3-(5-bromoisoquinolin-1-yl)quinoline | 919786-57-5

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 吡啶及其衍生物
• 英文名称: 3-(5-bromoisoquinolin-1-yl)quinoline
• 英文别名: 3-(5-Bromoisoquinolin-1-yl)quinoline；5-bromo-1-quinolin-3-ylisoquinoline
• CAS: 919786-57-5
• 化学式: C₁₈H₁₁BrN₂
• 分子量: 335.203
• InChiKey: NJWWXKQEEWPTRN-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.7
• 重原子数：
  21
• 可旋转键数：
  1
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.0
• 拓扑面积：
  25.8
• 氢给体数：
  0
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  喹啉-3-硼酸 、 3-(5-bromoisoquinolin-1-yl)quinoline 、 4-cyano-3-(4-hydroxycyclohexylamino)phenylboronic acid pinacol ester 以A compound of Comparative Example 1 was obtained as a pale yellow solid (yield based on 3 steps: 24%)的产率得到2-(4-hydroxycyclohexylamino)-4-(1-(quinolin-3-yl)isoquinolin-5-yl)benzamide
  参考文献：
  名称：

  Bicyclic compound or salt thereof

  摘要：

  一种具有HSP90抑制作用和抗癌作用的新型双环化合物。基于HSP90抑制作用的制药剂，可用于预防和/或治疗涉及HSP90的疾病，特别是癌症。该化合物具有一般式(I)或其盐，其中X1、X2、X3和X4中至少有一个代表N或N-氧化物，其余各自独立地为C—R2；Y1、Y2、Y3和Y4中的任意一个或两个代表C—R4，其余各自独立地为CH或N；R1代表具有1到4个异原子（选自N、S和O）的可选取代单环或双环不饱和杂环基；R2代表氢原子、具有1到6个碳原子的可选取代烷基等；R3代表氢原子、—CO—R5等。

  公开号：

  US08912181B2

文献信息

• NOVEL BICYCLIC COMPOUND OR SALT THEREOF
  申请人：Kitade Makoto

  公开号：US20130296320A1

  公开（公告）日：2013-11-07

  Provided is a novel bicyclic compound which has an HSP90 inhibitory effect and a carcinostatic effect. Also provided is a pharmaceutical agent which is based on the HSP90 inhibitory effect and is useful in the prevention and/or treatment of a disease involving HSP90, particularly, cancer. The present invention provides a compound represented by the following general formula (I) or a salt thereof wherein at least one of X 1 , X 2 , X 3 , and X 4 represents N or N-oxide and the rest thereof are the same or different and each represent C—R 2 ; any one or two of Y 1 , Y 2 , Y 3 , and Y 4 represent C—R 4 and the rest thereof are the same or different and each represent CH or N; R 1 represents an optionally substituted monocyclic or bicyclic unsaturated heterocyclic group having 1 to 4 heteroatoms selected from N, S, and O; R 2 represents a hydrogen atom, an optionally substituted alkyl group having 1 to 6 carbon atoms etc.; R 3 represents a hydrogen atom, —CO—R 5 etc.; R 4 represents a hydrogen atom, —CO—R 6 , —N(R 7 )(R 8 ) etc.; R 5 represents a hydroxyl group, an amino group etc.; R 6 represents a hydroxyl group etc.; R 7 and R 8 are the same or different and each represent a hydrogen atom, an optionally substituted alkyl group having 1 to 6 carbon atoms etc.; and R 9 represents an optionally substituted cycloalkyl group having 3 to 7 carbon atoms etc.

  提供了一种新颖的双环化合物，具有HSP90抑制作用和抗癌作用。还提供了一种基于HSP90抑制作用的药物剂，用于预防和/或治疗涉及HSP90的疾病，特别是癌症。本发明提供了以下一般式(I)所表示的化合物或其盐，其中X1、X2、X3和X4中的至少一个代表N或N-氧化物，其余部分相同或不同，每个代表C—R2；Y1、Y2、Y3和Y4中的任意一个或两个代表C—R4，其余部分相同或不同，每个代表CH或N；R1代表具有1至4个异原子（N、S和O）的可选择取代的单环或双环不饱和杂环基；R2代表氢原子、具有1至6个碳原子的可选择取代的烷基基团等；R3代表氢原子、—CO—R5等；R4代表氢原子、—CO—R6、—N(R7)(R8)等；R5代表羟基、氨基等；R6代表羟基等；R7和R8相同或不同，每个代表氢原子、具有1至6个碳原子的可选择取代的烷基基团等；R9代表具有3至7个碳原子的可选择取代的环烷基基团等。
• BICYCLIC COMPOUNDS OR SALTS THEREOF FOR USE IN THE TREATMENT OF CANCER
  申请人：Taiho Pharmaceutical Co., Ltd.

  公开号：EP2662357B1

  公开（公告）日：2016-08-03
• US8912181B2
  申请人：——

  公开号：US8912181B2

  公开（公告）日：2014-12-16
• Bicyclic compound or salt thereof
  申请人：Kitade Makoto

  公开号：US08912181B2

  公开（公告）日：2014-12-16

  A novel bicyclic compound having an HSP90 inhibitory effect and a carcinostatic effect. A pharmaceutical agent based on the HSP90 inhibitory effect and useful in the prevention and/or treatment of a disease involving HSP90, particularly cancer. The compound has a general formula (I) or is a salt thereof wherein at least one of X1, X2, X3, and X4 represents N or N-oxide and the rest thereof are each independently C—R2; any one or two of Y1, Y2, Y3, and Y4 represent C—R4 and the rest thereof are each independently CH or N; R1 represents an optionally substituted monocyclic or bicyclic unsaturated heterocyclic group having 1 to 4 heteroatoms selected from N, S, and O; R2 represents a hydrogen atom, an optionally substituted alkyl group having 1 to 6 carbon atoms etc.; R3 represents a hydrogen atom, —CO—R5 etc.

  一种具有HSP90抑制作用和抗癌作用的新型双环化合物。基于HSP90抑制作用的制药剂，可用于预防和/或治疗涉及HSP90的疾病，特别是癌症。该化合物具有一般式(I)或其盐，其中X1、X2、X3和X4中至少有一个代表N或N-氧化物，其余各自独立地为C—R2；Y1、Y2、Y3和Y4中的任意一个或两个代表C—R4，其余各自独立地为CH或N；R1代表具有1到4个异原子（选自N、S和O）的可选取代单环或双环不饱和杂环基；R2代表氢原子、具有1到6个碳原子的可选取代烷基等；R3代表氢原子、—CO—R5等。