4-chloro-5-(ethyn-1-yl)-pyrrolo[2,3-d]pyrimidine | 865365-85-1

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 吡咯并嘧啶类
• 英文名称: 4-chloro-5-(ethyn-1-yl)-pyrrolo[2,3-d]pyrimidine
• 英文别名: 4-chloro-5-ethynyl-7H-pyrrolo[2,3-d]pyrimidine
• CAS: 865365-85-1
• 化学式: C₈H₄ClN₃
• 分子量: 177.593
• InChiKey: GQMQSKGUGDHONH-UHFFFAOYSA-N

物化性质

• 密度：
  1.50±0.1 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  1.9
• 重原子数：
  12
• 可旋转键数：
  1
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.0
• 拓扑面积：
  41.6
• 氢给体数：
  1
• 氢受体数：
  2

文献信息

• [EN] NEW ANTIVIRAL MODIFIED NUCLEOSIDES<br/>[FR] NOUVEAUX NUCLÉOSIDES MODIFIÉS ANTIVIRAUX
  申请人：NOVARTIS AG

  公开号：WO2010015643A1

  公开（公告）日：2010-02-11

  This invention relates to novel compounds that have various medicinal applications, e.g. for the treatment and/or prevention of viral infections. wherein: X is CH or CR6; R1 is halogen, NR7R8 or OR9; R2 is H, halogen, or NR7R8; R3 is H, alkyl, alkenyl, alkynyl, aryl, cycloalkyl, heterocycloalkyl or heteroaryl, each of which is optionally substituted with one or more substituents; R4 is H, acyl or an amino acid ester; R5 is H, acyl or an amino acid ester; R6 is alkyl, alkenyl, alkynyl, aryl, cycloalkyl, heterocycloalkyl, heteroaryl, halogen, cyano, nitro, hydroxy, alkoxy, alkylthio, amino, alkylamino, carboxy, carboxamide or alkyloxycarbonyl, each of which is optionally substituted with one or more substituents; R7 and R8 are independently selected from the group consisting of H, alkyl, alkenyl, alkynyl, aryl, cycloalkyl, heterocycloalkyl, heteroaryl, amino, alkylamino, arylamino, hydroxy, alkoxy, arylcarbonyl and alkylcarbonyl, each of which is optionally substituted with one or more substituents; and R3 is H, alkyl, alkenyl, alkynyl, aryl, cycloalkyl, heterocycloalkyl, heteroaryl, alkylcarbonyl or arylcarbonyl, each of which is optionally substituted with one or more substituents;

  这项发明涉及具有各种药用应用的新化合物，例如用于治疗和/或预防病毒感染。其中：X为CH或CR6；R1为卤素，NR7R8或OR9；R2为H，卤素或NR7R8；R3为H，烷基，烯基，炔基，芳基，环烷基，杂环烷基或杂芳基，每种均可选择性地被一个或多个取代基取代；R4为H，酰基或氨基酸酯；R5为H，酰基或氨基酸酯；R6为烷基，烯基，炔基，芳基，环烷基，杂环烷基，杂芳基，卤素，氰基，硝基，羟基，烷氧基，烷硫基，氨基，烷基氨基，羧基，羧酰胺或烷氧羰基，每种均可选择性地被一个或多个取代基取代；R7和R8分别选自H，烷基，烯基，炔基，芳基，环烷基，杂环烷基，杂芳基，氨基，烷基氨基，芳基氨基，羟基，烷氧基，芳基羰基和烷基羰基的群组，每种均可选择性地被一个或多个取代基取代；R3为H，烷基，烯基，炔基，芳基，环烷基，杂环烷基，杂芳基，烷基羰基或芳基羰基，每种均可选择性地被一个或多个取代基取代；
• Methods for preparing 7-(2'-substituted-beta-D-ribofuranosyl)-4-(NR2R3)-5-(substituted ethyn-1-yl)-pyrrolo[2,3-d]pyrimidine derivatives
  申请人：Roberts D. Christopher

  公开号：US20050215510A1

  公开（公告）日：2005-09-29

  Disclosed are methods and intermediates for the preparation of 7-(2′-R 1 -substituted-β-D-ribofuranosyl)-4-amino-5-(optionally substituted ethyn-1-yl)-pyrrolo[2,3-d]pyrimidine compounds. These compounds are useful in treating viral infections caused by a flaviviridae family virus, such as hepatitis C virus.

  本发明涉及制备7-(2'-R1-取代的β-D-核糖呋喃基)-4-氨基-5-(可选择取代的乙炔基)-吡咯并[2,3-d]嘧啶类化合物的方法和中间体。这些化合物可用于治疗由黄病毒科病毒引起的病毒感染，例如丙型肝炎病毒。
• NOVEL NUCLEOSIDE ANALOGS FOR TREATMENT OF VIRAL INFECTIONS
  申请人：Yin Zheng

  公开号：US20100227833A1

  公开（公告）日：2010-09-09

  This invention relates to novel compounds that have various medicinal applications, e.g. for the treatment and/or prevention of viral infections.

  本发明涉及一种具有各种药用应用的新化合物，例如用于治疗和/或预防病毒感染。
• ORGANIC COMPOUNDS
  申请人：CHEN Yen Liang

  公开号：US20100144655A1

  公开（公告）日：2010-06-10

  This invention relates to novel compounds that have various medicinal applications, e.g. for the treatment and/or prevention of viral infections.

  本发明涉及新型化合物，具有各种药物应用，例如用于治疗和/或预防病毒感染。
• METHODS FOR PREPARING 7-(2 -SUBSTITUTED-s-D-RIBOFURANO SYL)-4-(NR2R3)-5-(SUBSTITUTED ETHYN-1-YL)-PYRROLO 2,3-D|PYRIMIDINE DERIVATIVES
  申请人：GENELABS TECHNOLOGIES, INC.

  公开号：EP1682564A1

  公开（公告）日：2006-07-26