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5-溴-3-甲基-1-苯并噻吩-2-磺酰氯 | 338797-11-8

中文名称
5-溴-3-甲基-1-苯并噻吩-2-磺酰氯
中文别名
——
英文名称
5-bromo-3-methyl-benzo[b]thiophene-2-sulfonyl chloride
英文别名
5-bromo-3-methylbenzothiophene-2-sulfonyl chloride;5-Bromo-3-methylbenzo[b]thiophene-2-sulphonyl chloride;5-bromo-3-methyl-1-benzothiophene-2-sulfonyl chloride
5-溴-3-甲基-1-苯并噻吩-2-磺酰氯化学式
CAS
338797-11-8
化学式
C9H6BrClO2S2
mdl
——
分子量
325.634
InChiKey
YSXQHKIUGBLJKG-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:
    433.1±45.0 °C(Predicted)
  • 密度:
    1.787±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    4.4
  • 重原子数:
    15
  • 可旋转键数:
    1
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.11
  • 拓扑面积:
    70.8
  • 氢给体数:
    0
  • 氢受体数:
    3

安全信息

  • 海关编码:
    2934999090

SDS

SDS:0142701c139e85bde0c7c811b8986843
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上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量
  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

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文献信息

  • NEW AMINOTHIAZOLES AS FBPASE INHIBITORS FOR DIABETES
    申请人:Hebeisen Paul
    公开号:US20090143448A1
    公开(公告)日:2009-06-04
    Compounds of formula (I) as well as pharmaceutically acceptable salts and esters thereof, wherein R 1 to R 3 have the significance given in claim 1 and which can be used in the form of pharmaceutical compositions.
    式(I)的化合物以及其药用可接受的盐和酯,其中R1至R3具有权利要求1中给定的含义,并可用于制成药物组合物。
  • Amino heterocyclyl inhibitors of 11-beta-hydroxy steroid dehydrogenase type 1
    申请人:Cheng Hengmiao
    公开号:US20050148631A1
    公开(公告)日:2005-07-07
    The present invention relates to compounds with the formula (I), or a pharmaceutically acceptable salt thereof: The invention also relates to pharmaceutical compositions comprising the compounds of formula (I) or formula (II) and methods of treating a condition that is mediated by the modulation of 11-β-hsd-1, the method comprising administering to a mammal an effective amount of a compound of formula (I) or formula (II).
    本发明涉及具有化学式(I)或其药学上可接受的盐的化合物:该发明还涉及包含化学式(I)或化学式(II)化合物的药物组合物,以及治疗通过调节11-β-hsd-1介导的疾病的方法,该方法包括向哺乳动物施用化学式(I)或化学式(II)化合物的有效量。
  • [EN] BIS-SULFONAMIDE DERIVATIVES, COMPOSITIONS, AND METHODS OF USE<br/>[FR] DÉRIVÉS DE BIS-SULFONAMIDE, COMPOSITIONS ET PROCÉDÉS D'UTILISATION
    申请人:HIGH POINT PHARMACEUTICALS LLC
    公开号:WO2011022207A1
    公开(公告)日:2011-02-24
    Embodiments of the present invention provide bissulfonamide derivtives and pharmaceutical compositions comprising bissulfonamide derivatives. Methods of use of such compounds and compositions to reduce neuropathic pain in a subject are also provided.
    本发明实施例提供双磺酰胺衍生物和包括双磺酰胺衍生物的药物组合物。还提供了使用这些化合物和组合物来减少受试者神经病理性疼痛的方法。
  • N-SULFONYL THIAZOLYLPIPERAZINE DERIVATIVES AND RELATED N-SULFONYL HETEROCYCLIC DERIVATIVES FOR THE TREATMENT OF NEURO DEGENERATIVE DISEASES
    申请人:GRIFFIOEN Gerard
    公开号:US20100197703A1
    公开(公告)日:2010-08-05
