phenyl-[(1S,9S,11R)-10-[(1S)-1-phenylethyl]-3,10-diazatetracyclo[6.4.1.04,13.09,11]trideca-4,6,8(13)-trien-3-yl]methanone | 132557-13-2

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 吲哚及其衍生物
• 英文名称: phenyl-[(1S,9S,11R)-10-[(1S)-1-phenylethyl]-3,10-diazatetracyclo[6.4.1.04,13.09,11]trideca-4,6,8(13)-trien-3-yl]methanone
• CAS: 132557-13-2；132619-32-0；141434-26-6
• 化学式: C₂₆H₂₄N₂O
• 分子量: 380.489
• InChiKey: JLCMJCUBVYDRFM-HBKJVLBKSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  5.32
• 重原子数：
  29.0
• 可旋转键数：
  3.0
• 环数：
  6.0
• sp3杂化的碳原子比例：
  0.27
• 拓扑面积：
  23.32
• 氢给体数：
  0.0
• 氢受体数：
  2.0

反应信息

• 作为反应物：
  描述：

  phenyl-[(1S,9S,11R)-10-[(1S)-1-phenylethyl]-3,10-diazatetracyclo[6.4.1.04,13.09,11]trideca-4,6,8(13)-trien-3-yl]methanone 在 palladium on activated charcoal 氢气 作用下， 以 溶剂黄146 为溶剂， 以30%的产率得到
  参考文献：
  名称：

  The synthesis of (+)- and (−)-1-benzoyl-1,2,2a,3,4,5-hexahydrobenz[cd]indol-4-amine, and preparation of LY228729.

  摘要：

  Racemic epoxide 5 was reacted with S-Phenylethylamine to afford diastereomers 6 and 7, from which amino alcohol 6 could be isolated directly. Aziridine formation and tandem-hydrogenolysis provided optically pure primary amine 2 (31% from racemic 4), which was further elaborated to LY228729 (15), an interesting 5HT1a receptor agonist.

  DOI：

  10.1016/s0040-4039(00)97303-9
• 作为产物：
  描述：

  [(2aR,4R,5R)-4-Hydroxy-5-((S)-1-phenyl-ethylamino)-2a,3,4,5-tetrahydro-2H-benzo[cd]indol-1-yl]-phenyl-methanone 在 三苯基膦 、 偶氮二甲酸二乙酯 作用下， 以 四氢呋喃 为溶剂， 以84.5%的产率得到phenyl-[(1S,9S,11R)-10-[(1S)-1-phenylethyl]-3,10-diazatetracyclo[6.4.1.04,13.09,11]trideca-4,6,8(13)-trien-3-yl]methanone
  参考文献：
  名称：

  Synthetic Studies toward the Partial Ergot Alkaloid LY228729, a Potent 5HT_1A Receptor Agonist

  摘要：

  Synthetic studies on LY228729 (3) afforded two innovative approaches for the construction of this class of partial ergoline 5HT(1a) receptor agonists. The first synthesis is based upon a diastereoselective epoxidation of racemic olefin 5, followed by ring opening and covalent resolution to furnish the key amino alcohol 8. Aziridination of amino alcohol 8, with subsequent tandem hydrogenolysis of the benzylic aziridine and auxiliary bonds, provided access to the optically active primary amine 13. A novel catalytic carboxamidation reaction installed the requisite side chain, Alternatively, the chiral pool was drawn upon for the single stereogenic center by virtue of L-tryptophan, albeit by a more circuitous route than expected. L-Tryptophan was differentially protected and reduced to the indoline diastereomers 26a,b which were separated by fractional crystallization. The two indoline diastereoisomers were independently cyclized by a Friedel-Crafts protocol, which under thermodynamic control afforded enantiomeric ketones 30a. The ketone was deoxygenated with a two-step reduction protocol to intersect the initial route and complete the second total synthesis. The two routes offer complementary access to this exciting class of partial ergot alkaloids.

  DOI：

  10.1021/jo971256z