2-(benzylsulfanyl)-6-bromo-1H-imidazo[4,5-b]pyridine

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 咪唑并吡啶类
• 英文名称: 2-(benzylsulfanyl)-6-bromo-1H-imidazo[4,5-b]pyridine
• 英文别名: 2-benzylsulfanyl-6-bromo-1H-imidazo[4,5-b]pyridine
• 化学式: C₁₃H₁₀BrN₃S
• 分子量: 320.21
• InChiKey: MOECSMFBXSQKSZ-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.8
• 重原子数：
  18
• 可旋转键数：
  3
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.08
• 拓扑面积：
  66.9
• 氢给体数：
  1
• 氢受体数：
  3

文献信息

• Pharmaceutical compositions and methods for use
  申请人：——

  公开号：US20020058652A1

  公开（公告）日：2002-05-16

  The present invention relates to aryl olefinic azacyclic compounds and aryl acetylenic azacyclic compounds, including pyridyl olefinic cycloalkylamines and pyridyl acetylenic cycloalkylamines. The present invention also relates to prodrug derivatives of the compounds of the present invention.

  本发明涉及芳基烯丙基氮杂环化合物和芳基炔丙基氮杂环化合物，包括吡啶基烯丙基环烷基胺和吡啶基炔丙基环烷基胺。本发明还涉及本发明化合物的药物前体衍生物。
• [EN] PHARMACEUTICAL COMPOSITIONS AND METHODS FOR USE<br/>[FR] COMPOSITIONS PHARMACEUTIQUES ET METHODES D'UTILISATION
  申请人：TARGACEPT INC

  公开号：WO2000075110A1

  公开（公告）日：2000-12-14

  Pharmaceutical compositions incorporate aryl substituted olefinic amine compounds. Representative compounds are (2S)-(4E)-N-methyl-5-[3-(5-isopropoxy-1-oxopyridin)yl)]-4-penten-2-amine, (3E)-N-methyl-4-(3-(1-oxopyridin)yl)-3-buten-1-amine, (4E)-N-methyl-5-(3-(1-oxopyridin)yl)-4-penten-2-amine, (4E)-N-methyl-5-(3-(5-((carboxymethyl)oxy)pyridin)yl)-4-penten-2-amine, (3E)-N-methyl-4-[3-(5-nitro-6-aminopyridin)yl]-3-buten-1-amine, (3E)-N-methyl-4-[3-(5-(N-benzylcarboxamido)pyridin)yl]-3-buten-1-amine(4E)-N-methyl-5-[5-(2-aminopyrimidin)yl]-4-penten-2-amine, (4E)-N-methyl-5-(3-(5-aminopyridin)yl)-4-penten-2-amine (3E)-N-methyl-4-(3-(5-isobutoxypyridin)yl)-3-buten-1-amine, (3E)-N-methyl-4-(3-(5-ethylthiopyridin)yl)-3-buten-1-amine, (4E)-N-methyl-5-(3-(5-trifluoromethylpyridin)yl)-4-penten-2-amine, (4E)-5-(3-(5-isopropoxypyridin)yl)-4-penten-2-amine, and (4E)-5-(3-(5-isopropoxypyridin)yl)-4-penten-2-amine.

  制药组合物包括芳基取代烯丙胺化合物。代表性化合物有(2S)-(4E)-N-甲基-5-[3-(5-异丙氧基-1-氧代吡啶)基)]-4-戊烯-2-胺，(3E)-N-甲基-4-(3-(1-氧代吡啶)基)-3-丁烯-1-胺，(4E)-N-甲基-5-(3-(1-氧代吡啶)基)-4-戊烯-2-胺，(4E)-N-甲基-5-(3-(5-((羧甲基)氧基)吡啶)基)-4-戊烯-2-胺，(3E)-N-甲基-4-[3-(5-硝基-6-氨基吡啶)基]-3-丁烯-1-胺，(3E)-N-甲基-4-[3-(5-(N-苯甲酰基)吡啶)基]-3-丁烯-1-胺，(4E)-N-甲基-5-[5-(2-氨基嘧啶)基]-4-戊烯-2-胺，(4E)-N-甲基-5-(3-(5-氨基吡啶)基)-4-戊烯-2-胺，(3E)-N-甲基-4-(3-(5-异丁氧基吡啶)基)-3-丁烯-1-胺，(3E)-N-甲基-4-(3-(5-乙硫基吡啶)基)-3-丁烯-1-胺，(4E)-N-甲基-5-(3-(5-三氟甲基吡啶)基)-4-戊烯-2-胺，(4E)-5-(3-(5-异丙氧基吡啶)基)-4-戊烯-2-胺，以及(4E)-5-(3-(5-异丙氧基吡啶)基)-4-戊烯-2-胺。
• Hydroxybenzoate salts of metanicotine compounds
  申请人：Munoz A. Julio

