tert-butyl 3-[(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)oxy]pyrrolidine-1-carboxylate | 186202-34-6

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 异吲哚及其衍生物
• 英文名称: tert-butyl 3-[(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)oxy]pyrrolidine-1-carboxylate
• 英文别名: (RS) 1-tert-butoxycarbonyl-3-phthalimidoxypyrrolidine；tert-butyl 3-(1,3-dioxoisoindol-2-yl)oxypyrrolidine-1-carboxylate
• CAS: 186202-34-6
• 化学式: C₁₇H₂₀N₂O₅
• 分子量: 332.356
• InChiKey: XJMZVQVTRJUZNV-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2
• 重原子数：
  24
• 可旋转键数：
  4
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.47
• 拓扑面积：
  76.2
• 氢给体数：
  0
• 氢受体数：
  5

反应信息

• 作为反应物：
  描述：

  tert-butyl 3-[(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)oxy]pyrrolidine-1-carboxylate 在 甲基肼 作用下， 以 甲醇 、 二氯甲烷 为溶剂， 反应 2.0h， 以76%的产率得到tert-butyl 3-(aminooxy)-1-pyrrolidinecarboxylate
  参考文献：
  名称：

  [EN] 6-AZAINDOLE COMPOUND
  [FR] COMPOSE DE 6-AZAINDOLE

  摘要：

  公开号：

  WO2005097129A3
• 作为产物：
  描述：

  二碳酸二叔丁酯 在 4-二甲氨基吡啶 、 三乙胺 、 三苯基膦 、 偶氮二甲酸二乙酯 作用下， 以 四氢呋喃 、 二氯甲烷 为溶剂， 反应 77.0h， 生成 tert-butyl 3-[(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)oxy]pyrrolidine-1-carboxylate
  参考文献：
  名称：

  [EN] 6-AZAINDOLE COMPOUND
  [FR] COMPOSE DE 6-AZAINDOLE

  摘要：

  公开号：

  WO2005097129A3

文献信息

• 6-Azaindole Compound
  申请人：Horiguchi Yoshiaki

  公开号：US20080064715A1

  公开（公告）日：2008-03-13

  A compound represented by the formula wherein R 1 , R 2 , R 3 and R 6 are the same or different and each is a hydrogen atom or a substituent; one of R 4 and R 5 is a hydrogen atom and the other is a group represented by the formula: —C(═X)—R 7 wherein X is N—O—R 8 or N—NH—R 9 wherein R 8 and R 9 are the same or different and each is a hydrogen atom or a group bonded via a carbon atom; and R 7 is a hydrogen atom or a substituent, and the like and a salt thereof have a superior IκB kinase inhibitory activity, and useful as pharmaceutical agents such as agents for preventing or treating diabetes and the like.

  一种化合物的化学式为其中R1、R2、R3和R6相同或不同，每个都是氢原子或取代基；R4和R5中的一个是氢原子，另一个是代表公式的基团：—C(═X)—R7，其中X为N—O—R8或N—NH—R9，R8和R9相同或不同，每个都是氢原子或通过碳原子键合的基团；而R7是氢原子或取代基等。该化合物及其盐具有优异的IκB激酶抑制活性，并可用作预防或治疗糖尿病等药物。
• Aza-benzofuranyl compounds and methods of use
  申请人：Savy Pierre Pascal

  公开号：US20080085886A1

  公开（公告）日：2008-04-10

  The invention relates to azabenzofuranyl compounds of Formula I with anti-cancer and/or anti-inflammatory activity and more specifically to azabenzofuranyl compounds which inhibit MEK kinase activity. The invention provides compositions and methods useful for inhibiting abnormal cell growth or treating a hyperproliferative disorder, or treating an inflammatory disease in a mammal. The invention also relates to methods of using the compounds for in vitro, in situ, and in vivo diagnosis or treatment of mammalian cells, or associated pathological conditions.

  本发明涉及具有抗癌和/或抗炎活性的Formula I的氮杂苯并呋喃化合物，更具体地涉及抑制MEK激酶活性的氮杂苯并呋喃化合物。本发明提供了用于抑制异常细胞生长或治疗哺乳动物的增生性疾病或治疗炎症性疾病的组合物和方法。本发明还涉及使用该化合物进行哺乳动物细胞的体外、原位和体内诊断或治疗，或相关病理条件的方法。
• AZA-INDOLYL COMPOUNDS AND METHODS OF USE
  申请人：Goodacre Simon Charles

  公开号：US20080242655A1

  公开（公告）日：2008-10-02

  The invention relates to azaindolyl compounds of Formula I with anti-cancer and/or anti-inflammatory activity and more specifically to azaindolyl compounds which inhibit MEK kinase activity. The invention provides compositions and methods useful for inhibiting abnormal cell growth or treating a hyperproliferative disorder, or treating an inflammatory disease in a mammal. The invention also relates to methods of using the compounds for in vitro, in situ, and in vivo diagnosis or treatment of mammalian cells, or associated pathological conditions.

  本发明涉及具有抗癌和/或抗炎活性的Formula I的吡唑吲哚类化合物，更具体地涉及抑制MEK激酶活性的吡唑吲哚类化合物。本发明提供了用于抑制异常细胞生长或治疗哺乳动物的增生性疾病或治疗炎症性疾病的组合物和方法。本发明还涉及使用该化合物进行哺乳动物细胞的体外、原位和体内诊断或治疗，或相关病理条件的方法。
• OXYCARBAMOYL COMPOUNDS AND THE USE THEREOF
  申请人：Mikamiyama Hidenori

  公开号：US20110098276A1

  公开（公告）日：2011-04-28

  The invention relates to oxycarbamoyl compounds of Formula I: The invention is also directed to the use compounds of Formula I to treat, prevent or ameliorate a disorder responsive to the blockade of calcium channels, and particularly N-type calcium channels. Compounds of the present invention are especially useful for treating pain.

  本发明涉及式I的氧化氨基甲酰化合物：本发明还涉及使用式I的化合物来治疗、预防或改善对钙通道阻滞有反应的疾病，尤其是N型钙通道。本发明的化合物特别适用于治疗疼痛。
• 6-azaindole compound
  申请人：Takeda Pharmaceutical Company Limited

  公开号：US07608627B2

  公开（公告）日：2009-10-27

  A compound represented by the formula wherein R1, R2, R3 and R6 are the same or different and each is a hydrogen atom or a substituent; one of R4 and R5 is a hydrogen atom and the other is a group represented by the formula: —C(═X)—R7 wherein X is N—O—R8 or N—NH—R9 wherein R8 and R9 are the same or different and each is a hydrogen atom or a group bonded via a carbon atom; and R7 is a hydrogen atom or a substituent, and the like and a salt thereof have a superior IκB kinase inhibitory activity, and useful as pharmaceutical agents such as agents for preventing or treating diabetes and the like.

  该化合物的化学式表示为其中R1，R2，R3和R6相同或不同，每个都是氢原子或取代基; R4和R5中的一个是氢原子，另一个是表示为公式的基团：—C（═X）—R7，其中X为N—O—R8或N—NH—R9，其中R8和R9相同或不同，每个都是氢原子或通过碳原子连接的基团; R7是氢原子或取代基，类似物及其盐具有优良的IκB激酶抑制活性，并可用作预防或治疗糖尿病等药物。