(2-bromo-4-chlorophenyl)hydrazine | 299165-75-6

• 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: (2-bromo-4-chlorophenyl)hydrazine
• 英文别名: (2-bromo-4-chloro-phenyl)-hydrazine；(2-Brom-4-chlor-phenyl)-hydrazin
• CAS: 299165-75-6
• 化学式: C₆H₆BrClN₂
• 分子量: 221.484
• InChiKey: OJMHGYZZACDGPA-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.5
• 重原子数：
  10
• 可旋转键数：
  1
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.0
• 拓扑面积：
  38
• 氢给体数：
  2
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  (2-bromo-4-chlorophenyl)hydrazine 在 盐酸 、 氨 作用下， 以 乙醇 、 水 为溶剂， 反应 47.0h， 生成 methyl 1-(2-bromo-4-chlorophenyl)-1H-pyrazole-5-carboxylate
  参考文献：
  名称：

  [EN] INHIBITORS OF COMPLEMENT FACTORS AND USES THEREOF
  [FR] INHIBITEURS DE FACTEURS DU COMPLÉMENT ET UTILISATIONS ASSOCIÉES

  摘要：

  Disclosed are compounds of formula I and II and pharmaceutically acceptable salts thereof. Also disclosed are methods of treating a neurodegenerative disorder, an inflammatory disease, an autoimmune disease, an ophthalmic disease or a metabolic disorder using the compounds disclosed herein.

  公开号：

  WO2023137166A1
• 作为产物：
  描述：

  alkaline earth salt of/the/ methylsulfuric acid 在 盐酸 、 tin(ll) chloride 作用下， 生成 (2-bromo-4-chlorophenyl)hydrazine
  参考文献：
  名称：

  The Fischer Indole Synthesis. IV. Halogen Interchange during the Zinc Halide Induced Fischer Reactions of Acetophenone 2,6-Dihalophenylhydrazones¹

  摘要：

  DOI：

  10.1021/ja01561a043

文献信息

• [EN] PYRIDINONE AND PYRIMIDINONE DERIVATIVES AS FACTOR XIA INHIBITORS<br/>[FR] DÉRIVÉS DE PYRIDINONE ET DE PYRIMIDINONE COMME INHIBITEURS DU FACTEUR XIA
  申请人：ONO PHARMACEUTICAL CO

  公开号：WO2013093484A1

  公开（公告）日：2013-06-27

  The present invention provides compounds of the general formula (I), their salts and N- oxides, and solvates and prodrugs thereof (wherein the characters are as defined in the description). The compounds of the general formula (I) are inhibitors of Factor XIa, so that they are useful in the prevention of and/or therapy for thromboembolic diseases.

  本发明提供了一般式(I)的化合物，它们的盐和N-氧化物，以及它们的溶剂合物和前药（其中字符如描述中所定义）。一般式(I)的化合物是因子XIa的抑制剂，因此它们在预防和/或治疗血栓栓塞疾病方面是有用的。
• [EN] PIPERAZINO[1,2-A]INDOL-1-ONES AND [1,4]DIAZEPINO[1,2-A]INDOL-1-ONE<br/>[FR] PIPÉRAZINO[1,2-A]INDOL-1-ONES ET [1,4]DIAZÉPINO[1,2-A]INDOL-1-ONE
  申请人：HOFFMANN LA ROCHE

