3-O-ethoxymethyl-17α-[2-(2-hydroxyethyl)benzyl]-17β-estradiol | 352196-29-3

• 分子结构分类: 有机化合物 - 脂质和类脂质分子 - 类固醇和类固醇衍生物
• 英文名称: 3-O-ethoxymethyl-17α-[2-(2-hydroxyethyl)benzyl]-17β-estradiol
• 英文别名: (8R,9S,13S,14S,17R)-3-(ethoxymethoxy)-17-[[2-(2-hydroxyethyl)phenyl]methyl]-13-methyl-7,8,9,11,12,14,15,16-octahydro-6H-cyclopenta[a]phenanthren-17-ol
• CAS: 352196-29-3
• 化学式: C₃₀H₄₀O₄
• 分子量: 464.645
• InChiKey: ZMGFXRUXDNCEMX-IXYVTWBDSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  5.9
• 重原子数：
  34
• 可旋转键数：
  8
• 环数：
  5.0
• sp3杂化的碳原子比例：
  0.6
• 拓扑面积：
  58.9
• 氢给体数：
  2
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  3-O-ethoxymethyl-17α-[2-(2-hydroxyethyl)benzyl]-17β-estradiol 在 偶氮二甲酸二异丙酯 、 三苯基膦 作用下， 以 苯 为溶剂， 反应 3.0h， 以15%的产率得到(4R,8'R,9'S,13'S,14'S)-3'-(ethoxymethoxy)-13'-methylspiro[2,5-dihydro-1H-3-benzoxepine-4,17'-7,8,9,11,12,14,15,16-octahydro-6H-cyclopenta[a]phenanthrene]
  参考文献：
  名称：

  Synthesis of functionalised enantiopure steroids from estrone and cholestanone through organolithium intermediates

  摘要：

  The reaction of epoxides I and 8 derived from estrone and cholestanone, respectively. with an excess of lithium and a catalytic amount of DTBB (7 mol%) in THF at -78 degreesC led to formation of the correlsponding beta -oxido-functionalised organolithium intermediates 2 and 9, respectively, in a regio- and stereoselective manner. Treatment of these intermediates with different electrophiles [H2O, D2O, PhCHO, Me2CO, Et2CO, (CH2)(5)CO, CO2] at -78 to 20 degreesC afforded, after hydrolysis with water. enantiomerically purr derivatives 3 and 10. respectively. When protected ketones 5 and 6 derived from D-glucose and D-fructose were used as the electrophile. the reaction with 2 gave the expected mixed products 3g and 3h, respectively. which consist of a steroid and a carbohydrate fragment. The fraction of O-protected estrone 4 as the electrophilic component and intermediate 2 afforded the C-2-symmetric steroid dimer 3f. The stereochemistry of the products was unambiguously determined by correlation with X-ray data for compound 3d and by comparison with the known compound 6a. Finally. thr addition of the dianions 13, resulting from the DTBB-catalysed lithiation of phthalan 12a and isochroman 12b, to the O-protected estrone 4 and to cholestanone 9 led to the Formation of the diols 14, 15 and 16. Diols 14 were cyclised under Mitsunobu reaction conditions to the corresponding heterocycles 17. (C) 2001 Elsevier Science Ltd. All rights reserved.

  DOI：

  10.1016/s0957-4166(01)00121-5
• 作为产物：
  描述：

  异色满 、 3-O-(ethoxymethyl)estrone 在 4,4'-二叔丁基苯并 、 lithium 作用下， 以 四氢呋喃 为溶剂， 反应 0.67h， 以30%的产率得到3-O-ethoxymethyl-17α-[2-(2-hydroxyethyl)benzyl]-17β-estradiol
  参考文献：
  名称：

  Synthesis of functionalised enantiopure steroids from estrone and cholestanone through organolithium intermediates

  摘要：

  The reaction of epoxides I and 8 derived from estrone and cholestanone, respectively. with an excess of lithium and a catalytic amount of DTBB (7 mol%) in THF at -78 degreesC led to formation of the correlsponding beta -oxido-functionalised organolithium intermediates 2 and 9, respectively, in a regio- and stereoselective manner. Treatment of these intermediates with different electrophiles [H2O, D2O, PhCHO, Me2CO, Et2CO, (CH2)(5)CO, CO2] at -78 to 20 degreesC afforded, after hydrolysis with water. enantiomerically purr derivatives 3 and 10. respectively. When protected ketones 5 and 6 derived from D-glucose and D-fructose were used as the electrophile. the reaction with 2 gave the expected mixed products 3g and 3h, respectively. which consist of a steroid and a carbohydrate fragment. The fraction of O-protected estrone 4 as the electrophilic component and intermediate 2 afforded the C-2-symmetric steroid dimer 3f. The stereochemistry of the products was unambiguously determined by correlation with X-ray data for compound 3d and by comparison with the known compound 6a. Finally. thr addition of the dianions 13, resulting from the DTBB-catalysed lithiation of phthalan 12a and isochroman 12b, to the O-protected estrone 4 and to cholestanone 9 led to the Formation of the diols 14, 15 and 16. Diols 14 were cyclised under Mitsunobu reaction conditions to the corresponding heterocycles 17. (C) 2001 Elsevier Science Ltd. All rights reserved.

  DOI：

  10.1016/s0957-4166(01)00121-5