N-(4-fluorophenyl)-N'-(2-hydroxyethyl)thiourea | 344308-24-3

• 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: N-(4-fluorophenyl)-N'-(2-hydroxyethyl)thiourea
• 英文别名: 1-(4-Fluorophenyl)-3-(2-hydroxyethyl)thiourea
• CAS: 344308-24-3
• 化学式: C₉H₁₁FN₂OS
• mdl: MFCD01975349
• 分子量: 214.264
• InChiKey: FHOSFKLVCXFTBV-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  0.5
• 重原子数：
  14
• 可旋转键数：
  3
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.222
• 拓扑面积：
  76.4
• 氢给体数：
  3
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  N-(4-fluorophenyl)-N'-(2-hydroxyethyl)thiourea 在 盐酸 、 sodium hydride 作用下， 以 N,N-二甲基甲酰胺 、 乙腈 为溶剂， 反应 1.25h， 生成 N-(4-fluorophenyl)-3-[[6-[[2-(4-fluorophenyl)imino-1,3-thiazolidin-3-yl]methyl]pyridin-2-yl]methyl]-1,3-thiazolidin-2-imine
  参考文献：
  名称：

  Synthesis and Biological Activity of Novel Symmetrical Bis-2-phenyliminothiazolidine Derivatives

  摘要：

  A series of novel symmetrical bis-2-phenyliminothiazolidine derivatives were designed and synthesized. The structures of all the title compounds were characterized by H-1 NMR and, in some cases, by C-13 NMR, IR, and high-resolution mass spectra. Herbicidal activities were examined, and some of these compounds showed selectively herbicidal activity against Triticum aestivum. The type of linker between the two 2-phenyliminothiazolidines was crucial for the biological activities.

  DOI：

  10.1080/10426500600865103
• 作为产物：
  描述：

  4-氟苯胺 在 sodium hydroxide 作用下， 以 乙酸乙酯 为溶剂， 反应 24.67h， 生成 N-(4-fluorophenyl)-N'-(2-hydroxyethyl)thiourea
  参考文献：
  名称：

  Synthesis and fungicidal activity of fluorine-containing phenylimino-thiazolidines derivatives

  摘要：

  Nine new fluorine-containing phenylimino-thiazolidines derivatives were prepared. The structures of all compounds were confirmed by I H NMR, mass and high resolution mass spectroscopy. The antifungicidal activities of the title compounds on Phytophthoza capsici L., Pyriculazia ozyzae C., Fusazium spp. at 100 ppm were screened. (c) 2004 Elsevier B.V. All rights reserved.

  DOI：

  10.1016/j.jfluchem.2004.10.018

文献信息

• 2,3-Dihydro-imidazo[2,1-b]benzothiazole compositions to treat depressions
  申请人：Janssen Pharmaceutica, N.V.

  公开号：US04262004A1

  公开（公告）日：1981-04-14

  This invention relates to a novel series of 2,3-dihydro-imidazo[2,1-b]benzothiazoles which display monoamine oxidase inhibiting activities.

  这项发明涉及一种新颖的显示单胺氧化酶抑制活性的2,3-二氢咪唑并[2,1-b]苯并噻唑类化合物系列。
• 2,3-Dihydro-imidazo[2,1-b]benzothiazoles
  申请人：Janssen Pharmaceutica, N.V.

  公开号：US04340738A1

  公开（公告）日：1982-07-20

  This invention relates to a novel series of 2,3-dihydroimidazo[2,1-b]benzothiazoles which display monoamine oxidase inhibiting activities.

  本发明涉及一种新颖的2,3-二氢咪唑[2,1-b]苯并噻唑系列化合物，具有单胺氧化酶抑制活性。
• 2,3-Dihydro-imidazo (2,1-b)benzothiazoles compositions useful as
  申请人：Janssen Pharmaceutica N.V.

  公开号：US04364942A1

  公开（公告）日：1982-12-21

  This invention relates to a novel series of 2,3-dihydro-imidazo[2,1-b]benzothiazoles which display monoamine oxidase inhibiting activities.

  本发明涉及一种新颖的2,3-二氢咪唑[2,1-b]苯并噻唑系列化合物，其具有单胺氧化酶抑制活性。
• 2,3-Dihydro-imidazo (2,1-b) benzothiazole derivatives and pharmaceutical compositions containing them
  申请人：JANSSEN PHARMACEUTICA N.V.