  公开号：WO2014161801A1

  公开（公告）日：2014-10-09

  The present invention relates to compounds of general formula I wherein R1 is halogen, lower alkyl, lower alkoxy, lower alkyl substituted by halogen, lower alkoxy substituted by halogen or cyano; R2 is hydrogen, CF3 or lower alkyl; R3 is hydrogen, lower alkyl, lower alkenyl, lower alkinyl, heterocycloalkyl, lower alkyl substitueted by cyano, cyano, benzyl substituted by halogen, 2-oxa-6-aza-spiro[3.3]hept-6-yl or is lower alkoxy substituted by halogen; X is -CH2- or -CH2-CH2-; or to a pharmaceutically acceptable acid addition salt, to a racemic mixture or to its corresponding enantiomer and/or optical isomers thereof. The compounds may be used for the treatment of schizophrenia, obsessive-compulsive personality disorder, major depression, bipolar disorders, anxiety disorders, normal aging, epilepsy, retinal degeneration, traumatic brain injury, spinal cord injury, post-traumatic stress disorder, panic disorder, Parkinson's disease, dementia, Alzheimer's disease, mild cognitive impairment, chemotherapy-induced cognitive dysfunction, Down syndrome, autism spectrum disorders, hearing loss, tinnitus, spinocerebellar ataxia, amyotrophic lateral sclerosis, multiple sclerosis, Huntington's disease, stroke, radiation therapy, chronic stress, abuse of neuro-active drugs, such as alcohol, opiates, methamphetamine, phencyclidine and cocaine.

  本发明涉及一般式I的化合物，其中R1是卤素、较低的烷基、较低的烷氧基、由卤素取代的较低的烷基、由卤素取代的较低的烷氧基或氰基；R2是氢、三氟甲基或较低的烷基；R3是氢、较低的烷基、较低的烯基、较低的炔基、杂环烷基、由氰基取代的较低的烷基、氰基、由卤素取代的苄基、2-氧-6-氮杂螺[3.3]庚-6-基或由卤素取代的较低的烷氧基；X是-CH2-或- - -；或是其对应的对映体和/或光学异构体的药用可接受的酸盐，或是一个外消旋混合物。这些化合物可用于治疗精神分裂症、强迫性人格障碍、重性抑郁症、躁郁症、焦虑障碍、正常衰老、癫痫、视网膜退化、创伤性脑损伤、脊髓损伤、创伤后应激障碍、恐慌障碍、帕金森病、痴呆症、阿尔茨海默病、轻度认知障碍、化疗引起的认知功能障碍、唐氏综合征、自闭症谱系障碍、听力丧失、耳鸣、脊髓小脑共济失调、肌萎缩侧索硬化、多发性硬化、亨廷顿病、中风、放射治疗、慢性压力、对神经活性药物的滥用，如酒精、阿片类药物、甲基苯丙胺、芬太尼和可卡因。
• [EN] PYRIDO[4,3-B]INDOLE AND PYRIDO[3,4-B]INDOLE DERIVATIVES AND METHODS OF USE<br/>[FR] PYRIDO[4,3-B]INDOLE ET DÉRIVÉS DE PYRIDO[3,4-B]INDOLE ET PROCÉDÉS D'UTILISATION
  申请人：MEDIVATION TECHNOLOGIES INC

  公开号：WO2011103433A1

  公开（公告）日：2011-08-25

  This disclosure is directed to pyrido[4,3-b]indole and pyrido [3,4-b] indole derivatives. Pharmaceutical compositions comprising the compounds are also provided, as are methods of using the compounds in a variety of therapeutic applications, including the treatment of a cognitive disorder, psychotic disorder, neurotransmitter-mediated disorder and/or a neuronal disorder.

  本公开涉及吡啶并[4,3-b]吲哚和吡啶[3,4-b]吲哚衍生物。还提供了包含这些化合物的药物组合物，以及使用这些化合物在各种治疗应用中的方法，包括治疗认知障碍、精神障碍、神经递质介导的障碍和/或神经元障碍。
• [EN] INDOL-CARBOXAMIDE DERIVATIVES<br/>[FR] DÉRIVÉS D'INDOLE-CARBOXAMIDE
  申请人：HOFFMANN LA ROCHE

