4-cyclopentyl-3-(trifluoromethyl)benzoic acid | 952511-63-6

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: 4-cyclopentyl-3-(trifluoromethyl)benzoic acid
• 英文别名: 4-Cyclopentyl-3-trifluoromethyl-benzoic acid
• CAS: 952511-63-6
• 化学式: C₁₃H₁₃F₃O₂
• 分子量: 258.24
• InChiKey: YIXUTIVJXCNQMQ-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.3
• 重原子数：
  18
• 可旋转键数：
  2
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.46
• 拓扑面积：
  37.3
• 氢给体数：
  1
• 氢受体数：
  5

反应信息

• 作为反应物：
  描述：

  4-cyclopentyl-3-(trifluoromethyl)benzoic acid 在 N,N-二甲基甲酰胺 N-氯代丁二酰亚胺 、 草酰氯 、 三乙胺 作用下， 以 四氢呋喃 、 二氯甲烷 、 N,N-二甲基甲酰胺 为溶剂， 反应 19.0h， 生成 tert-butyl 2-(9-chloro-7-(5-(4-cyclopentyl-3-(trifluoromethyl)phenyl)-1,2,4-oxadiazol-3-yl)-2,3-dihydro-1H-pyrrolo[1,2-a]indol-1-yl)acetate
  参考文献：
  名称：

  [EN] DISUBSTITUTED OXADIAZOLE DERIVATIVES USEFUL IN THE TREATMENT OF AUTOIMMUNE AND INFLAMMATORY DISORDERS
  [FR] DÉRIVÉS D'OXADIAZOLE DISUBSTITUÉS UTILES DANS LE TRAITEMENT DE TROUBLES AUTO-IMMUNS ET INFLAMMATOIRES

  摘要：

  本发明涉及Formula (Ia)的某些二取代噁二唑衍生物及其药用可接受的盐、溶剂化合物和水合物，这些化合物展示出有用的药理特性，例如作为S1P1受体激动剂。本发明还提供了含有本发明化合物的药物组合物，以及使用本发明化合物和组合物治疗S1P1相关疾病的方法，例如牛皮癣、类风湿关节炎、克罗恩病、移植排斥、多发性硬化症、全身性红斑狼疮、溃疡性结肠炎、I型糖尿病、痤疮、心肌缺血再灌注损伤、高血压性肾病、肾小球硬化、胃炎、多发性肌炎、甲状腺炎、白癜风、肝炎、胆管肝硬化、微生物感染及相关疾病、病毒感染及相关疾病、淋巴细胞介导的疾病和疾病、自身免疫疾病、炎症性疾病和癌症。

  公开号：

  WO2011005290A1
• 作为产物：
  描述：

  环戊烯-1-基硼酸 在 (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride 、 palladium 10% on activated carbon 、 氢气 、 potassium carbonate 作用下， 以 甲醇 、 正丁醇 为溶剂， 50.0~100.0 ℃ 、1.0 MPa 条件下， 反应 28.0h， 生成 4-cyclopentyl-3-(trifluoromethyl)benzoic acid
  参考文献：
  名称：

  BENZO 2-AZASPIRO[4.4]NONANE COMPOUND AND USE THEREOF

  摘要：

  本发明公开了一系列的苯并-2-氮杂二环[4.4]壬烷化合物，具体而言，公开了一种如式(P)所示的化合物或其药学上可接受的盐。

  公开号：

  EP4116294A1

文献信息

• [EN] PROCESSES FOR THE PREPARATION OF (R)-2-(7-(4-CYCLOPENTYL-3-(TRIFLUOROMETHYL)BENZYLOXY)-1,2,3,4-TETRAHYDROCYCLOPENTA[B]INDOL-3-YL)ACETIC ACID AND SALTS THEREOF<br/>[FR] PROCÉDÉS DE PRÉPARATION D'ACIDE (R)-2-(7-(4-CYCLOPENTYL-3-(TRIFLUOROMÉTHYL)BENZYLOXY)-1,2,3,4-TÉTRAHYDROCYCLOPENTA]INDOL-3-YL) ACÉTIQUE ET DE SES SELS
  申请人：ARENA PHARM INC

