(5-甲基咪唑并[1,2-a]吡啶-3-基)甲醇 | 178488-39-6

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 咪唑并吡啶类
• 中文名称: (5-甲基咪唑并[1,2-a]吡啶-3-基)甲醇
• 中文别名: (5-甲基咪唑并[1,2-A]吡啶-3-基)甲醇
• 英文名称: 5-methylimidazo[1,2-a]pyridin-3-yl methanol
• 英文别名: (5-Methylimidazo[1,2-a]pyridin-3-yl)methanol
• CAS: 178488-39-6
• 化学式: C₉H₁₀N₂O
• mdl: MFCD09864459
• 分子量: 162.191
• InChiKey: MVDFZQQVFPAFCJ-UHFFFAOYSA-N

物化性质

• 密度：
  1.22±0.1 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  1.3
• 重原子数：
  12
• 可旋转键数：
  1
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.222
• 拓扑面积：
  37.5
• 氢给体数：
  1
• 氢受体数：
  2

安全信息

• WGK Germany：
  3
• 危险性防范说明：
  P261,P280
• 危险性描述：
  H317
• 储存条件：
  存储条件：室温、密封、干燥。

反应信息

• 作为反应物：
  描述：

  (5-甲基咪唑并[1,2-a]吡啶-3-基)甲醇 在 氯化亚砜 作用下， 生成 3-氯甲基-5-甲基咪唑并[1,2-a]吡啶
  参考文献：
  名称：

  Synthesis of Acyclo-C-nucleosides in the Imidazo[1,2-a]pyridine and Pyrimidine Series as Antiviral Agents

  摘要：

  The synthesis and the antiviral activities of C-3 acyclic nucleoside analogues of imidazo[1,2-a]pyridine and pyrimidine are reported. From these compounds, 20, 21, 22, 23, 28, and 34 showed a specific activity against cytomegalovirus and/or varicella-zoster virus.

  DOI：

  10.1021/jm9507901
• 作为产物：
  描述：

  5-甲基咪唑并[1,2-a]吡啶 在 sodium tetrahydroborate 、 三氯氧磷 作用下， 以 甲醇 为溶剂， 生成 (5-甲基咪唑并[1,2-a]吡啶-3-基)甲醇
  参考文献：
  名称：

  Synthesis of Acyclo-C-nucleosides in the Imidazo[1,2-a]pyridine and Pyrimidine Series as Antiviral Agents

  摘要：

  The synthesis and the antiviral activities of C-3 acyclic nucleoside analogues of imidazo[1,2-a]pyridine and pyrimidine are reported. From these compounds, 20, 21, 22, 23, 28, and 34 showed a specific activity against cytomegalovirus and/or varicella-zoster virus.

  DOI：

  10.1021/jm9507901

文献信息

• BENZAZEPINE DERIVATIVE, PROCESS FOR PRODUCING THE SAME, AND USE
  申请人：Takeda Chemical Industries, Ltd.

  公开号：EP1422228A1

  公开（公告）日：2004-05-26

  The present invention provides a novel benzazepine derivative represented by formula : wherein, R1 is a 5- or 6-membered aromatic ring, R2 is lower alkyl group, etc., Y is an optionally substituted imino group, ring A and ring B are independently an optionally substituted aromatic ring, W is formula -W1-X2-W2- (W1 and W2 are independently S(O)m1 (m1 is 0, 1 or 2), etc., and X2 is an optionally substituted alkylene groupetc. ), a preparation method and use thereof.

  本发明提供了一种新型的苯并氮杂环衍生物，其由以下公式表示： 其中，R1是一个5-或6-成员的芳香环，R2是低级烷基团等，Y是可选地取代的亚氨基，环A和环B是独立地选自一个可选地取代的芳香环，W是公式-W1-X2-W2-（W1和W2是独立地为S(O)m1（m1是0、1或2）等，X2是一个可选地取代的亚烷基团等），其制备方法及其用途。
• Benzazepine derivative, process for producing the same, and use
  申请人：——

  公开号：US20040235822A1

  公开（公告）日：2004-11-25

  The present invention provides a novel benzazepine derivative represented by formula: 1 wherein, R 1 is a 5- or 6-membered aromatic ring, R 2 is lower alkyl group, etc., Y is an optionally substituted imino group, ring A and ring B are independently an optionally substituted aromatic ring, W is formula —W 1 —X 2 —W 2 — (W 1 and W 2 are independently S(O) m1 (m1 is 0, 1, or 2), etc., and X 2 is an optionally substituted alkylene group etc.), a preparation method and use thereof.

  本发明提供了一种新型苯并氮杂环衍生物，其化学式表示为：1其中，R1为5-或6-成员芳香环，R2为低碳基，Y为可选取代的亚胺基，环A和环B分别为可选取代的芳香环，W为式—W1—X2—W2—（其中W1和W2分别为独立的S(O)m1（m1为0、1或2）等，X2为可选取代的烷基等），以及其制备方法和用途。
• Benzimidazolone as potent chymase inhibitor: Modulation of reactive metabolite formation in the hydrophobic (P1) region
  作者：Ho Yin Lo、Peter A. Nemoto、Jin Mi Kim、Ming-Hong Hao、Kevin C. Qian、Neil A. Farrow、Daniel R. Albaugh、Danielle M. Fowler、Richard D. Schneiderman、E. Michael August、Leslie Martin、Melissa Hill-Drzewi、Steven S. Pullen、Hidenori Takahashi、Stéphane De Lombaert

  DOI：10.1016/j.bmcl.2011.05.126

  日期：2011.8

  A new class of chymase inhibitor featuring a benzimidazolone core with an acid side chain and a P-1 hydrophobic moiety is described. Incubation of the lead compound with GSH resulted in the formation of a GSH conjugate on the benzothiophene P-1 moiety. Replacement of the benzothiophene with different heterocyclic systems such as indoles and benzoisothiazole is feasible. Among the P-1 replacements, benzoisothiazole prevents the formation of GSH conjugate and an in silico analysis of oxidative potentials agreed with the experimental outcome. (C) 2011 Elsevier Ltd. All rights reserved.
• US7262185B2
  申请人：——

  公开号：US7262185B2

  公开（公告）日：2007-08-28
• Synthesis of Acyclo-<i>C</i>-nucleosides in the Imidazo[1,2-<i>a</i>]pyridine and Pyrimidine Series as Antiviral Agents
  作者：Alain Gueiffier、Mohammed Lhassani、Ahmed Elhakmaoui、Robert Snoeck、Graciela Andrei、Olivier Chavignon、Jean-Claude Teulade、Abdelali Kerbal、El Mokhtar Essassi、Jean-Claude Debouzy、Myriam Witvrouw、Yves Blache、Jan Balzarini、Erik De Clercq、Jean-Pierre Chapat

  DOI：10.1021/jm9507901

  日期：1996.1.1

  The synthesis and the antiviral activities of C-3 acyclic nucleoside analogues of imidazo[1,2-a]pyridine and pyrimidine are reported. From these compounds, 20, 21, 22, 23, 28, and 34 showed a specific activity against cytomegalovirus and/or varicella-zoster virus.