(1S,4S)-2-tert-butyl-2,5-diaza-bicyclo[2.2.1]heptane | 861417-79-0

• 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: (1S,4S)-2-tert-butyl-2,5-diaza-bicyclo[2.2.1]heptane
• 英文别名: (1S,4S)-2-tert-butyl-2,5-diazabicyclo[2.2.1]heptane
• CAS: 861417-79-0
• 化学式: C₉H₁₈N₂
• 分子量: 154.255
• InChiKey: FDVWVWGMABVHAS-YUMQZZPRSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  0.9
• 重原子数：
  11
• 可旋转键数：
  1
• 环数：
  2.0
• sp3杂化的碳原子比例：
  1.0
• 拓扑面积：
  15.3
• 氢给体数：
  1
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  (1S,4S)-2-tert-butyl-2,5-diaza-bicyclo[2.2.1]heptane 、 5-chloro-7-(2-chloro-pyridin-4-yl)-imidazo[1,2-c]pyrimidine 在 N,N-二异丙基乙胺 作用下， 以 二氯甲烷 为溶剂， 反应 15.0h， 生成 (S,S)-7-(2-chloro-pyridin-4-yl)-5-(5-tert-butyl-2,5-diaza-bicyclo[2.2.1]hept-2-yl)-imidazo[1,2-c]pyrimidine
  参考文献：
  名称：

  [EN] SUBSTITUTED DIAZABICYCLOHEPTANES AND THEIR USE AS PROTEIN KINASE INHIBITORS
  [FR] DIAZABICYCLOHEPTANES SUBSTITUES ET LEUR UTILISATION COMME INHIBITEURS DE LA PROTEINE KINASE

  摘要：

  本发明涉及治疗性的重氮双环吡啶类化合物及其在治疗关节炎、类风湿关节炎、银屑病性关节炎或骨关节炎、器官移植、急性移植或异种移植和同种移植排斥、缺血再灌注损伤、移植耐受诱导、多发性硬化症、炎症性肠病、溃疡性结肠炎、克罗恩病、狼疮、移植物抗宿主病、T细胞介导的超敏反应疾病、接触性超敏反应、延迟型超敏反应、对麸质敏感性肠病、1型糖尿病、银屑病、接触性皮炎、Hashimoto甲状腺炎、Sjogren综合症、自身免疫性甲状腺功能亢进症、Graves'病、Addison病、自身多腺体疾病、自身性脱发、恶性贫血、白癜风、自身性垂体功能减退症、格林-巴雷综合征、自身免疫疾病、肾小球肾炎、血清病、荨麻疹、呼吸道过敏、哮喘、花粉症、过敏性鼻炎、皮肤过敏、硬皮病、真菌病、急性炎症反应、急性呼吸窘迫综合征、皮肌炎、斑秃、慢性光化性皮炎、湿疹、Behcet病、掌跖症病、脓皮病、塞扎里综合征、特应性皮炎、系统性硬化症、硬皮病、2型糖尿病和PKCθ或其他PKC家族激酶被激活、过度表达或促进肿瘤生长或肿瘤细胞存活、T细胞白血病、胸腺瘤、T和B细胞淋巴瘤、结肠癌、乳腺癌和肺癌或对化疗药物具有抗性的治疗中的应用。

  公开号：

  WO2005070934A1
• 作为产物：
  描述：

  (1S,4S)-5-tert-butyl-2,5-diaza-bicyclo[2.2.1]heptane-2-carboxylic acid tert-butyl ester 在 盐酸 、 甲醇 作用下， 以 1,4-二氧六环 为溶剂， 反应 1.0h， 生成 (1S,4S)-2-tert-butyl-2,5-diaza-bicyclo[2.2.1]heptane
  参考文献：
  名称：

  [EN] SUBSTITUTED DIAZABICYCLOHEPTANES AND THEIR USE AS PROTEIN KINASE INHIBITORS
  [FR] DIAZABICYCLOHEPTANES SUBSTITUES ET LEUR UTILISATION COMME INHIBITEURS DE LA PROTEINE KINASE

