2-环己基氨基-4,6-二氯-1,3,5-三嗪 | 1036583-07-9

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 中文名称: 2-环己基氨基-4,6-二氯-1,3,5-三嗪
• 英文名称: 2-cyclohexylamino-4,6-dichloro-1,3,5-triazine
• 英文别名: 3,5-dichloro-N-cyclohexylaniline
• CAS: 1036583-07-9
• 化学式: C₁₂H₁₅Cl₂N
• 分子量: 244.164
• InChiKey: KSHJAKAQLNGALB-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  5
• 重原子数：
  15
• 可旋转键数：
  2
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.5
• 拓扑面积：
  12
• 氢给体数：
  1
• 氢受体数：
  1

反应信息

• 作为反应物：
  描述：

  2-环己基氨基-4,6-二氯-1,3,5-三嗪 、 1-Boc-3-甲基哌嗪 在 N,N-二异丙基乙胺 作用下， 以 二氯甲烷 为溶剂， 反应 1.0h， 生成 2-chloro-4-cyclohexylamino-6-(4-tert-butoxycarbonyl-2-methylpiperazin-1-yl)-1,3,5-triazine
  参考文献：
  名称：

  [EN] 2-CYANO-1,3,5-TRIAZINE-4,6-DIAMINE DERIVATIVES
  [FR] DERIVES 2-CYANO-1,3,5-TRIAZINE-4,6-DIAMINES

  摘要：

  该发明涉及使用具有通式（I）的2-氰基-1,3,5-三嗪-4,6-二胺衍生物，其中R1为（C1-6）烷基，（C3-8）环烷基，芳基，芳基（C1-4）烷基，芳氧基（C1-4）烷基，杂芳基或杂芳氧基（C1-4）烷基；R2为H或（C1-4）烷基；或R1和R2与它们结合的氮一起形成一个4-8元杂环，可进一步包括1个或多个来自O、S或NR5的杂原子，该环可能被（C1-4）烷基，（C3-8）环烷基，芳基，芳基（C1-4）烷基或NR6R7取代，并且该环可能与苯环融合；R3为（C1-6）烷基，（C3-8）环烷基（可包括来自O、S或NR8的1个或多个杂原子），芳基，芳基（C1-4）烷基或杂芳基；R4为H或（C1-4）烷基；或R3和R4与它们结合的氮一起形成一个4-8元杂环，可进一步包括1个或多个来自O、S或NR9的杂原子；R5、R8和R9独立地为H，（C1-4）烷基，（C3-8）环烷基，芳基或芳基（C1-4）烷基；R6和R7独立地为H或（C1-4）烷基；或R6和R7与它们结合的氮一起形成一个4-8元杂环；或其药学上可接受的盐，用于制备治疗骨质疏松症和动脉粥样硬化的药物。

  公开号：

  WO2005011703A1

文献信息

• SUBSTITUTED 4-AMINO-2-ARYLTETRAHYDROQUINAZOLINES, THEIR PREPARATION, THEIR USE AND PHARMACEUTICAL COMPOSITIONS COMPRISING THEM
  申请人：Aventis Pharma Deutschland GmbH

  公开号：EP1150963A1

  公开（公告）日：2001-11-07
• [EN] SUBSTITUTED 4-AMINO-2-ARYLTETRAHYDROQUINAZOLINES, THEIR PREPARATION, THEIR USE AND PHARMACEUTICAL COMPOSITIONS COMPRISING THEM<br/>[FR] 4-AMINO-2-ARYLTETRAHYDROQUINAZOLINES SUBSTITUEES, PREPARATION ET UTILISATION DE CES DERNIERES, ET COMPOSITIONS PHARMACEUTIQUES LES COMPRENANT
  申请人：AVENTIS PHARMA GMBH