  公开号：WO2011094008A1

  公开（公告）日：2011-08-04

  The present invention relates to processes and intermediates useful in the preparation of of (R)-2-(7-(4-cyclopentyl-3-(trifluoromethyl)benzyloxy)-1,2,3,4-tetrahydrocyclopenta[b]indol-3-yl)acetic acid of Formula (Ia) and salts thereof, an S1P1 receptor modulator that is useful in the treatment of S1P1 receptor-associated disorders, for example, diseases and disorders mediated by lymphocytes, transplant rejection, autoimmune diseases and disorders, inflammatory diseases and disorders (e.g., acute and chronic inflammatory conditions), cancer, and conditions characterized by an underlying defect in vascular integrity or that are associated with angiogenesis such as may be pathologic (e.g., as may occur in inflammation, tumor development and atherosclerosis).

  本发明涉及用于制备（R）-2-(7-(4-环戊基-3-(三氟甲基)苄氧基)-1,2,3,4-四氢环戊[b]吲哚-3-基)乙酸及其盐的过程和中间体，该化合物是S1P1受体调节剂，用于治疗S1P1受体相关疾病，例如由淋巴细胞介导的疾病和疾病，移植排斥反应，自身免疫疾病和疾病，炎症性疾病和疾病（例如，急性和慢性炎症症状），癌症，以及具有血管完整性基础缺陷或与血管生成相关的疾病和疾病，如可能是病理性的（例如，在炎症、肿瘤发展和动脉粥样硬化中可能发生的情况）。
• HETEROARYLAMIDE LOWER CARBOXYLIC ACID DERIVATIVE
  申请人：Machinaga Nobuo

  公开号：US20090324581A1

  公开（公告）日：2009-12-31

  To provide a novel compound which has S1P receptor agonistic activity, exhibits excellent immunosuppressing effect, gives less adverse side effects, and can be orally administered. The invention provides a compound represented by general formula (I) (wherein A is a single bond, —O—, or —CH 2 —; R 1 represents a hydrogen atom or a C 1 -C 6 alkyl group, and V represents any one group selected from among the following groups (1) to (3): (1) -G 1 -, (2) -G 2 -N(R 2 )-G 3 -, and (3) a group represented by formula 2, wherein each of Z 1 and Z 2 represents a hydrogen atom or a C 1 -C 6 alkyl group, Z 3 represents a hydrogen or the like, Q represents —CH 2 —O— or the like, and Y represents a group represented by formula 3, a salt thereof, or a solvate thereof.

  提供一种新型化合物，具有S1P受体激动活性，表现出优异的免疫抑制效果，产生较少的不良副作用，并可口服。本发明提供一种由通式（I）表示的化合物（其中A是单键，-O-或-CH2-；R1表示氢原子或C1-C6烷基基团，V表示从以下组（1）至（3）中选择的任一组：（1）-G1-，（2）-G2-N（R2）-G3-，以及（3）由式2表示的组，其中Z1和Z2分别表示氢原子或C1-C6烷基基团，Z3表示氢或类似物，Q表示- -O-或类似物，Y表示由式3表示的基团，其盐或溶剂化物。
• HETERO COMPOUND
  申请人：HARADA Hironori

  公开号：US20090076070A1

  公开（公告）日：2009-03-19

  [Problems] To provide a useful compound as an active ingredient for a preventing and/or treating agent for rejection in the transplantation of an organ, bone marrow, or a tissue, an autoimmune disease, or the like, which has an excellent S1P 1 agonist activity. [Means for Solving] Since the compound of the invention has an S1P 1 agonist activity, it is useful as an active ingredient for a treating or preventing agent for a disease caused by unfavorable lymphocytic infiltration, for example, an autoimmune disease such as graft rejection in the transplantation of an organ, bone marrow, or a tissue, a graft-versus-host disease, rheumatic arthritis, multiple sclerosis, systemic lupus erythematosus, a nephrotic syndrome, encephalomeningitis, myasthenia gravis, pancreatitis, hepatitis, nephritis, diabetes, pulmonary disorder, asthma, atopic dermatitis, inflammatory bowel disease, atherosclerosis, ischemia-reperfusion injury, or an inflammatory disease, and further, a disease caused by the abnormal growth or accumulation of cells such as cancer and leukemia.

