(4-bromophenyl)(3-pyridyl)methanol | 63779-12-4

• 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-bromophenyl)(3-pyridyl)methanol
• 英文别名: (4-bromophenyl)(pyridin-3-yl)methanol；(4-bromophenyl)-pyridin-3-ylmethanol
• CAS: 63779-12-4
• 化学式: C₁₂H₁₀BrNO
• 分子量: 264.121
• InChiKey: QPNDEHPTNNQRTR-UHFFFAOYSA-N

物化性质

• 熔点：
  125-126 °C
• 沸点：
  419.2±35.0 °C(Predicted)
• 密度：
  1.496±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  2.4
• 重原子数：
  15
• 可旋转键数：
  2
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.08
• 拓扑面积：
  33.1
• 氢给体数：
  1
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  (4-bromophenyl)(3-pyridyl)methanol 、 碘甲烷 以 N,N-二甲基甲酰胺 为溶剂， 反应 2.0h， 以55%的产率得到3-((4-bromophenyl)(methoxy)methyl)pyridine
  参考文献：
  名称：

  EP2166015

  摘要：

  公开号：
• 作为产物：
  描述：

  3-溴吡啶 、 对溴苯甲醛 在 crude residue 、 silica gel 、 甲醇 、 二氯甲烷 作用下， 生成 (4-bromophenyl)(3-pyridyl)methanol
  参考文献：
  名称：

  Cathepsin cysteine protease inhibitors

  摘要：

  本发明涉及一类化合物，它们是半胱氨酸蛋白酶抑制剂，包括但不限于对卡特普辛K、L、S和B的抑制剂。这些化合物可用于治疗需要抑制骨吸收的疾病，如骨质疏松症。它们具有以下结构式：式（I）。

  公开号：

  US07279478B2

文献信息

• [EN] CATHEPSIN CYSTEINE PROTEASE INHIBITORS<br/>[FR] INHIBITEURS DE PROTEASES A CYSTEINE DE TYPE CATHEPSINE
  申请人：MERCK FROSST CANADA INC

  公开号：WO2004022526A1

  公开（公告）日：2004-03-18

  This invention relates to class of compounds which are cysteine protease inhibitors, including but not limited to, inhibitors of cathepsins K, L, S and B. These compounds are useful for treating diseases in which inhibition of bone resorption is indicated, such as osteoporosis. They have the following structure: Formula (I).

  这项发明涉及一类化合物，这些化合物是半胱氨酸蛋白酶抑制剂，包括但不限于对卡特普辛K、L、S和B的抑制剂。这些化合物可用于治疗需要抑制骨吸收的疾病，如骨质疏松症。它们具有以下结构：化学式（I）。
• LINCOSAMIDE DERIVATIVES AND ANTIMICROBIAL AGENTS COMPRISING THE SAME AS ACTIVE INGREDIENT
  申请人：Umemura Eijirou

  公开号：US20100184746A1

  公开（公告）日：2010-07-22

  An objective of the present invention is to provide compounds of formula (I) or their pharmacologically acceptable salts or solvates wherein A represents aryl while R 1 represents a five- or six-membered monocyclic heterocyclic group, or A represents a four- to six-membered monocyclic heterocyclic group while R 1 represents aryl or a five- or six-membered monocyclic heterocyclic group; R 2 represents a hydrogen atom or C 1-6 alkyl; R 3 represents C 1-6 alkyl or C 3-6 cycloalkyl-C 1-4 alkyl; R 4 , R 5 , and R 6 represent a hydrogen atom; R 7 represents C 1-6 alkyl; and m is 1 to 3. The compounds are novel lincosamide derivatives that have a potent activity against resistant Streptococcus pneumoniae . Further, the compounds are usable as antimicrobial agents and are useful for preventing or treating bacterial infectious diseases.

