benzoic acid 4-dimethylamino-2-[4-ethyl-1-(4-indol-1-yl-butyl)-11-methoxy-7,9,11,13,15-pentamethyl-2,6,8,14-tetraoxo-tetradecahydro-3,5-dioxa-1-aza-cyclopentacyclotetradecen-10-yloxy]-6-methyl-tetrahydro-pyran-3-yl ester | 484672-10-8

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: benzoic acid 4-dimethylamino-2-[4-ethyl-1-(4-indol-1-yl-butyl)-11-methoxy-7,9,11,13,15-pentamethyl-2,6,8,14-tetraoxo-tetradecahydro-3,5-dioxa-1-aza-cyclopentacyclotetradecen-10-yloxy]-6-methyl-tetrahydro-pyran-3-yl ester
• CAS: 484672-10-8
• 化学式: C₄₉H₆₇N₃O₁₁
• 分子量: 874.084
• InChiKey: UCXACRPORXZOPW-HHGROVHVSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  7.1
• 重原子数：
  63.0
• 可旋转键数：
  12.0
• 环数：
  6.0
• sp3杂化的碳原子比例：
  0.61
• 拓扑面积：
  152.14
• 氢给体数：
  0.0
• 氢受体数：
  13.0

反应信息

• 作为反应物：
  描述：

  benzoic acid 4-dimethylamino-2-[4-ethyl-1-(4-indol-1-yl-butyl)-11-methoxy-7,9,11,13,15-pentamethyl-2,6,8,14-tetraoxo-tetradecahydro-3,5-dioxa-1-aza-cyclopentacyclotetradecen-10-yloxy]-6-methyl-tetrahydro-pyran-3-yl ester 在 甲醇 作用下， 反应 22.0h， 生成 (1S,2R,5R,7R,8R,9R,11R,13R,14R)-8-[(2S,3R,4S,6R)-4-(dimethylamino)-3-hydroxy-6-methyloxan-2-yl]oxy-2-ethyl-15-(4-indol-1-ylbutyl)-9-methoxy-5,7,9,11,13-pentamethyl-3,17-dioxa-15-azabicyclo[12.3.0]heptadecane-4,6,12,16-tetrone
  参考文献：
  名称：

  Synthesis and antibacterial activity of C12 des-methyl ketolides

  摘要：

  Synthesis of C-12 des-methyl ketolide is developed featuring an intramolecular epoxide formation/elimination process to establish the C-12 stereocenter. These ketolides are potent against several key respiratory pathogens, including erythromycin resistant erm- and mef-containing strains of Streptococcus pneumoniae. (c) 2006 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2006.05.104
• 作为产物：
  描述：

  [(2S,3R,4S,6R)-2-[[(1R,3R,6R,7S,8S,9R,10R,12R,13S,17S)-7-[(2R,4R,5S,6S)-5-benzoyloxy-4-methoxy-4,6-dimethyloxan-2-yl]oxy-3-ethyl-10-methoxy-6,8,10,12,15,15,17-heptamethyl-2-methylidene-5-oxo-4,14,16-trioxabicyclo[11.3.1]heptadecan-9-yl]oxy]-4-(dimethylamino)-6-methyloxan-3-yl] benzoate 在 盐酸 、 4-二甲氨基吡啶 、 sodium tetrahydroborate 、 sodium hydride 、 戴斯-马丁氧化剂 、 对甲苯磺酸 、 臭氧 、 1,8-二氮杂双环[5.4.0]十一碳-7-烯 、 三乙胺 作用下， 以 四氢呋喃 、 甲醇 、 乙醇 、 二氯甲烷 、 乙腈 为溶剂， 反应 135.26h， 生成 benzoic acid 4-dimethylamino-2-[4-ethyl-1-(4-indol-1-yl-butyl)-11-methoxy-7,9,11,13,15-pentamethyl-2,6,8,14-tetraoxo-tetradecahydro-3,5-dioxa-1-aza-cyclopentacyclotetradecen-10-yloxy]-6-methyl-tetrahydro-pyran-3-yl ester
  参考文献：
  名称：

  Synthesis and antibacterial activity of C12 des-methyl ketolides

  摘要：

  Synthesis of C-12 des-methyl ketolide is developed featuring an intramolecular epoxide formation/elimination process to establish the C-12 stereocenter. These ketolides are potent against several key respiratory pathogens, including erythromycin resistant erm- and mef-containing strains of Streptococcus pneumoniae. (c) 2006 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2006.05.104