  公开号：US20060122237A1

  公开（公告）日：2006-06-08

  Patients susceptible to or suffering from conditions and disorders, such as central nervous system disorders, are treated by administering to a patient in need thereof compositions that are hydroxybenzoate salts of E-metanicotine-type compounds. The formation of hydroxybenzoate salts of the E-metanicotine compounds is also useful in purifying the E-metanicotine compounds, as the hydroxybenzoate salts tend to crystallize out, leaving impurities such as Z-metanicotine compounds, and compounds where the double bond has migrated, in solution. If desired, the hydroxybenzoate salts can be converted to either the free base (the E-metanicotine) or to another pharmaceutically acceptable salt form.

  易感或患有中枢神经系统疾病等状况的患者，通过向需要治疗的患者施用氢氧基苯酸盐型的E-甲基烟碱类化合物来进行治疗。形成E-甲基烟碱化合物的氢氧基苯酸盐也可用于纯化E-甲基烟碱化合物，因为氢氧基苯酸盐倾向于结晶出来，留下杂质，如Z-甲基烟碱化合物和双键迁移的化合物在溶液中。如果需要，氢氧基苯酸盐可以转化为自由基（E-甲基烟碱）或其他药学上可接受的盐形式。
• HYDROXYBENZOATE SALTS OF METANICOTINE COMPOUNDS
  申请人：Dull Gary Maurice

  公开号：US20080249142A1

  公开（公告）日：2008-10-09

  Patients susceptible to or suffering from conditions and disorders, such as central nervous system disorders, are treated by administering to a patient in need thereof compositions that are hydroxybenzoate salts of E-metanicotine-type compounds. The formation of hydroxybenzoate salts of the E-metanicotine compounds is also useful in purifying the E-metanicotine compounds, as the hydroxybenzoate salts tend to crystallize out, leaving impurities such as Z-metanicotine compounds, and compounds where the double bond has migrated, in solution. If desired, the hydroxybenzoate salts can be converted to either the free base (the E-metanicotine compound) or to another pharmaceutically acceptable salt form.

  易感受或患有中枢神经系统疾病等疾病和疾病的患者，通过给需要治疗的患者施用羟基苯甲酸盐型E-甲烟碱类化合物的组合物来治疗。形成羟基苯甲酸盐的E-甲烟碱化合物也有助于纯化E-甲烟碱化合物，因为羟基苯甲酸盐倾向于结晶出来，留下杂质，例如Z-甲烟碱化合物和双键迁移的化合物在溶液中。如有需要，羟基苯甲酸盐可转化为自由碱（E-甲烟碱化合物）或另一种药学上可接受的盐形式。
• Hydroxybenzoate Salts Of Metanicotine Compounds
  申请人：Munoz Julio A.

  公开号：US20090062321A1

  公开（公告）日：2009-03-05

  Patients susceptible to or suffering from conditions and disorders, such as central nervous system disorders, are treated by administering to a patient in need thereof compositions that are hydroxybenzoate salts of E-metanicotine-type compounds. The formation of hydroxybenzoate salts of the E-metanicotine compounds is also useful in purifying the E-metanicotine compounds, as the hydroxybenzoate salts tend to crystallize out, leaving impurities such as Z-metanicotine compounds, and compounds where the double bond has migrated, in solution. If desired, the hydroxybenzoate salts can be converted to either the free base (the E-metanicotine) or to another pharmaceutically acceptable salt form.

  对于易感受或患有中枢神经系统疾病等疾病和疾病的患者，可以通过向需要治疗的患者施用羟基苯甲酸酯盐的E-甲烟碱型化合物来进行治疗。羟基苯甲酸酯盐的形成对于纯化E-甲烟碱化合物也是有用的，因为羟基苯甲酸酯盐往往会结晶出来，留下杂质，例如Z-甲烟碱化合物和双键迁移的化合物。如果需要，羟基苯甲酸酯盐可以转化为自由碱基（E-甲烟碱）或其他药学上可接受的盐形式。