tert-butyl 3-(5-methyl-7H-pyrrolo [2,3-d]pyrimidin-4-yl)-3,8-diazabicyclo[3.2.1]octane-8-carboxylate | 1116570-98-9

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 二嗪烷类
• 英文名称: tert-butyl 3-(5-methyl-7H-pyrrolo [2,3-d]pyrimidin-4-yl)-3,8-diazabicyclo[3.2.1]octane-8-carboxylate
• 英文别名: tert-butyl 3-(5-methyl-7H-pyrrolo[2,3-d]pyrimidin-4-yl)-3,8-diazabicyclo[3.2.1]octane-8-carboxylate
• CAS: 1116570-98-9
• 化学式: C₁₈H₂₅N₅O₂
• 分子量: 343.429
• InChiKey: NBXXAIGGOFKPEW-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.8
• 重原子数：
  25
• 可旋转键数：
  3
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.61
• 拓扑面积：
  74.4
• 氢给体数：
  1
• 氢受体数：
  5

反应信息

• 作为反应物：
  描述：

  tert-butyl 3-(5-methyl-7H-pyrrolo [2,3-d]pyrimidin-4-yl)-3,8-diazabicyclo[3.2.1]octane-8-carboxylate 在 盐酸 作用下， 以 1,4-二氧六环 为溶剂， 反应 1.0h， 以91%的产率得到4-(3,8-diazabicyclo[3.2.1]octan-3-yl)-5-methyl-7H-pyrrolo[2,3-d]pyrimidine dihydrochloride
  参考文献：
  名称：

  KINASE INHIBITORS, COMPOSITIONS COMPRISING THEM, AND METHODS OF THEIR USE

  摘要：

  抑制LIM激酶2的抑制剂已被披露，以及包含它们的药物组合物和使用方法。

  公开号：

  US20090042893A1
• 作为产物：
  描述：

  4-氯-5-甲基-7H-吡咯并[2,3-d]嘧啶 、 8-BOC-3,8-二氮杂双环[3.2.1]辛烷 在 三乙胺 作用下， 以 异丙醇 为溶剂， 反应 0.5h， 以66%的产率得到tert-butyl 3-(5-methyl-7H-pyrrolo [2,3-d]pyrimidin-4-yl)-3,8-diazabicyclo[3.2.1]octane-8-carboxylate
  参考文献：
  名称：

  KINASE INHIBITORS, COMPOSITIONS COMPRISING THEM, AND METHODS OF THEIR USE

  摘要：

  抑制LIM激酶2的抑制剂已被披露，以及包含它们的药物组合物和使用方法。

  公开号：

  US20090042893A1

文献信息

• [EN] HETEROCYCLIC COMPOUNDS AS JAK RECEPTOR AND PROTEIN TYROSINE KINASE INHIBITORS<br/>[FR] COMPOSÉS HÉTÉROCYCLIQUES EN TANT QU’INHIBITEURS DU RÉCEPTEUR JAK ET DE LA PROTÉINE TYROSINE KINASE
  申请人：LEO PHARMA AS

  公开号：WO2011003418A1

  公开（公告）日：2011-01-13

  The invention relates to compounds of general formula (I) wherein A, R1, R2, R3, R4, R5, R9, m and n are defined as defined herein, and pharmaceutically acceptable salts, hydrates, or solvates thereof, for use -alone or in combination with one or more other pharmaceutically active compounds- in therapy, as JAK kinase and protein tyrosine kinase inhibitors for preventing, treating or ameliorating diseases and complications thereof, including, for example, psoriasis, atopic dermatitis, rosacea, lupus, multiple sclerosis, rheumatoid arthritis, Type I diabetes, asthma, cancer, autoimmune thyroid disorders, ulcerative colitis, Crohn's disesase, Alzheimer's disease, leukaemia, eye diseases such as diabetic retinopathy and macular degeneration as well as other autoimmune diseases and indications where immunosuppression would be desirable for example in organ transplantation.