  摘要：

  本发明涉及治疗性的重氮双环吡啶类化合物及其在治疗关节炎、类风湿关节炎、银屑病性关节炎或骨关节炎、器官移植、急性移植或异种移植和同种移植排斥、缺血再灌注损伤、移植耐受诱导、多发性硬化症、炎症性肠病、溃疡性结肠炎、克罗恩病、狼疮、移植物抗宿主病、T细胞介导的超敏反应疾病、接触性超敏反应、延迟型超敏反应、对麸质敏感性肠病、1型糖尿病、银屑病、接触性皮炎、Hashimoto甲状腺炎、Sjogren综合症、自身免疫性甲状腺功能亢进症、Graves'病、Addison病、自身多腺体疾病、自身性脱发、恶性贫血、白癜风、自身性垂体功能减退症、格林-巴雷综合征、自身免疫疾病、肾小球肾炎、血清病、荨麻疹、呼吸道过敏、哮喘、花粉症、过敏性鼻炎、皮肤过敏、硬皮病、真菌病、急性炎症反应、急性呼吸窘迫综合征、皮肌炎、斑秃、慢性光化性皮炎、湿疹、Behcet病、掌跖症病、脓皮病、塞扎里综合征、特应性皮炎、系统性硬化症、硬皮病、2型糖尿病和PKCθ或其他PKC家族激酶被激活、过度表达或促进肿瘤生长或肿瘤细胞存活、T细胞白血病、胸腺瘤、T和B细胞淋巴瘤、结肠癌、乳腺癌和肺癌或对化疗药物具有抗性的治疗中的应用。

  公开号：

  WO2005070934A1

文献信息

• Dual Pharmacophores - PDE4-Muscarinic Antagonistics
  申请人：Callahan James Francis

  公开号：US20090197871A1

  公开（公告）日：2009-08-06

  The present invention is directed to novel compounds of Formula (I), pharmaceutical compositions and their use in therapy, for example as inhibitors of phosphodiesterase type IV (PDE4) and as antagonists of muscarinic acetylcholine receptors (mAChRs), in the treatment of/and or prophylaxis of respiratory diseases, including antiinflammatory and/or allergic diseases such as chronic obstructive pulmonary disease (COPD), asthma, rhinitis (e.g. allergic rhinitis), atopic dermatitis or psoriasis.

  本发明涉及式(I)的新化合物，药物组合物及其在治疗中的应用，例如作为磷酸二酯酶IV (PDE4)的抑制剂和毒蕈碱乙酰胆碱受体 (mAChRs)的拮抗剂，用于治疗和/或预防呼吸道疾病，包括抗炎症和/或过敏性疾病，如慢性阻塞性肺病 (COPD)、哮喘、鼻炎 (例如过敏性鼻炎)、特应性皮炎或银屑病。
• [EN] PYRROLOPYRIMIDINE COMPOUNDS AS INHIBITORS OF CDK4/6<br/>[FR] COMPOSÉS DE LA PYRROLOPYRIMIDINE UTILISÉS EN TANT QU'INHIBITEURS DES CDK4/6
  申请人：NOVARTIS AG

  公开号：WO2011101409A1

  公开（公告）日：2011-08-25

  The invention is directed to novel pyrrolopyrimidine compounds of formula (I) wherein R1, R2Y, R4, R8- R11, A and L are defined herein and to salts, including pharmaceutically acceptable salts thereof. The compounds of the present invention are CDK4/6 inhibitors and could be useful in the treatment of diseases and disorders mediated by CDK4/6, such as cancer, including mantle cell lymphoma, liposarcoma, non small cell lung cancer, melanoma, squamous cell esophageal cancer and breast cancer. The invention is further directed to pharmaceutical compositions comprising a compound of the invention. The invention is still further directed to methods of inhibiting CDK4/6 activity and to the treatment of disorders associated therewith using a compound of the invention or a pharmaceutical composition comprising a compound of the invention.

  本发明涉及一种新型吡咯吡嘧啶化合物，其化学式为（I），其中R1、R2Y、R4、R8-R11、A和L的定义如下，以及其盐，包括其药用可接受盐。本发明的化合物是CDK4/6抑制剂，可用于治疗由CDK4/6介导的疾病和紊乱，如癌症，包括袍细胞淋巴瘤、脂肪肉瘤、非小细胞肺癌、黑色素瘤、鳞状细胞食管癌和乳腺癌。本发明还涉及包含本发明化合物的药物组合物。此外，本发明还涉及通过使用本发明化合物或包含本发明化合物的药物组合物来抑制CDK4/6活性和治疗相关疾病的方法。
• Pyridine [3,4-b] Pyrazinones
  申请人：Hughes O. Robert

  公开号：US20070249615A1

  公开（公告）日：2007-10-25

  Compounds and pharmaceutically acceptable salts of the compounds are disclosed, wherein the compounds have the structure of Formula I: wherein R 2 , R 6A , R 6B and R 8 are as defined in the specification. Corresponding pharmaceutical compositions, methods of treatment, synthetic methods, and intermediates are also disclosed.

