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1-(m-Chlorphenyl)-3-methyl-3-azabicyclo<3.1.0>hexan | 86215-54-5

中文名称
——
中文别名
——
英文名称
1-(m-Chlorphenyl)-3-methyl-3-azabicyclo<3.1.0>hexan
英文别名
1-(3-chlorophenyl)-3-methyl-3-aza-bicyclo[3.1.0]hexane;1-(3-Chlorophenyl)-3-methyl-3-azabicyclo[3.1.0]hexane
1-(m-Chlorphenyl)-3-methyl-3-azabicyclo<3.1.0>hexan化学式
CAS
86215-54-5
化学式
C12H14ClN
mdl
——
分子量
207.703
InChiKey
OKEDSONVVYDIAB-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

物化性质

  • 沸点:
    286.0±23.0 °C(Predicted)
  • 密度:
    1.225±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.54
  • 重原子数:
    14.0
  • 可旋转键数:
    1.0
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.5
  • 拓扑面积:
    3.24
  • 氢给体数:
    0.0
  • 氢受体数:
    1.0

文献信息

  • [EN] 2,3-DIHYDRO-6-NITROIMIDAZO (2,1-B) OXAZOLE COMPOUNDS FOR THE TREATMENT OF TUBERCULOSIS<br/>[FR] COMPOSES 2,3-DIHYDRO-6-NITROIMIDAZO (2,1-B) OXAZOLE POUR LE TRAITEMENT DE LA TUBERCULOSE
    申请人:OTSUKA PHARMA CO LTD
    公开号:WO2005042542A1
    公开(公告)日:2005-05-12
    The present invention provides a 2,3-dihydro-6-nitroimidazo[2,1-b]oxazole compound represented by the following general formula: (1)in the above formula (1), R1 represents a hydrogen atom or C1-C6 alkyl group, n represents an integer of 0 to 6, R1 and -(CH2)nR2 may form a spiro ring represented by the formula (30) below, together with the adjacent carbon atom (in the formula below, RRR represents a piperidyl group which may have substituents on the piperidine ring), (30)and R2 represents a benzothiazolyloxy group, quinolyloxy group, pyridyloxy group or the like. The present compound has an excellent bactericidal action against Mycobacterium tuberculosis, multi-drug-resistant Mycobacterium tuberculosis, and atypical acid-fast bacteria.
    本发明提供了一种由以下一般式表示的2,3-二氢-6-硝基咪唑[2,1-b]噁唑化合物:(1)在上述式(1)中,R1代表氢原子或C1-C6烷基,n代表0至6的整数,R1和-(CH2)nR2可以与下面的式(30)一起形成一个螺环,与相邻的碳原子一起(在下面的式中,RRR代表可能在哌啶环上具有取代基的哌啶基),(30)和R2代表苯并噻唑氧基、喹啉氧基、吡啶氧基或类似物。该化合物对结核分枝杆菌、多药耐药结核分枝杆菌和非典型耐酸细菌具有出色的杀菌作用。
  • Methods and compositions for production, formulation and use of 1-aryl-3-azabicyclo[3.1.0]hexanes
    申请人:Skolnick Phil
    公开号:US20060223875A1
    公开(公告)日:2006-10-05
    The invention provides novel 1-aryl-3-azabicyclo[3.1.0]hexanes that are active for modulating biogenic amine transport, along with compositions and methods for using these compounds to treat central nervous system disorders. Certain 1-aryl-3-azabicyclo[3.1.0]hexanes are provided that have at least one substituent on the aryl ring. In other embodiments 1-aryl-3-azabicyclo[3.1.0]hexanes are provided that have a substitution on the nitrogen at the ‘3’ position. In additional embodiments 1-aryl-3-azabicyclo[3.1.0]hexanes are provided which have one substitution on the aryl ring, as well as a substitution on the nitrogen at the ‘3’ position. The invention also provides novel methods of making aryl- and aza-substituted 1-aryl-3-azabicyclo[3.1.0]hexanes, including synthetic methods that form novel intermediate compounds of the invention for producing aryl- and aza-substituted 1-aryl-3-azabicyclo[3.1.0]hexanes.
    本发明提供了新型的1-芳基-3-氮杂双环[3.1.0]己烷,它们对生物胺转运的调节具有活性,以及使用这些化合物治疗中枢神经系统疾病的组合物和方法。提供了某些1-芳基-3-氮杂双环[3.1.0]己烷,其在芳基环上至少有一个取代基。在其他实施例中,提供了在“3”位的氮上有取代基的1-芳基-3-氮杂双环[3.1.0]己烷。在其他实施例中,提供了在芳基环上有一个取代基以及在“3”位的氮上有一个取代基的1-芳基-3-氮杂双环[3.1.0]己烷。本发明还提供了制备芳基和氮取代的1-芳基-3-氮杂双环[3.1.0]己烷的新方法,包括形成本发明的新中间化合物的合成方法,用于生产芳基和氮取代的1-芳基-3-氮杂双环[3.1.0]己烷