    This invention provides thiazolylpiperazine derivatives, and N-sulfonyl heterocyclic derivatives including phenyl- and benzyl-thiazolylpiperidine derivatives, and pharmaceutically acceptable salts thereof, which are useful active ingredients for administration in a method for the treatment of an α-synucleopathy such as Parkinson's disease, diffuse Lewy body disease, traumatic brain injury, amyotrophic lateral sclerosis, Niemann-Pick disease, Hallervorden-Spatz syndrome, Down syndrome, neuroaxonal dystrophy, multiple system atrophy and Alzheimer's disease. This invention also provides methods for making such derivatives, and pharmaceutical compositions including such derivatives together with pharmaceutically acceptable excipients.
    该发明提供了噻唑基哌嗪衍生物,以及包括苯基和苄基噻唑基哌啶衍生物的N-磺酰杂环衍生物,以及其药学上可接受的盐,这些是用于治疗α-突触核蛋白病的有效活性成分,如帕金森病、弥漫性小体病、创伤性脑损伤、肌萎缩侧索硬化症、尼曼-匹克病、哈勒沃登-施帕茨综合征、唐氏综合征、神经轴突萎缩、多系统萎缩和阿尔茨海默病的治疗方法。该发明还提供了制备这些衍生物的方法,以及包括这些衍生物和药学上可接受的辅料的药物组合物。
  • [EN] BENZENESULFONYLAMINO-PYRIDIN-2-YL DERIVATIVES AND RELATED COMPOUNDS AS INHIBITORS OF 11-BETA-HYDROXY STEROID DEHYDROGENASE TYPE 1 (11-BETA-HSD-1) FOR THE TREATMENT OF DIABETES AND OBESITY<br/>[FR] DERIVES DE BENZENESULFONYLAMINO-PYRIDIN-2-YL ET COMPOSES APPARENTES EN TANT QU'INHIBITEURS DE LA 11-BETA-HYDROXYSTEROIDE DESHYDROGENASE TYPE 1 (11-BETA-HSD-1) POUR LE TRAITEMENT DU DIABETE ET DE L'OBESITE
    申请人:PFIZER
    公开号:WO2005060963A1
    公开(公告)日:2005-07-07
    The present invention relates to compounds with the formula (I), or a pharmaceutically acceptable satt thereof, formula (I), wherein: R' is selected from the group consisting of (C1--C6)alkyl, -(CR<3>R<4>),(C3-C12)cycloalkyl, -(CR<3>R<4>),(C6-C12)aryl, and -(CR<3>R<4>)t(410)-membered heterocyclyl; b and k are each independently selected from 1 and 2; j is selected from the group consisting of 0, 1, and 2; t, u, p, q, and v are each independently selected from the group consisting of 0, 1, 2, 3, 4, and 5; T is a (6-10)-membered heterocyclyl containing at least one nitrogen atom; R<2> is selected from the group consisting of H, (C1-C6)alkyl, -(CR<3>R)t(C3-C12)cycloalkyl, -(CR<3>R<4>)t(C6-C12)aryt, and -(CR<3>R<4>)t(410)-membered heterocyclyl; each R<3 >and R<4>.is independently selected from H and (C1-C6)alkyl, the carbon atoms of T, R', R<2>,< >R<3> and R<4> may each be optionally, substituted by I to 5 R<5> groups; Ris defined in the claims; The compounds of the present invention are 11 ß-hsd-1 inhibitors, and are therefore believed to be useful in the treatment of diabetes, obesity, glaucoma, osteoporosis, cognitive disorders, immune disorders, depression, hypertension, and metabolic diseases.
    本发明涉及具有公式(I)的化合物或其药学上可接受的盐,公式(I)中:R'从(C1-C6)烷基,-(CR<3>R<4>),(C3-C12)环烷基,-(CR<3>R<4>),(C6-C12)芳基和-(CR<3>R<4>)t(4-10)成员杂环基组成的群体中选择;b和k各自独立地选择为1和2;j从0、1和2的群体中选择;t、u、p、q和v各自独立地从0、1、2、3、4和5的群体中选择;T是一个至少含有一个氮原子的(6-10)成员杂环基;R<2>从H、(C1-C6)烷基,-(CR<3>R)t(C3-C12)环烷基,-(CR<3>R<4>)t(C6-C12)芳基和-(CR<3>R<4>)t(4-10)成员杂环基中选择;每个R<3>和R<4>独立地从H和(C1-C6)烷基中选择,T、R'、R<2>、R<3>和R<4>的碳原子可以选择地被1-5个R<5>基团取代;R在权利要求中定义;本发明的化合物是11ß-hsd-1抑制剂,因此被认为在糖尿病、肥胖症、青光眼、骨质疏松症、认知障碍、免疫障碍、抑郁症、高血压和代谢性疾病的治疗中有用。
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