  本文披露了化合物及其药用可接受的盐，其中化合物具有以下结构的Formula I：其中R2、R6A、R6B和R8如规范中定义。同时还披露了相应的药物组合物、治疗方法、合成方法和中间体。
• Substituted heterocyclic compounds and methods of use
  申请人：Cao Guo-Qiang

  公开号：US20050182072A1

  公开（公告）日：2005-08-18

  The present invention relates to therapeutic diazobicyclo pyridines and their use in the treatment of arthritis, rheumatoid arthritis, psoriatic arthritis or osteoarthritis, organ transplant, acute transplant or heterograft and homograft rejection, ischemic and reperfusion injury, transplantation tolerance induction, multiple sclerosis, inflammatory bowel disease, ulcerative colitis, Crohn's disease, lupus, graft vs. host diseases, T -cell mediated hypersensitivity diseases, contact hypersensitivity, delayed-type hypersensitivity, gluten-sensitive enteropathy, Type 1 diabetes, psoriasis, contact dermatitis, Hashimoto's thyroiditis, Sjogren's syndrome, autoimmune hyperthyroidism, Graves' Disease, Addison's disease, autoimmune polyglandular disease, autoimmune alopecia, pernicious anemia, vitiligo, autoimmune hypopituatarism, Guillain-Barre syndrome, autoimmune diseases, glomerulonephritis, serum sickness, uticaria, respiratory allergies, asthma, hayfever, allergic rhinitis, skin allergies, scleracielma, mycosis flugoides, acute inflammatory responses, acute respiratory distress syndrome, dermatomyositis, alopecia areata, chronic actinic dermatitis, eczema, Behcet's disease, Pustulosis palmoplanteris, Pyoderma gangrenum, Sezary's syndrome, atopic dermatitis, systemic schlerosis, morphea, Type II diabetes and cancers where PKC theta or other PKC-family kinases are activated, overexpressed or facilitate tumor growth or survival of tumor cells, T cell leukemia, thymoma, T and B cell lymphoma, colon carcinoma, breast carcinoma and lung carcinoma or provides resistance to chemotherapeutic drugs.

  本发明涉及治疗用的二氮杂双环吡啶及其在治疗关节炎、类风湿性关节炎、银屑病性关节炎或骨关节炎、器官移植、急性移植或异种移植和同种移植排斥、缺血再灌注损伤、移植耐受诱导、多发性硬化症、炎症性肠病、溃疡性结肠炎、克罗恩病、红斑狼疮、移植物抗宿主病、T细胞介导的超敏反应性疾病、接触性超敏反应、迟发型超敏反应、麦糊疹性肠病、1型糖尿病、银屑病、接触性皮炎、桥本甲状腺炎、干燥综合症、自身免疫性甲状腺功能亢进症、格雷夫斯病、亚当逊病、自身免疫性多发性内分泌腺疾病、自身免疫性脱发症、恶性贫血、白癜风、自身免疫性下丘脑功能减退症、格林-巴利综合症、自身免疫性疾病、肾小球肾炎、血清病、荨麻疹、呼吸道过敏、哮喘、花粉热、过敏性鼻炎、皮肤过敏、硬皮病、浆液性腺瘤、急性炎症反应、急性呼吸窘迫综合症、皮肌炎、斑秃、慢性光化性皮炎、湿疹、Behcet病、掌跖角化症、脓疱性荨麻疹、Sezary综合症、特应性皮炎、系统性硬化病、硬皮症、2型糖尿病和PKC theta或其他PKC家族激酶被激活、过度表达或促进肿瘤生长或肿瘤细胞存活、T细胞白血病、胸腺瘤、T和B细胞淋巴瘤、结肠癌、乳腺癌和肺癌或提供对化疗药物的抗性。
• Acylated piperidine derivatives as melanocortin-4 receptor modulators
  申请人：Bakshi Raman K.

  公开号：US20090253744A1

  公开（公告）日：2009-10-08

  Certain novel N-acylated spiropiperidine derivatives are ligands of the human melanocortin receptor(s) and, in particular, are selective ligands of the human melanocortin-4 receptor (MC-4R). They are therefore useful for the treatment, control, or prevention of diseases and disorders responsive to the modulation of MC-4R, such as obesity, diabetes, nicotine addiction, alcoholism, sexual dysfunction, including erectile dysfunction and female sexual dysfunction.

  某些新型N-酰化的螺环吡啶衍生物是人类黑色素细胞素受体的配体，特别是人类黑色素细胞素-4受体（MC-4R）的选择性配体。因此，它们可用于治疗、控制或预防对MC-4R调节敏感的疾病和障碍，如肥胖症、糖尿病、尼古丁成瘾、酗酒、性功能障碍，包括勃起功能障碍和女性性功能障碍。