  公开号：WO2015036412A1

  公开（公告）日：2015-03-19

  The present invention relates to compounds of general formula (I) wherein R1 is aryl or heteroaryl, which are optionally substituted by one, two or three substituents, selected from lower alkyl, halogen, lower alkyl substituted by halogen, hydroxy, lower alkyl substituted by hydroxy, lower alkoxy, lower alkoxy substituted by halogen, cyano or nitro; R 2 is halogen, lower alkyl or cyano; R 3 is hydrogen, lower alkyl or lower alkyl substituted by halogen; R 4 is hydrogen or lower alkyl; R5, R 6 are hydrogen, lower alkyl, or may form together with the N-atom to which they are attached a heterocycloalkyl ring; or a pharmaceutically acceptable acid addition salt, a racemic mixture or its corresponding enantiomer and/or optical isomers thereof. The compounds may be used for the treatment of schizophrenia, obsessive-compulsive personality disorder, major depression, bipolar disorders, anxiety disorders, normal aging, epilepsy, retinal degeneration, traumatic brain injury, spinal cord injury, post-traumatic stress disorder, panic disorder, Parkinson's disease, dementia, Alzheimer's disease, cognitive impairment, chemotherapy-induced cognitive dysfunction ("chemobrain"), Down syndrome, autism spectrum disorders, hearing loss, tinnitus, spinocerebellar ataxia, amyotrophic lateral sclerosis, multiple sclerosis, Huntington's disease, stroke, and disturbances due to radiation therapy, chronic stress, or abuse of neuro-active drugs, selected from alcohol, opiates, methamphetamine, phencyclidine and cocaine.

  本发明涉及通式（I）的化合物，其中R1是芳基或杂环芳基，可以选择地被一个、两个或三个取代基取代，所选取代基包括较低的烷基、卤素、被卤素取代的较低的烷基、羟基、被羟基取代的较低的烷基、烷氧基、被卤素取代的烷氧基、氰基或硝基；R2是卤素、较低的烷基或氰基；R3是氢、较低的烷基或被卤素取代的较低的烷基；R4是氢或较低的烷基；R5、R6是氢、较低的烷基，或者可以与它们附着的N原子一起形成一个杂环烷基环；或者是药学上可接受的酸盐加合物，外消旋混合物或其对应的对映体和/或光学异构体。这些化合物可用于治疗精神分裂症、强迫性人格障碍、重度抑郁症、躁郁症、焦虑障碍、正常衰老、癫痫、视网膜退行性疾病、创伤性脑损伤、脊髓损伤、创伤后应激障碍、恐慌障碍、帕金森病、痴呆症、阿尔茨海默病、认知障碍、化疗诱导的认知功能障碍（"化疗脑"）、唐氏综合征、自闭症谱系障碍、听力丧失、耳鸣、脊髓小脑共济失调、肌萎缩性侧索硬化、多发性硬化症、亨廷顿病、中风，以及由放疗、慢性压力或神经活性药物（包括酒精、鸦片、甲基苯丙胺、芬太尼和可卡因）滥用引起的干扰。
• COMPOUNDS AND METHODS OF TREATING HYPERTENSION
  申请人：Protter Andrew Asher

  公开号：US20140303144A1

  公开（公告）日：2014-10-09

  Hydrogenated pyrido[4,3-b]indoles, pyrido[3,4-b]indoles and azepino[4,5-b]indoles are described. The compounds may bind to and are adrenergic receptor α 2B antagonists. The compounds may also bind to and antagonize adrenergic receptor α 2B . The compounds may find use in therapy, e.g., to (i) reduce blood pressure and/or (ii) promote renal blood flow and/or (iii) decrease or inhibit sodium reabsorption. The compounds may also be used to treat diseases or conditions that are, or are expected to be, responsive to a decrease in blood pressure. Use of the compounds to treat cardiovascular and renal disorders is particularly described.

  本文介绍了氢化吡啶[4,3-b]吲哚、吡啶[3,4-b]吲哚和氮杂七环[4,5-b]吲哚。这些化合物可以与肾上腺素受体α2B结合并对其产生拮抗作用。这些化合物还可以与肾上腺素受体α2B结合并对其产生拮抗作用。这些化合物可以用于治疗，例如：（i）降低血压和/或（ii）促进肾脏血流和/或（iii）减少或抑制钠的重吸收。这些化合物还可以用于治疗对降低血压有反应或预计会有反应的疾病或病况。特别描述了这些化合物用于治疗心血管和肾脏疾病。