  该发明涉及通用式（I）的化合物，其中A，R1，R2，R3，R4，R5，R9，m和n如本文所定义，以及其在治疗中的药用盐、水合物或溶剂合物，可单独使用或与一个或多个其他药用活性化合物结合使用，作为JAK激酶和蛋白酪氨酸激酶抑制剂，用于预防、治疗或改善疾病及其并发症，包括例如牛皮癣、特应性皮炎、酒渣鼻、红斑狼疮、多发性硬化、类风湿关节炎、I型糖尿病、哮喘、癌症、自身免疫性甲状腺疾病、溃疡性结肠炎、克罗恩病、阿尔茨海默病、白血病、眼疾如糖尿病视网膜病变和黄斑变性，以及其他自身免疫疾病和需要免疫抑制的适应症，例如器官移植中。
• HETEROCYCLIC COMPOUNDS AS JAK RECEPTOR AND PROTEIN TYROSINE KINASE INHIBITORS
  申请人：Nielsen Simon Feldbæk

  公开号：US20120178740A1

  公开（公告）日：2012-07-12

  The invention relates to compounds of general formula (I) wherein A, R 1 , R 2 , R 3 , R 4 , R 5 , R 9 , m and n are defined as defined herein, and pharmaceutically acceptable salts, hydrates, or solvates thereof, for use—alone or in combination with one or more other pharmaceutically active compounds—in therapy, as JAK kinase and protein tyrosine kinase inhibitors for preventing, treating or ameliorating diseases and complications thereof, including, for example, psoriasis, atopic dermatitis, rosacea, lupus, multiple sclerosis, rheumatoid arthritis, Type I diabetes, asthma, cancer, autoimmune thyroid disorders, ulcerative colitis, Crohn's disease, Alzheimer's disease, leukaemia, eye diseases such as diabetic retinopathy and macular degeneration as well as other autoimmune diseases and indications where immunosuppression would be desirable for example in organ transplantation.

  本发明涉及通式（I）化合物，其中A，R1，R2，R3，R4，R5，R9，m和n如本说明书所定义，并且其药学上可接受的盐，水合物或溶剂化物，在治疗中使用 - 单独或与一个或多个其他药学活性化合物结合使用 - 作为JAK激酶和蛋白酪氨酸激酶抑制剂，用于预防，治疗或改善疾病及其并发症，包括例如银屑病，特应性皮炎，酒渣鼻，狼疮，多发性硬化症，类风湿性关节炎，1型糖尿病，哮喘，癌症，自身免疫性甲状腺疾病，溃疡性结肠炎，克罗恩病，阿尔茨海默病，白血病，眼部疾病例如糖尿病视网膜病变和黄斑变性以及其他自身免疫性疾病和需要免疫抑制的适应症，例如器官移植。
• Substituted pyrrolo[2,3-d]pyrimidines as LIM kinase 2 inhibitors
  申请人：Harrison Bryce Alden

  公开号：US08507672B2

  公开（公告）日：2013-08-13

  Substituted pyrrolo[2,3-d]pyrimidine-based compounds useful as inhibitors of LIM kinase 2 are disclosed. Also disclosed are pharmaceutical compositions comprising the compounds and methods of their use to treat, manage and prevent inflammatory diseases and disorders, cancer, and diseases and disorders of the eye.

  本发明揭示了一种基于替代吡咯并[2,3-d]嘧啶的化合物，可作为LIM激酶2的抑制剂。还揭示了包含这些化合物的药物组合物以及它们的使用方法，用于治疗、管理和预防炎症性疾病和障碍、癌症以及眼部疾病和障碍。
• (7H-PYRROLO [2, 3-D] PYRIMIDIN-4-YL) -PIPERAZINES AS KINASE INHIBITORS FOR THE TREATMENT OF CANCER AND INFLAMMATION
  申请人：Lexicon Pharmaceuticals, Inc.

  公开号：EP2597098A1

  公开（公告）日：2013-05-29

  Inhibitors of LIM kinase 2 of the following formula are disclosed, along with pharmaceutical compositions comprising them and methods of their use, in particular for treatment of inflammatory and cancerous and ocular diseases. X is O or NRA; A is cycloalkyl, aryl or heterocyclyl; RA is hydrogen, cyano, nitro, RA1, SO2RA1 or SO2N(RA1)2; each RB is independently hydrogen or alkyl. The other variables are as defined in the claims.

  本研究公开了下式的 LIM 激酶 2 抑制剂，以及包含这些抑制剂的药物组合物和使用方法，尤其是用于治疗炎症、癌症和眼部疾病的方法。 X 是 O 或 NRA； A 是环烷基、芳基或杂环基； RA 是氢、氰基、硝基、RA1、SO2RA1 或 SO2N(RA1)2 每个 RB 独立地为氢或烷基。 其他变量如权利要求中所定义。
• (7H-PYRROLO[2,3-D]PYRIMIDIN-4-YL)-PIPERAZINES AS KINASE INHIBITORS FOR THE TREATMENT OF CANCER AND INFLAMMATION
  申请人：Lexicon Pharmaceuticals, Inc.

  公开号：EP2188289B1

  公开（公告）日：2015-10-28