4-methoxy-2-(2-methoxy-ethyl)-N-(tetrahydro-pyran-2-yloxy)-2-[4-(4-trifluoromethylsulfanyl-phenoxy)-piperidine-1-sulfonyl]-butyramide | 851771-31-8

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯酚醚
• 英文名称: 4-methoxy-2-(2-methoxy-ethyl)-N-(tetrahydro-pyran-2-yloxy)-2-[4-(4-trifluoromethylsulfanyl-phenoxy)-piperidine-1-sulfonyl]-butyramide
• 英文别名: 4-methoxy-2-(2-methoxyethyl)-N-(oxan-2-yloxy)-2-[4-[4-(trifluoromethylsulfanyl)phenoxy]piperidin-1-yl]sulfonylbutanamide
• CAS: 851771-31-8
• 化学式: C₂₅H₃₇F₃N₂O₈S₂
• 分子量: 614.705
• InChiKey: YIMMTTNAFGSOLV-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4
• 重原子数：
  40
• 可旋转键数：
  14
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.72
• 拓扑面积：
  146
• 氢给体数：
  1
• 氢受体数：
  13

反应信息

• 作为反应物：
  描述：

  4-methoxy-2-(2-methoxy-ethyl)-N-(tetrahydro-pyran-2-yloxy)-2-[4-(4-trifluoromethylsulfanyl-phenoxy)-piperidine-1-sulfonyl]-butyramide 以 盐酸 、 甲醇 、 水 、 乙酸乙酯 、 乙腈 为溶剂， 以100%的产率得到N-hydroxy-4-methoxy-2-(2-methoxyethyl)-2-[(4-{4-[(trifluoromethyl)thio]phenoxy}piperidin-1-yl)sulfonyl]butanamide
  参考文献：
  名称：

  Piperidinyl- and piperazinyl-sulfonylmethyl hydroxamic acids and their use as protease inhibitors

  摘要：

  这项发明通常涉及蛋白酶抑制剂（也称为“蛋白酶”），更具体地涉及哌啶基和哌嗪基磺酰甲基羟肟酸，该类化合物在结构上抑制基质金属蛋白酶（也称为“基质金属蛋白酶”或“MMP”）活性和/或聚集素酶活性。这类羟肟酸通常对应以下结构式： （其中A1、A2、Y、E1、E2、E3和Rx如本说明书中所定义），还包括这类化合物的盐。这项发明还涉及这类羟肟酸的组合物、合成这类羟肟酸的中间体、制备这类羟肟酸的方法，以及治疗与MMP活性和/或聚集素酶活性相关的疾病（特别是病理性疾病）的方法。

  公开号：

  US20050209278A1

文献信息

• 2-Phenyl-2h-pyridazine-3-ones
  申请人：——

  公开号：US20030162662A1

  公开（公告）日：2003-08-28

  The invention relates to 2-phenyl-2H-pyridazin-3-ones of the general formula I 1 in which the variables R 1 , R 2 , X, Y and Z have the following meanings: X is halogen; Y is fluorine or chlorine; Z is oxygen; R 1 is hydrogen or C 1 -C 4 -alkyl; R 2 is chlorine, OR 3 or NR 4 R 5 , in which R 3 , R 4 and R 5 have the meanings indicated in claim 1, Z can also be a group NR 6 if R 2 is a group OR 7 , in which R 6 and R 7 have the meanings indicated in claim 1, and to the agriculturally utilizable salts of compounds of the formula I. The invention furthermore relates to the use of compounds I and their salts as herbicides and/or for the desiccation and/or defoliation of plants, herbicidal compositions and compositions for the desiccation and/or defoliation of plants, which contain the compounds I and/or their salts as active substances, and processes for controlling undesired vegetation (weeds) and for the desiccation and/or defoliation of plants using the compounds I and/or their salts.

  该发明涉及一般式I中的2-苯基-2H-吡啶并三酮，其中变量R1、R2、X、Y和Z具有以下含义：X为卤素；Y为氟或氯；Z为氧；R1为氢或C1-C4-烷基；R2为氯、OR3或NR4R5，其中R3、R4和R5具有权利要求1中所指的含义，如果R2为OR7，则Z也可以是NR6基团，其中R6和R7具有权利要求1中所指的含义，并且该发明还涉及一般式I化合物的农业可利用盐。此外，该发明涉及将化合物I及其盐用作除草剂和/或用于植物脱水和/或落叶，含有化合物I和/或其盐作为活性物质的除草剂组合物和用于植物脱水和/或落叶的组合物，以及利用化合物I和/或其盐控制不受欢迎的植被（杂草）和对植物进行脱水和/或落叶的过程。
• Indole derivatives
  申请人：Yamasaki Noritsugu

