tert-butyl N-[(3S)-2-oxo-1-(pyridin-4-ylmethyl)azepan-3-yl]carbamate | 643045-88-9

• 分子结构分类: 有机化合物 - 有机酸及其衍生物 - 羧酸及其衍生物
• 英文名称: tert-butyl N-[(3S)-2-oxo-1-(pyridin-4-ylmethyl)azepan-3-yl]carbamate
• CAS: 643045-88-9
• 化学式: C₁₇H₂₅N₃O₃
• 分子量: 319.404
• InChiKey: CVEWZUUCHXIEGL-AWEZNQCLSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.8
• 重原子数：
  23
• 可旋转键数：
  5
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.59
• 拓扑面积：
  71.5
• 氢给体数：
  1
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  tert-butyl N-[(3S)-2-oxo-1-(pyridin-4-ylmethyl)azepan-3-yl]carbamate 在 盐酸 、 三乙酰氧基硼氢化钠 作用下， 以 1,4-二氧六环 、 二氯甲烷 为溶剂， 生成
  参考文献：
  名称：

  Parallel liquid synthesis of N,N′-Disubstituted 3-amino azepin-2-ones as potent and specific farnesyl transferase inhibitors

  摘要：

  A rapid structure-activity study was performed by parallel liquid synthesis on N,N'-disubstitution of 3-amino azepin-2-one to afford potent and specific farnesyl transferase inhibitors with low nM enzymatic and cellular activities. The activities of the selected compounds were validated in vivo, and compounds 41a and 44a presented significant antitumour activity. (C) 2003 Elsevier Science Ltd. All rights reserved.

  DOI：

  10.1016/s0968-0896(03)00218-9
• 作为产物：
  描述：

  (S)-3-氨基-2-己内酰胺 在 sodium hydroxide 、 sodium hydride 作用下， 以 四氢呋喃 、 叔丁醇 为溶剂， 反应 13.08h， 生成 tert-butyl N-[(3S)-2-oxo-1-(pyridin-4-ylmethyl)azepan-3-yl]carbamate
  参考文献：
  名称：

  Parallel liquid synthesis of N,N′-Disubstituted 3-amino azepin-2-ones as potent and specific farnesyl transferase inhibitors

  摘要：

  A rapid structure-activity study was performed by parallel liquid synthesis on N,N'-disubstitution of 3-amino azepin-2-one to afford potent and specific farnesyl transferase inhibitors with low nM enzymatic and cellular activities. The activities of the selected compounds were validated in vivo, and compounds 41a and 44a presented significant antitumour activity. (C) 2003 Elsevier Science Ltd. All rights reserved.

  DOI：

  10.1016/s0968-0896(03)00218-9