4-chloro-5-methyl-2-(6-methylpyridin-2-yl)thieno[2,3-d]pyrimidine | 733806-84-3

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 二嗪类
• 英文名称: 4-chloro-5-methyl-2-(6-methylpyridin-2-yl)thieno[2,3-d]pyrimidine
• CAS: 733806-84-3
• 化学式: C₁₃H₁₀ClN₃S
• 分子量: 275.761
• InChiKey: QRWPWYKSJMCLIV-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.9
• 重原子数：
  18
• 可旋转键数：
  1
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.15
• 拓扑面积：
  66.9
• 氢给体数：
  0
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  4-chloro-5-methyl-2-(6-methylpyridin-2-yl)thieno[2,3-d]pyrimidine 、 3-苯基-1-丙胺 在 N,N-二异丙基乙胺 作用下， 以 1,4-二氧六环 为溶剂， 反应 3.0h， 以88%的产率得到5-methyl-2-(6-methylpyridin-2-yl)-N-(3-phenylpropyl)thieno[2,3-d]pyrimidin-4-amine
  参考文献：
  名称：

  [EN] THIENO[2,3-D)PYRIMIDINES AND BENZOFURO(3,2-D)PYRIMIDINES AS ANTIMICROBIAL AGENTS
  [FR] THIÉNO[2,3-D]PYRIMIDINES ET BENZOFURO(3,2-D) PYRIMIDINES UTILES EN TANT QU'AGENTS ANTIMICROBIENS

  摘要：

  本公开提供了可用于治疗结核病的化合物、方法和组合物。在某些实施例中，这些化合物和组合物具有对结核分枝杆菌（Mtb）具有杀菌作用的特性。还提供了使用这些药剂的方法。

  公开号：

  WO2019018359A1
• 作为产物：
  描述：

  5-methyl-2-(6-methylpyridin-2-yl)-3H-thieno[2,3-d]pyrimidin-4-one 在 三氯氧磷 作用下， 以 甲苯 为溶剂， 生成 4-chloro-5-methyl-2-(6-methylpyridin-2-yl)thieno[2,3-d]pyrimidine
  参考文献：
  名称：

  Design of novel quinazoline derivatives and related analogues as potent and selective ALK5 inhibitors

  摘要：

  Starting from quinazoline 3a, we designed potent and selective ALK5 inhibitors over p38MAP kinase from a rational drug design approach based on co-crystal structures in the human ALK5 kinase domain. The quinazoline 3d exhibited also in vivo activity in an acute rat model of DMN-induced liver fibrosis when administered orally at 5 mg/kg (bid). (c) 2009 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2009.02.087

文献信息

• [EN] NOVEL MICROBICIDES<br/>[FR] NOUVEAUX MICROBICIDES
  申请人：SYNGENTA PARTICIPATIONS AG

  公开号：WO2011104183A1

  公开（公告）日：2011-09-01

  Compounds of formula (I) wherein G1 represents together with the two ring atoms of the pyrimidine ring to which it is attached, a 5-to 6-membered aromatic heterocyclic ring system which contains one or two heteroatoms selected from the group consisting of nitrogen, oxygen and sulfur, and the other substituents are as defined in claim 1, are suitable for use as microbiocides.

  式(I)的化合物中，其中G1与连接它的嘧啶环的两个环原子一起表示一个含有氮、氧和硫中的一种或两种杂原子的5到6元芳香杂环环系，其它取代基如权利要求1所定义的那样，适用于用作微生物杀灭剂。
• NOVEL MICROBICIDES
  申请人：Pouliot Martin

  公开号：US20120316184A1

  公开（公告）日：2012-12-13

  Compounds of formula (I) wherein G 1 represents together with the two ring atoms of the pyrimidine ring to which it is attached, a 5- to 6-membered aromatic heterocyclic ring system which contains one or two heteroatoms selected from the group consisting of nitrogen, oxygen and sulfur, and the other substituents are as defined in claim 1 , are suitable for use as micro-biocides.

  化合物的式（I），其中G1表示与连接它的嘧啶环的两个环原子一起形成一个含有一个或两个从氮、氧和硫组成的杂原子的5-至6-成员芳香杂环系统，而其他取代基如权利要求1所定义的适用于作为微生物杀剂。
• THIENO[2,3-D)PYRIMIDINES AND BENZOFURO(3,2-D)PYRIMIDINES AS ANTIMICROBIAL AGENTS
  申请人：Saint Louis University

  公开号：US20220117968A1

  公开（公告）日：2022-04-21

  The present disclosure provides compounds, methods, and compositions which may be used to treat tuberculosis. In some embodiments, these compounds and compositions have a bactericidal property against Mycobacterium tuberculosis (Mtb). Methods of employing such agents are also provided.