  公开号：US20050171185A1

  公开（公告）日：2005-08-04

  A novel indole derivative or a salt thereof is provided, which is represented by the formula: wherein R 1 represents an aryl lower alkyl group, said aryl group may be substituted with one or more groups selected from the group consisting of a halogen atom, an aryl group, a heterocyclic group, an aryl lower alkyl group, an aryl lower alkenyl group, a halo-lower alkyl group, a lower cycloalkyl-lower alkoxy group, a lower cycloalkoxy-lower alkyl group, an aryl lower alkynyl group, an aryloxy lower alkyl group, an aryl lower alkoxy group, a lower alkylthio group, a lower alkoxy group, and an alkenyl group; and R 2 represents a lower alkyl group, a lower alkenyl group, an aryl group, or a heterocyclic group, each of which may be substituted with a hydrogen atom, a lower alkyl group, a lower alkenyl group, or an aryl group. The compound of the present invention has blood sugar level-depressing activity and PDE5-inhibiting activity, and is useful as medicine.

  本发明提供了一种新的吲哚衍生物或其盐，其表示为以下公式：其中，R1表示芳基低烷基基团，所述芳基基团可以用以下一种或多种基团替代：卤原子、芳基基团、杂环基团、芳基低烷基基团、芳基低烯基基团、卤代低烷基基团、低环烷基低烷氧基团、低环烷氧基低烷基基团、芳基低炔基基团、芳氧基低烷基基团、芳基低烷氧基团、低烷基硫基团、低烷氧基团和烯基基团；R2表示低烷基基团、低烯基基团、芳基基团或杂环基团，每个基团可以用氢原子、低烷基基团、低烯基基团或芳基基团替代。本发明化合物具有降低血糖水平的活性和PDE5抑制活性，并可用作药物。
• BENZIMIDAZOLE DERIVATIVES
  申请人：FUJISAWA PHARMACEUTICAL CO., LTD.

  公开号：EP1020452A1

  公开（公告）日：2000-07-19

  A novel benzimidazole derivative or a salt thereof is provided, which is represented by the formula: wherein R1 represents an alkyl group, etc., R2 represents a substituted or unsubstituted aromatic lower alkyl group, R3 represents an alkyl group, etc., and -X- is represented by the following formula (V): etc. This derivative or a salt thereof is useful as medicine.

  本发明提供了一种新型苯并咪唑衍生物或其盐，由式表示： 其中 R1 代表烷基等，R2 代表取代或未取代的芳香族低级烷基，R3 代表烷基等，-X- 由下式（V）表示： 等。这种衍生物或其盐可用作药物。
• INDOLE DERIVATIVES
  申请人：FUJISAWA PHARMACEUTICAL CO., LTD.

  公开号：EP1070705A1

  公开（公告）日：2001-01-24

  Novel indole derivatives represented by formula (I) or salts thereof, wherein R1 is aryl-substituted lower alkyl in which the aryl may be substituted by at least one member selected among halogen atoms, aryls, heterocyclic groups, aryl-substituted lower alkyls, aryl-substituted lower alkenyls, lower haloalkyls, (lower cycloalkyl)-substituted lower alkyloxys, (lower cycloalkyloxy)-substituted lower alkyls, aryl-substituted lower alkynyls, aryloxy-substituted lower alkyls, aryl-substituted lower alkyloxys, lower alkylthios, lower alkyloxys, and alkenyls; and R2 is a lower alkyl, lower alkenyl, aryl, or heterocyclic group optionally substituted by halogeno, lower alkyl, lower alkenyl, or aryl. These compounds have a hypoglycemic activity and a PDE5 inhibitory activity and are useful as a drug.

  低级卤代烷基、（低级环烷基）取代的低级烷氧基、（低级环烷氧基）取代的低级烷基、芳基取代的低级炔基、芳氧基取代的低级烷基、芳基取代的低级烷氧基、低级烷硫基、低级烷氧基和烯基；R2 是可选被卤素、低级烷基、低级烯基或芳基取代的低级烷基、低级烯基、芳基或杂环基团。这些化合物具有降血糖活性和 PDE5 抑制活性，可用作药物。
• PIPERIDINYL-AND PIPERAZINYL-SULFONYLMETHYL HYDROXAMIC ACIDS AND THEIR USE AS PROTEASE INHIBITORS
  申请人：Pharmacia Corporation

  公开号：EP1689743A2

  公开（公告）日：2006-08-16