in the 2, 3, or 4-position of the phenyl ring.

  本发明揭示了除草化合物、含有它们的组合物以及通过应用这些组合物控制杂草的方法。除草化合物是公式2- \ x9b（4-杂环-苯氧甲基）苯氧基！脂肪酸盐，其中A是与苯氧氧原子在α碳上结合的脂肪酸盐的衍生物；X是氢、甲基、氟或氯；Y是氢；W是氧或硫；Z是氢、氟、氯、溴、低碳基或甲氧基；Z'是氢、氟或氯；并且AO-基团可以位于苯环的2、3或4位置。