  [问题] 提供一种有优异S1P1激动剂活性的化合物，作为器官、骨髓或组织移植、自身免疫性疾病等引起的排异的预防和/或治疗剂的有效活性成分。 [解决方法] 由于本发明的化合物具有S1P1激动剂活性，因此可用作治疗或预防由不良淋巴细胞浸润引起的疾病的活性成分，例如器官、骨髓或组织移植的移植排斥、移植物抗宿主病、风湿性关节炎、多发性硬化症、全身性红斑狼疮、肾病综合症、脑脊髓炎、重症肌无力、胰腺炎、肝炎、肾炎、糖尿病、肺部疾病、哮喘、特应性皮炎、炎症性肠病、动脉粥样硬化、缺血再灌注损伤或异常细胞生长或积累引起的癌症和白血病等疾病。
• 2H-CHROMENE COMPOUND AND DERIVATIVE THEREOF
  申请人：Harada Hironori

  公开号：US20120178735A1

  公开（公告）日：2012-07-12

  Provided is a 2H-chromene compound or a derivative thereof which has an excellent S1P1 agonist action. The 2H-chromene compound or derivative is particularly useful for preventing and/or treating a disease induced by undesirable lymphocyte infiltration or a disease induced by abnormal proliferation or accumulation of cells.

  提供了一种2H-色烯化合物或其衍生物，具有优异的S1P1激动剂作用。该2H-色烯化合物或衍生物特别适用于预防和/或治疗由不良淋巴细胞浸润引起的疾病或由细胞异常增殖或堆积引起的疾病。
• PROCESSES FOR THE PREPARATION OF (R)-2-(7-(4-CYCLOPENTYL-3-(TRIFLUOROMETHYL)BENZYLOXY)-1,2,3,4-TETRAHYDROCYCLOPENTA[B]INDOL-3-YL)ACETIC ACID AND SALTS THEREOF
  申请人：Montalban Antonio Garrido

  公开号：US20120295947A1

  公开（公告）日：2012-11-22

  The present invention relates to processes and intermediates useful in the preparation of (R)-2-(7-(4-cyclopentyl-3-(trifluoromethyl)benzyloxy)-1,2,3,4-tetrahydrocyclopenta[b]indol-3-yl)acetic acid of Formula (Ia) and salts thereof, an S1P1 receptor modulator that is useful in the treatment of S1P1 receptor-associated disorders, for example, diseases and disorders mediated by lymphocytes, transplant rejection, autoimmune diseases and disorders, inflammatory diseases and disorders (e.g., acute and chronic inflammatory conditions), cancer, and conditions characterized by an underlying defect in vascular integrity or that are associated with angiogenesis such as may be pathologic (e.g., as may occur in inflammation, tumor development and atherosclerosis).

  本发明涉及用于制备(R)-2-(7-(4-环戊基-3-(三氟甲基)苯基氧基)-1,2,3,4-四氢环戊[b]吲哚-3-基)乙酸及其盐的过程和中间体，它是一种S1P1受体调节剂，可用于治疗S1P1受体相关疾病，例如淋巴细胞介导的疾病和疾病，移植排斥反应，自身免疫性疾病和疾病，炎症性疾病和疾病（例如急性和慢性炎症状况），癌症以及以血管完整性缺陷为基础或与血管生成相关的病症，如可能是病理性的（例如可能发生在炎症，肿瘤发展和动脉粥样硬化中）。