Pyrrolidinyl-acetylenic thieno[3,2-d]pyrimidine, 6j | 833476-36-1

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 噻吩并嘧啶酮衍生物
• 英文名称: Pyrrolidinyl-acetylenic thieno[3,2-d]pyrimidine, 6j
• 英文别名: [(3R,5S)-5-[2-[4-[3-chloro-4-[(3-fluorophenyl)methoxy]anilino]thieno[3,2-d]pyrimidin-6-yl]ethynyl]pyrrolidin-3-yl] N-(2-methylsulfonylethyl)carbamate
• CAS: 833476-36-1
• 化学式: C₂₉H₂₇ClFN₅O₅S₂
• 分子量: 644.147
• InChiKey: NWDMCJXGXJGDKM-IFMALSPDSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.5
• 重原子数：
  43
• 可旋转键数：
  11
• 环数：
  5.0
• sp3杂化的碳原子比例：
  0.28
• 拓扑面积：
  168
• 氢给体数：
  3
• 氢受体数：
  11

反应信息

• 作为产物：
  描述：

  tert-butyl (2S,4R)-2-((4-((3-chloro-4-((3-fluorobenzyl)oxy)phenyl)amino)thieno[3,2-d]pyrimidin-6-yl)ethynyl)-4-(((2-(methylsulfonyl)ethyl)carbamoyl)oxy)pyrrolidine-1-carboxylate 在 三氟乙酸 作用下， 以 二氯甲烷 为溶剂， 以90%的产率得到Pyrrolidinyl-acetylenic thieno[3,2-d]pyrimidine, 6j
  参考文献：
  名称：

  Synthesis and stereochemical effects of pyrrolidinyl-acetylenic thieno[3,2-d]pyrimidines as EGFR and ErbB-2 inhibitors

  摘要：

  A novel class of pyrrolidinyl-acetyleneic thieno[3,2-d]pyrimidines has been identified which potently inhibit the EGFR and ErbB-2 receptor tyrosine kinases. Synthetic modifications of the pyrrolidine carbamate moiety result in a range of effects on enzyme and cellular potency. In addition, the impact of the absolute stereochemical configuration on cellular potency and oral mouse pharmacokinetics is described. (C) 2008 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2008.11.023

文献信息

• Synthesis and stereochemical effects of pyrrolidinyl-acetylenic thieno[3,2-d]pyrimidines as EGFR and ErbB-2 inhibitors
  作者：Kirk L. Stevens、Krystal J. Alligood、Jennifer G. Badiang Alberti、Thomas R. Caferro、Stanley D. Chamberlain、Scott H. Dickerson、Hamilton D. Dickson、Holly K. Emerson、Robert J. Griffin、Robert D. Hubbard、Barry R. Keith、Robert J. Mullin、Kimberly G. Petrov、Roseanne M. Gerding、Michael J. Reno、Tara R. Rheault、David W. Rusnak、Douglas M. Sammond、Stephon C. Smith、David E. Uehling、Alex G. Waterson、Edgar R. Wood

  DOI：10.1016/j.bmcl.2008.11.023

  日期：2009.1

  A novel class of pyrrolidinyl-acetyleneic thieno[3,2-d]pyrimidines has been identified which potently inhibit the EGFR and ErbB-2 receptor tyrosine kinases. Synthetic modifications of the pyrrolidine carbamate moiety result in a range of effects on enzyme and cellular potency. In addition, the impact of the absolute stereochemical configuration on cellular potency and oral mouse pharmacokinetics is described. (C) 2008 Elsevier Ltd. All rights reserved.