diethyl 2-[4-nitro-3-(trifluoromethyl)phenyl]propanedioate | 885498-68-0

• 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: diethyl 2-[4-nitro-3-(trifluoromethyl)phenyl]propanedioate
• 英文别名: diethyl 2-(4-nitro-3-trifluoromethyl-phenyl)-malonate
• CAS: 885498-68-0
• 化学式: C₁₄H₁₄F₃NO₆
• 分子量: 349.263
• InChiKey: NXNWPRIPAMNYMQ-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.3
• 重原子数：
  24
• 可旋转键数：
  7
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.43
• 拓扑面积：
  98.4
• 氢给体数：
  0
• 氢受体数：
  9

反应信息

• 作为反应物：
  描述：

  diethyl 2-[4-nitro-3-(trifluoromethyl)phenyl]propanedioate 在 palladium-carbon diethyl 2-[4-amino-3-(trifluoromethyl)phenyl]propanedioate 作用下， 以 乙酸乙酯 为溶剂， 以had been obtained in 1), and the solution的产率得到diethyl 2-[4-amino-3-(trifluoromethyl)phenyl]propanedioate
  参考文献：
  名称：

  3-carbamoyl-2-pyridone derivatives

  摘要：

  本发明提供了具有作用于大麻素受体的激动活性的化合物，其由式（I）所表示，其中R1、R2、R3、R4和G如本文所定义，其为药学上可接受的盐或其溶剂，以及含有该化合物作为活性成分的药物组合物、用于治疗特应性皮炎的药物、抗瘙痒药物，特别是用于口服和外用的抗瘙痒药物。

  公开号：

  US08367666B2
• 作为产物：
  描述：

  5-氟-2-硝基三氟甲苯 、 丙二酸二乙酯 在 sodium hydride 作用下， 以 N,N-二甲基甲酰胺 为溶剂， 生成 diethyl 2-[4-nitro-3-(trifluoromethyl)phenyl]propanedioate
  参考文献：
  名称：

  [EN] NITROGEN-CONTAINING HETEROCYCLIC DERIVATIVE, AND COMPOSITION AND PHARMACEUTICAL APPLICATION THEREOF
  [FR] DÉRIVÉ HÉTÉROCYCLIQUE AZOTÉ ET COMPOSITION ET APPLICATION PHARMACEUTIQUE ASSOCIÉES
  [ZH] 一种含氮杂环衍生物及其组合物和药学上的应用

  摘要：

  本发明涉及一种通式(I)所述的化合物或者其立体异构体、氘代物、溶剂化物、前药、代谢产物、药学上可接受的盐或共晶，及其中间体，以及在AR相关疾病如癌症中的用途。 B-L-K (I)

  公开号：

  WO2023208165A1

文献信息

• 3-Carbamoyl-2-Pyridone Derivative
  申请人：Ishizuka Natsuki

  公开号：US20080103139A1

  公开（公告）日：2008-05-01

  The present invention provides compounds having an agonistic activity to the cannabinoid receptor, which is represented by the formula (I): wherein R 1 is optionally substituted C1-C8 alkyl and the like; R 2 is C1-C6 alkyl; R 3 is C1-C6 alkyl and the like; or R 2 and R 3 taken together with may form an optionally substituted 5 to 10 membered non-aromatic carbon ring; R 4 is hydrogen and the like; G is a group selected from the groups shown by the formula an the like: wherein R 5 is hydrogen and the like; X 1 is a single bond and the like; X 2 is optionally substituted C1-C8 alkylene that may be replaced by one or two groups of —O—, or —N(R 6 )—, wherein R 6 is hydrogen and the like, and the like; X 3 is a single bond and the like; a pharmaceutically acceptable salt or a solvate thereof, and pharmaceutical compositions, atopic dermatitis treating agents, and anti-pruritus agents, especially anti-pruritus agents for oral used and for external application, which each contains the said compound as an active ingredient.

