4-(5-methylpyridin-2-yloxy)-N-Boc-piperidine | 939986-12-6

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 哌啶类
• 英文名称: 4-(5-methylpyridin-2-yloxy)-N-Boc-piperidine
• 英文别名: tert-Butyl 4-((5-methylpyridin-2-yl)oxy)piperidine-1-carboxylate；tert-butyl 4-(5-methylpyridin-2-yl)oxypiperidine-1-carboxylate
• CAS: 939986-12-6
• 化学式: C₁₆H₂₄N₂O₃
• 分子量: 292.378
• InChiKey: PCXPQDLRPKMOAD-UHFFFAOYSA-N

物化性质

• 沸点：
  395.6±42.0 °C(Predicted)
• 密度：
  1.108

计算性质

• 辛醇/水分配系数(LogP)：
  3
• 重原子数：
  21
• 可旋转键数：
  4
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.62
• 拓扑面积：
  51.7
• 氢给体数：
  0
• 氢受体数：
  4

文献信息

• Pyrazole Derivatives for the Inhibition of CDK'S and GSK'S
  申请人：Wyatt Paul Graham

  公开号：US20080306069A1

  公开（公告）日：2008-12-11

  The invention provides compounds of the formula (I), or salts, tautomers, N-oxides or solvates thereof wherein: R1 is selected from: (a) 2,6-dichlorophenyl; (b) 2,6-difluorophenyl; (c) a 2,3,6-trisubstituted phenyl group wherein the substituents for the phenyl group are selected from fluorine, chlorine, methyl and methoxy; (d) a group RO; (e) a group R a; (f) a group RIb; (g) a group RIc; (h) a group RId; and 0) 2,6-difluorophenylamino; wherein R) 0υ, r R>llaa, T Rj HbD, T R) HcC, r R>Iidα, r R>>2zaa, r R>22bD and RJ are as defined in the claims. The compounds have activity as inhibitors of cdk kinase (such as cdk1 or cdk2) and glycogen synthase kinase-3 activity.

  该发明提供了式(I)的化合物，或其盐、互变异构体、N-氧化物或溶剂化物，其中：R1选择自：(a)2,6-二氯苯基；(b)2,6-二氟苯基；(c)2,3,6-三取代苯基，其中苯基的取代基选择自氟、氯、甲基和甲氧基；(d)羟基取代基；(e)R a基；(f)RIb基；(g)RIc基；(h)RId基；和(i)2,6-二氟苯基氨基基；其中R) 0υ，r R>llaa，T Rj HbD，T R) HcC，r R>Iidα，r R>>2zaa，r R>22bD和RJ如权利要求所定义。该化合物具有作为cdk激酶（如cdk1或cdk2）和糖原合成酶激酶-3活性抑制剂的活性。
• Novel heterocyclic compound
  申请人：Kodo Toru

  公开号：US20070191447A1

  公开（公告）日：2007-08-16

  A drug having a high affinity for benzodiazepine ω 3 receptors and showing curative and preventive effects for anxiety and depression, which comprises as the active ingredient, for example, a compound of the formula (1): wherein R 1 and R 2 are independently a hydrogen atom, an optionally substituted alkyl group, an optionally substituted aryl group, etc., R 3 and R 4 are independently a hydrogen atom, an optionally substituted alkyl group, etc., R 5 , R 6 , R 7 and R 8 are independently a hydrogen atom, an optionally substituted alkyl group, an optionally substituted aryl group, etc., X is an oxygen atom, a sulfur atom, NR 10 , etc. (in which R 10 is a hydrogen atom, an optionally substituted alkyl group, etc.)

  一种对苯二氮平ω3受体具有高亲和力，对焦虑和抑郁具有治疗和预防效果的药物，其包括作为活性成分的化合物，例如式（1）的化合物： 其中R1和R2分别为氢原子，可选取代烷基，可选取代芳基等； R3和R4分别为氢原子，可选取代烷基等； R5、R6、R7和R8分别为氢原子，可选取代烷基，可选取代芳基等； X为氧原子、硫原子、NR10等（其中R10为氢原子、可选取代烷基等）。