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2-bromo-4-methylsulfanyl-pyridine | 1193244-91-5

中文名称
——
中文别名
——
英文名称
2-bromo-4-methylsulfanyl-pyridine
英文别名
2-Bromo-4-(methylthio)pyridine;2-bromo-4-methylsulfanylpyridine
2-bromo-4-methylsulfanyl-pyridine化学式
CAS
1193244-91-5
化学式
C6H6BrNS
mdl
——
分子量
204.09
InChiKey
BCTAQQXOKMHCFD-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

计算性质

  • 辛醇/水分配系数(LogP):
    2.4
  • 重原子数:
    9
  • 可旋转键数:
    1
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.17
  • 拓扑面积:
    38.2
  • 氢给体数:
    0
  • 氢受体数:
    2

反应信息

  • 作为反应物:
    描述:
    2-氟-4-碘吡啶2-bromo-4-methylsulfanyl-pyridine 生成 4-iodo-2-(methylthio)pyridine
    参考文献:
    名称:
    Cyclic Inhibitors Of 11Beta-Hydroxysteroid Dehydrogenase 1
    摘要:
    本发明涉及一种新型化合物I、Ik、Iq1-21、Ir1-21、Is1-21、It1-7,其药学上可接受的盐以及其制备的药物组合物。该化合物可用于治疗与哺乳动物中11β-HSD1的调节或抑制有关的疾病。本发明还涉及该新型化合物的药物组合物以及它们在细胞中降低或控制皮质醇的产生或抑制皮质酮转化为皮质醇的方法。
    公开号:
    US20110263584A1
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文献信息

  • [EN] NOVEL SUBSTITUTED PYRIMIDINE COMPOUNDS<br/>[FR] NOUVEAUX COMPOSÉS DE PYRIMIDINE SUBSTITUÉS
    申请人:GRUENENTHAL GMBH
    公开号:WO2016008593A1
    公开(公告)日:2016-01-21
    The invention relates to novel substituted pyrimidine compounds of general formula (I), in which the chemical groupings, substituents, variables and indices are as defined in the description, and to their use as medicaments, in particular as medicaments for the treatment of conditions and diseases that can be treated by inhibition of the PDE4 enzyme.
    该发明涉及一种新型取代嘧啶化合物,其一般式为(I),其中化学基团、取代基、变量和指数如描述中所定义,并且其用作药物,特别是用作治疗可以通过抑制PDE4酶来治疗的疾病和病症的药物。
  • Triphenylphosphine derivative, production process therefor, palladium complex thereof, and process for producing biaryl derivative
    申请人:——
    公开号:US20030065208A1
    公开(公告)日:2003-04-03
    Provided are a novel triphenyl phosphine derivative synthesized from a triphenylphosphine and a hydroxy-containing lactone; a palladium and a nickel complexes comprising the derivative as a ligand; and a process for preparing a biaryl derivative using the complex as a catalyst. A product can be easily separated from a catalyst or a phosphorus compound, and biaryl derivative can be synthesized in a higher yield, by using the complex of the present invention as a catalyst.
    提供了一种新型的三苯基膦衍生物,通过三苯基膦和含羟基的内酯合成;一种以该衍生物为配体的钯和镍配合物;以及一种利用该配合物作为催化剂制备联苯衍生物的方法。通过使用本发明的复合物作为催化剂,产品可以很容易地与催化剂或磷化合物分离,联苯衍生物可以以更高的产率合成。
  • Cyclic Inhibitors Of 11Beta-Hydroxysteroid Dehydrogenase 1
    申请人:Claremon David A.
    公开号:US20110263584A1
    公开(公告)日:2011-10-27
    This invention relates to novel compounds of the Formula I, Ik, Iq 1-21 , Ir 1-21 , Is 1-21 , It 1-7 , pharmaceutically acceptable salts thereof, and pharmaceutical compositions thereof, which are useful for the therapeutic treatment of diseases associated with the modulation or inhibition of 11 β-HSD1 in mammals. The invention further relates to pharmaceutical compositions of the novel compounds and methods for their use in the reduction or control of the production of cortisol in a cell or the inhibition of the conversion of cortisone to cortisol in a cell.
    本发明涉及一种新型化合物I、Ik、Iq1-21、Ir1-21、Is1-21、It1-7,其药学上可接受的盐以及其制备的药物组合物。该化合物可用于治疗与哺乳动物中11β-HSD1的调节或抑制有关的疾病。本发明还涉及该新型化合物的药物组合物以及它们在细胞中降低或控制皮质醇的产生或抑制皮质酮转化为皮质醇的方法。
  • Novel substituted pyrimidine compounds
    申请人:Grünenthal GmbH
    公开号:US20160016937A1
    公开(公告)日:2016-01-21
    The invention relates to novel substituted pyrimidine compounds of general formula (I) in which the chemical groupings, substituents, variables and indices are as defined in the description, and to their use as medicaments, in particular as medicaments for the treatment of conditions and diseases that can be treated by inhibition of the PDE4 enzyme.
    本发明涉及一种新颖的取代嘧啶化合物,其一般式为(I),其中化学基团,取代基,变量和指数如描述中所定义,并且它们作为药物的使用,特别是作为治疗可以通过抑制PDE4酶治疗的疾病和病症的药物。
  • TRIPHENYLPHOSPHINE DERIVATIVE, PRODUCTION PROCESS THEREFOR, PALLADIUM COMPLEX THEREOF, AND PROCESS FOR PRODUCING BIARYL DERIVATIVE
    申请人:Mitsubishi Rayon Co., Ltd.
    公开号:EP1270582A1
    公开(公告)日:2003-01-02
    Provided are a novel triphenyl phosphine derivative synthesized from a triphenylphosphine and a hydroxy-containing lactone; a palladium and a nickel complexes comprising the derivative as a ligand; and a process for preparing a biaryl derivative using the complex as a catalyst. A product can be easily separated from a catalyst or a phosphorus compound, and biaryl derivative can be synthesized in a higher yield, by using the complex of the present invention as a catalyst.
    本发明提供了一种由三苯基膦和含羟基内酯合成的新型三苯基膦衍生物;一种以该衍生物为配体的钯和镍配合物;以及一种以该配合物为催化剂制备双芳基衍生物的工艺。使用本发明的配合物作为催化剂,产物可以很容易地从催化剂或磷化合物中分离出来,并且可以以更高的产率合成双芳基衍生物。
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