  本发明提供了具有激动大麻素受体的作用的化合物，其由式（I）表示：其中，R1是可选取的取代的C1-C8烷基等；R2是C1-C6烷基；R3是C1-C6烷基等；或R2和R3共同形成可选取代的5至10个成员的非芳香碳环；R4是氢等；G是由式等所示的基团中选取的基团：其中，R5是氢等；X1是单键等；X2是可选取代的C1-C8烷基，可以被一或两个-O-或-N（R6）-的基团替代，其中R6是氢等；X3是单键等；其药学上可接受的盐或其溶剂，以及制药组合物、治疗特应性皮炎的制剂和抗瘙痒剂，特别是口服和外用的抗瘙痒剂，每种制剂均以所述化合物为活性成分。
• 3-carbamoyl-2-pyridone derivatives
  申请人：Shionogi & Co., Ltd.

  公开号：US08178681B2

  公开（公告）日：2012-05-15

  The present invention provides compounds having an agonistic activity to the cannabinoid receptor, which is represented by the formula (I): wherein R1 is optionally substituted C1-C8 alkyl and the like; R2 is C1-C6 alkyl; R3 is C1-C6 alkyl and the like; or R2 and R3 taken together with may form an optionally substituted 5 to 10 membered non-aromatic carbon ring; R4 is hydrogen and the like; G is a group selected from the groups shown by the formula an the like: wherein R5 is hydrogen and the like; X1 is a single bond and the like; X2 is optionally substituted C1-C8 alkylene that may be replaced by one or two groups of —O—, or —N(R6)—, wherein R6 is hydrogen and the like, and the like; X3 is a single bond and the like; a pharmaceutically acceptable salt or a solvate thereof, and pharmaceutical compositions, atopic dermatitis treating agents, and anti-pruritus agents, especially anti-pruritus agents for oral used and for external application, which each contains the said compound as an active ingredient.

  本发明提供了具有类脑受体激动活性的化合物，其由式（I）所表示：其中R1是可选取代的C1-C8烷基等；R2是C1-C6烷基；R3是C1-C6烷基等；或R2和R3结合在一起可以形成一个可选取代的5到10个成员的非芳香碳环；R4是氢等；G是通过式等所示的基团中选择的基团：其中R5是氢等；X1是单键等；X2是可选取代的C1-C8烷基，可以被一个或两个-O-或-N（R6）-等基团所代替，其中R6是氢等等；X3是单键等；以及含有所述化合物作为活性成分的药物学上可接受的盐或溶剂和制药组合物，特别是用于口服和外用的抗瘙痒剂和特应性皮炎治疗剂。
• 3-CARBAMOYL-2-PYRIDONE DERIVATIVES
  申请人：ISHIZUKA Natsuki

  公开号：US20120208813A1

  公开（公告）日：2012-08-16

  The present invention provides compounds having an agonistic activity to the cannabinoid receptor, which is represented by the formula (I): wherein R 1 , R 2 , R 3 , R 4 , and G are defined as herein, a pharmaceutically acceptable salt or a solvate thereof, and pharmaceutical compositions, atopic dermatitis treating agents, and anti-pruritus agents, especially anti-pruritus agents for oral used and for external application, which each contains the said compound as an active ingredient.

  本发明提供了具有激动大麻素受体的活性的化合物，该受体由公式（I）表示：其中R1、R2、R3、R4和G如本文所定义，其药学上可接受的盐或溶剂，以及制备该化合物为活性成分的药物组合物、治疗特应性皮炎的药剂和抗瘙痒剂，尤其是用于口服和外用的抗瘙痒剂。
• 3-CARBAMOYL-2-PYRIDONE DERIVATIVE
  申请人：SHIONOGI & CO., LTD.

  公开号：EP1806342B1

  公开（公告）日：2013-04-17
• US8178681B2
  申请人：——

  公开号：US8178681B2

  公开（公告）日：2012-05-15