  本发明的目标是提供式（I）的化合物或其药理学上可接受的盐或溶剂，其中A代表芳基，而R1代表五元或六元单环杂环基，或A代表四至六元单环杂环基，而R1代表芳基或五元或六元单环杂环基；R2代表氢原子或C1-6烷基；R3代表C1-6烷基或C3-6环烷基-C1-4烷基；R4、R5和R6代表氢原子；R7代表C1-6烷基；m为1至3。这些化合物是新型的林可霉素衍生物，对耐药性肺炎链球菌具有强效活性。此外，这些化合物可用作抗微生物剂，对预防或治疗细菌感染性疾病有用。
• Lincosamide derivatives and antimicrobial agents comprising the same as active ingredient
  申请人：Meiji Seika Kaisha, Ltd.

  公开号：US07867980B2

  公开（公告）日：2011-01-11

  An objective of the present invention is to provide compounds of formula (I) or their pharmacologically acceptable salts or solvates wherein A represents aryl while R1 represents a five- or six-membered monocyclic heterocyclic group, or A represents a four- to six-membered monocyclic heterocyclic group while R1 represents aryl or a five- or six-membered monocyclic heterocyclic group; R2 represents a hydrogen atom or C1-6 alkyl; R3 represents C1-6 alkyl or C3-6 cycloalkyl-C1-4 alkyl; R4, R5, and R6 represent a hydrogen atom; R7 represents C1-6 alkyl; and m is 1 to 3. The compounds are novel lincosamide derivatives that have a potent activity against resistant Streptococcus pneumoniae. Further, the compounds are usable as antimicrobial agents and are useful for preventing or treating bacterial infectious diseases.

  本发明的目标是提供式（I）的化合物或其药学上可接受的盐或溶剂，其中A代表芳基，而R1代表五元或六元单环杂环基，或A代表四元至六元单环杂环基，而R1代表芳基或五元或六元单环杂环基；R2代表氢原子或C1-6烷基；R3代表C1-6烷基或C3-6环烷基-C1-4烷基；R4、R5和R6代表氢原子；R7代表C1-6烷基；m为1至3。这些化合物是新型的林可霉素衍生物，对耐药性肺炎链球菌有强效活性。此外，这些化合物可用作抗微生物剂，并可用于预防或治疗细菌感染性疾病。
• LINCOSAMIDE DERIVATIVE, AND ANTIBACTERIAL AGENT COMPRISING THE SAME AS ACTIVE INGREDIENT
  申请人：Meiji Seika Kaisha Ltd.

  公开号：EP2166015A1

  公开（公告）日：2010-03-24

  An objective of the present invention is to provide compounds of formula (I) or their pharmacologically acceptable salts or solvates wherein A represents aryl while R1 represents a five- or six-membered monocyclic heterocyclic group, or A represents a four- to six-membered monocyclic heterocyclic group while R1 represents aryl or a five- or six-membered monocyclic heterocyclic group; R2 represents a hydrogen atom or C1-6 alkyl; R3 represents C1-6 alkyl or C3-6 cycloalkyl-C1-4 alkyl; R4, R5, and R6 represent a hydrogen atom; R7 represents C1-6 alkyl; and m is 1 to 3. The compounds are novel lincosamide derivatives that have a potent activity against resistant Streptococcus pneumoniae. Further, the compounds are usable as antimicrobial agents and are useful for preventing or treating bacterial infectious diseases.

  本发明的目的是提供式(I)化合物或其药理学上可接受的盐或溶液，其中 A 代表芳基，而 R1 代表五元或六元单环杂环基团，或 A 代表四至六元单环杂环基团，而 R1 代表芳基或五元或六元单环杂环基团；R2代表氢原子或C1-6烷基；R3代表C1-6烷基或C3-6环烷基-C1-4烷基；R4、R5和R6代表氢原子；R7代表C1-6烷基；m为1至3。这些化合物是新型林可酰胺衍生物，对耐药性肺炎链球菌具有强效活性。此外，这些化合物还可用作抗菌剂，用于预防或治疗细菌感染性疾病。
• CATHEPSIN CYSTEINE PROTEASE INHIBITORS
  申请人：MERCK FROSST CANADA INC.

  公开号：EP1537074A1

  公开（公告）日：2005-06-08