  公开号：WO2000046214A1

  公开（公告）日：2000-08-10

  The present invention relates to compounds of formula (I) in which R?1, R2, and R3¿ have the meanings indicated in the claims, which are valuable pharmaceutical active compounds for the therapy and prophylaxis of diseases, for example of cardiovascular disorders such as high blood pressure, angina pectoris, cardiac insufficiency, thromboses or atherosclerosis. The compounds of formula (I) have the ability to modulate the endogenous production of cyclic guanosine monophosphate (cGMP) and are generally suitable for the therapy and prophylaxis of disease states which are associated with a disturbed cGMP balance. The invention furthermore relates to processes for the preparation of compounds of formula (I), their use for the therapy and prophylaxis of the designated disease states and for the production of pharmaceuticals therefor, and pharmaceutical compositions which comprise a compound of formula (I).
• [EN] 2-CYANO-1,3,5-TRIAZINE-4,6-DIAMINE DERIVATIVES<br/>[FR] DERIVES 2-CYANO-1,3,5-TRIAZINE-4,6-DIAMINES
  申请人：AKZO NOBEL NV

  公开号：WO2005011703A1

  公开（公告）日：2005-02-10

  The invention relates to the use of a 2-cyano-1,3,5-triazine -4,6-diamine derivative having general formula (I), wherein R1 is (C1-6)alkyl, (C3-8)cycloalkyl, aryl, aryl(C1-4)alkyl, aryloxy(C1-4)alkyl, heteroaryl or heteroaryloxy(C1-4)alkyl; R2 is H or (C1-4)alkyl; or R1 and R2 together with the nitrogen to which they are bound form a 4-8 membered heterocyclic ring, optionally further comprising 1 or more heteroatoms selected from O, S or NR5, which ring may be substituted with (C1-4)alkyl, (C3-8)cycloalkyl, aryl, aryl(C1-4)alkyl or NR6R7,and which ring may be fused to a benzene ring; R3 is (C1-6)alkyl, (C3-8) cycloalkyl (optionally comprising 1 or more heteroatoms selected from O, S or NR8), aryl, aryl(C1-4)alkyl or heteroaryl; R4 is H or (C1-4)alkyl; or R3 and R4 together with the nitrogen to which they are bound form a 4-8 membered heterocyclic ring, optionally further comprising 1 or more heteroatoms selected from O, S or NR9; R5, R8 and R9 are independently H, (C1-4)alkyl, (C3-8) cycloalkyl, aryl or aryl(C1-4)alkyl; R6 and R7 are independently H or (C1-4)alkyl; or R6 and R7 form together with the nitrogen to which they are bound a 4-8 membered heterocyclic ring; or a pharmaceutically acceptable salt thereof, for the preparation of a medicament for the treatment of osteoporosis and atherosclerosis.

  该发明涉及使用具有通式（I）的2-氰基-1,3,5-三嗪-4,6-二胺衍生物，其中R1为（C1-6）烷基，（C3-8）环烷基，芳基，芳基（C1-4）烷基，芳氧基（C1-4）烷基，杂芳基或杂芳氧基（C1-4）烷基；R2为H或（C1-4）烷基；或R1和R2与它们结合的氮一起形成一个4-8元杂环，可进一步包括1个或多个来自O、S或NR5的杂原子，该环可能被（C1-4）烷基，（C3-8）环烷基，芳基，芳基（C1-4）烷基或NR6R7取代，并且该环可能与苯环融合；R3为（C1-6）烷基，（C3-8）环烷基（可包括来自O、S或NR8的1个或多个杂原子），芳基，芳基（C1-4）烷基或杂芳基；R4为H或（C1-4）烷基；或R3和R4与它们结合的氮一起形成一个4-8元杂环，可进一步包括1个或多个来自O、S或NR9的杂原子；R5、R8和R9独立地为H，（C1-4）烷基，（C3-8）环烷基，芳基或芳基（C1-4）烷基；R6和R7独立地为H或（C1-4）烷基；或R6和R7与它们结合的氮一起形成一个4-8元杂环；或其药学上可接受的盐，用于制备治疗骨质疏松症和动脉粥样硬化的药物。