  公开号：EP0021806A1

  公开（公告）日：1981-01-07

  Compounds of formula and the salts of formula wherein: R' and R3 are hydrogen and alkyl; R2 and R4 are hydrogen, alkyl, aryl, aralkyl, alkyloxyl alkyl or aryloxyl alkyl; R5, R6, R7 and R8 are hydrogen; halo; nitro; alkyl; cycloalkyl; hydroxy; alkyloxy; aryloxy; a-hydroxyaryl-methyl; amino; mono- and dialkyl-amino; mono-, di- and trihalo alkyl-amino; alkenylamino; alkynylamino; (aryl alkyl) amino; (alkyloxy alkyl)amino; (hydroxy alkyl)amino; (aryloxy alkyl)amino; (mono- and di(alkyl)amino-alkyl)amino; alkanoyl-amino; N-(alkyl)-alkanoylamino; aminocarbonylamino; (1-alkyl-4-piperidinyl)amino; cycloalkylamino wherein said cycloalkyl represents a mono-, bi-, tri- or tetracyclic hydrocarbon radical having from 3 to 10 carbon atoms; and a radical of the formula -N-CH=C(COO-alkyl)2 R10 wherein R'° is hydrogen, alkyl, alkenyl and alkynyl; or, when taken together R5and R6, R6and R8 or R7 and R8 may form a tri-or tetramethylene bridge or complete a fused benzene nucleus; R9 is alkyl, alkenyl, alkynyl and aryl alkyl; and X is a pharmaceutically acceptable anion and n represents the valency of the anion, display monoamine oxidase inhibiting properties.

  式化合物 和式盐 其中 R' 和 R3 是氢和烷基； R2 和 R4 是氢、烷基、芳基、芳烷基、烷氧基烷基或芳基烷基； R5、R6、R7 和 R8 是氢；卤素；硝基；烷基；环烷基；羟基；烷氧基；芳氧基；a-羟基芳基甲基；氨基；单和二烷基氨基；单、二和三卤代烷基氨基；烯基氨基；炔基氨基；（芳基烷基）氨基；（烷氧基烷基）氨基；（羟基烷基）氨基；（芳氧基烷基）氨基；(单-和二(烷基)氨基-烷基)氨基；烷酰氨基；N-(烷基)-烷酰氨基；氨基羰基氨基；(1-烷基-4-哌啶基)氨基；环烷基氨基，其中所述环烷基代表具有 3 至 10 个碳原子的单环、双环、三环或四环烃基；以及式 -N-CH=C(COO- 烷基)2R10的基团 其中 R'° 是氢、烷基、烯基和炔基；或者，当 R5 和 R6、R6 和 R8 或 R7 和 R8 结合在一起时，可形成三或四亚甲基桥或完整的融合苯核；R9 是烷基、烯基、炔基和芳基烷基；X 是药学上可接受的阴离子，n 代表阴离子的价数，具有单胺氧化酶抑制特性。
• Syntheses, structures and bioactivities of fluorine-containing phenylimino-thia(oxa)zolidine derivatives as agricultural bioregulators
  作者：Xuhong Qian、Xiaoyong Xu、Zhibin Li、Zhong Li、Gonghua Song

  DOI：10.1016/j.jfluchem.2004.09.002

  日期：2004.11

  From insight into the structure of trehazolin as trehalase inhibitor, six series of fluorine-containing phenylimino-thiazolidines (oxazolidines) derivatives were designed and prepared through a convenient synthesis of fluoroaryl isothiocyanate and a one-pot facile synthesis in high yield of fluorophenyl aminobenzoxazoles by cyclodesulfurization. The structures of the target compounds were confirmed with using IR, NMR, MS and elemental analysis. Their X-ray crystal analysis suggested that there were novel intermolecular (sp(2)CF(...)H(3)C-) and intramolecular (sp(2)CF(...)HN) hydrogen bonds between the fluorine atom on benzene ring and hydrogen atom of methyl group or amino group on five-membered heterocycle. Their fungicidal activities against Rhizoctonia solani and Pyricuraria oryzae at 100 ppm were determined. (C) 2004 Elsevier B.V. All rights reserved.