N-[9-[(2R,5R)-4-[bis(4-methoxyphenyl)-phenylmethoxy]-5-(hydroxymethyl)oxolan-2-yl]purin-6-yl]benzamide

• 分子结构分类: 有机化合物 - 苯类化合物 - 三苯基化合物
• 英文名称: N-[9-[(2R,5R)-4-[bis(4-methoxyphenyl)-phenylmethoxy]-5-(hydroxymethyl)oxolan-2-yl]purin-6-yl]benzamide
• 化学式: C₃₈H₃₅N₅O₆
• 分子量: 657.7
• InChiKey: LFXBQKFIXWICJR-HCMUIWFFSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.8
• 重原子数：
  49
• 可旋转键数：
  11
• 环数：
  7.0
• sp3杂化的碳原子比例：
  0.21
• 拓扑面积：
  130
• 氢给体数：
  2
• 氢受体数：
  9

文献信息

• Method for purifying 5' -protected 2' -deoxypurine nucleosides
  申请人：——

  公开号：US20030009028A1

  公开（公告）日：2003-01-09

  A method for efficiently purifying 5′ protected 2′-deoxypurine nucleosides, efficient production of which has previously been difficult. Impurities can be separated by obtaining the 5′ protected 2′-deoxypurine nucleoside as an inclusion crystal including a solvent such as that having a nitrile structure in order to purify the 5′ protected 2′-deoxypurine nucleoside at a high purity. This invention enables synthesis of highly purified protected deoxypurine nucleosides easily on a large scale, which has previously been performed by column chromatography method.

  一种用于高效纯化5′保护的2′-去氧嘌呤核苷的方法，先前其高效生产曾经困难。通过获得含有类似腈结构的溶剂的包含晶体，可将杂质分离以纯化5′保护的2′-去氧嘌呤核苷。该发明使得在大规模上轻松合成高纯度的保护去氧嘌呤核苷成为可能，而此前通常通过柱层析法进行。
• Method for purifying 5'-protected 2'-deoxypurine nucleosides
  申请人：Mitsui Chemicals, Inc.

  公开号：EP1253154B1

  公开（公告）日：2009-09-02
• US6958391B2
  申请人：——

  公开号：US6958391B2

  公开（公告）日：2005-10-25
• US7074917B2
  申请人：——

  公开号：US7074917B2

  公开（公告）日：2006-07-11