  • Methods and compositions for the treatment of neuropathies and related disorders
    申请人:Lippa S. Arnold
    公开号:US20070082939A1
    公开(公告)日:2007-04-12
    The present invention provides novel compositions and methods for treating symptoms associated with neuropathic disorders such as hyperalgesia, allodynia, and parasthesias, using a 1-aryl-3-azabicyclo[3.1.0] hexane. The invention further relates to the use of 1-aryl-3-azabicyclo[3.1.0] hexanes in pharmaceutical compositions and methods for treating neuropathic disorders and related symptoms in mammals. Patients amenable to treatment according to the invention include those suffering from diabetic neuropathies, post-herpetic neuralgia, trigeminal neuralgia, chronic lower back pain, sciatica, idiopathic and post-traumatic neuropathies, HIV-associated neuropathic pain, among many other neuropathic disorders and related symptoms.
    本发明提供了一种新型组合物和方法,用于治疗与神经病理性疾病相关的症状,如过度疼痛、触痛和感觉异常,使用1-芳基-3-氮杂双环[3.1.0]己烷。本发明还涉及在制药组合物中使用1-芳基-3-氮杂双环[3.1.0]己烷以及治疗哺乳动物神经病理性疾病和相关症状的方法。根据本发明可治疗的患者包括患有糖尿病神经病变、带状疱疹后遗神经痛、三叉神经痛、慢性腰痛、坐骨神经痛、特发性和创伤后神经病变、HIV相关神经病理性疼痛等许多神经病理性疾病和相关症状的患者。
  • 2,3-DIHYDRO-6-NITROIMIDAZO [2,1-B] OXAZOLE COMPOUNDS FOR THE TREATMENT OF TUBERCULOSIS
    申请人:OTSUKA PHARMACEUTICAL CO., LTD.
    公开号:EP1678185A1
    公开(公告)日:2006-07-12
  • [EN] METHODS AND COMPOSITIONS FOR THE TREATMENT OF NEUROPATHIES AND RELATED DISORDERS<br/>[FR] PROCEDES ET COMPOSITIONS POUR LE TRAITEMENT DE NEUROPATHIES ET DE TROUBLES CONNEXES
    申请人:DOV PHARMACEUTICAL INC
    公开号:WO2007014264A2
    公开(公告)日:2007-02-01
    [EN] The present invention provides novel compositions and methods for treating symptoms associated with neuropathic disorders such as hyperalgesia, allodynia, and parasthesias, using a l-aryl-3-azabicyclo[3.1.0] hexane. The invention further relates to the use of l-aryl-3-azabicyclo[3.1.0] hexanes in pharmaceutical compositions and methods for treating neuropathic disorders and related symptoms in mammals. Patients amenable to treatment according to the invention include those suffering from diabetic neuropathies, post-herpetic neuralgia, trigeminal neuralgia, chronic lower back pain, sciatica, idiopathic and post-traumatic neuropathies, HIV-associated neuropathic pain, among many other neuropathic disorders and related symptoms.
    [FR] L'invention concerne de nouvelles compositions ainsi que des procédés permettant de traiter des symptômes associés à des troubles neuropathiques, par exemple hyperalgie, allodynie, et parasthésie, à l'aide de 1-aryl-3-azabicyclo[3.1.0] hexane. L'invention concerne également l'utilisation de 1-aryl-3-azabicyclo[3.1.0] hexanes dans des compositions pharmaceutiques et des procédés de traitement de troubles neuropathiques et de symptômes connexes chez les mammifères. Les patients pouvant faire l'objet de ce traitement selon l'invention sont notamment ceux qui souffrent de neuropathies diabétiques, de névralgie post-herpétique, de névralgie faciale, de douleurs lombaires, de sciatique, de neuropathies idiopathiques et post-traumatiques, de douleurs neuropathiques associées au VIH, entre bon nombre d'autres troubles neuropathiques et symptômes connexes.
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