(S,S)-1,3,4,5,7,8,10,11,12,13-decahydro-4-(ethoxycarbonyl)-8,10,10,13,13-pentamethyl-7-(1-methylethyl)-6H-benzo<1,4>diazonino<7,6,5-cd>indol-6-one | 134288-25-8

• 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: (S,S)-1,3,4,5,7,8,10,11,12,13-decahydro-4-(ethoxycarbonyl)-8,10,10,13,13-pentamethyl-7-(1-methylethyl)-6H-benzo<1,4>diazonino<7,6,5-cd>indol-6-one
• 英文别名: (S,S)-1,3,4,5,7,8,10,11,12,13-decahydro-4-(ethoxycarbonyl)-8,10,10,13,13-pentamethyl-7-(1-methylethyl)-6H-benzo[g][1,4]diazonino(7,6,5-cd)indol-6-one；ethyl (6S,9S)-10,14,14,17,17-pentamethyl-8-oxo-9-propan-2-yl-2,7,10-triazatetracyclo[9.7.1.04,19.013,18]nonadeca-1(18),3,11(19),12-tetraene-6-carboxylate
• CAS: 134288-25-8；134357-67-8
• 化学式: C₂₇H₃₉N₃O₃
• 分子量: 453.625
• InChiKey: ITVNIVWUSOKOKY-MBSDFSHPSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  6.4
• 重原子数：
  33
• 可旋转键数：
  4
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.63
• 拓扑面积：
  74.4
• 氢给体数：
  2
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  (S,S)-1,3,4,5,7,8,10,11,12,13-decahydro-4-(ethoxycarbonyl)-8,10,10,13,13-pentamethyl-7-(1-methylethyl)-6H-benzo<1,4>diazonino<7,6,5-cd>indol-6-one 在 锂硼氢 作用下， 以 四氢呋喃 为溶剂， 反应 3.0h， 以95%的产率得到(S,S)-1,3,4,5,7,8,10,11,12,13-decahydro-4-(hydroxymethyl)-8,10,10,13,13-pentamethyl-7-(1-methylethyl)-6H-benzo<1,4>diazonino<7,6,5-cd>indol-6-one
  参考文献：
  名称：

  Synthesis of a tetramethyl analog of teleocidin

  摘要：

  A simplified tetramethyl analogue 3 of Teleocidin B-4 (1) has been synthesized from dinitrotoluene 6 via indole 4. The valine moiety of analogue 3 was provided by the coupling of (N-methylamino)indole 16 derived from 4 with the triflate of (R)-2-hydroxyvaleric acid benzyl ester, and the tryptophanyl portion was constructed by alkylation of the resulting (S)-N-valylindole 17 with ethyl (3-bromo-2-oximido)propionate to give the oxime 18. After reduction to the diastereomeric amines 20 and 21, closure to the 9-membered lactam-esters 24 and 23 (respectively) was accomplished using BOP. Separation and reduction of the esters led to teleocidin analogue 3 and its epimeric alcohol 25, respectively.

  DOI：

  10.1021/jo00015a026
• 作为产物：
  描述：

  1,2,3,4-tetrahydro-1,1,4,4,6-pentamethyl-5,7-dinitronaphthalene 在 palladium on activated charcoal 2,6-二甲基吡啶 、 lithium aluminium tetrahydride 、 tris(triphenylphosphine)ruthenium(II) chloride 、 苄基三甲基氢氧化铵 、 铁粉 、 碳酸氢钠 、 sodium carbonate 、 溶剂黄146 、 环己烯 作用下， 以 四氢呋喃 、 乙醇 、 二氯甲烷 、 二甲基亚砜 、 1,2-二氯乙烷 、 甲苯 为溶剂， 反应 55.5h， 生成 (S,S)-1,3,4,5,7,8,10,11,12,13-decahydro-4-(ethoxycarbonyl)-8,10,10,13,13-pentamethyl-7-(1-methylethyl)-6H-benzo<1,4>diazonino<7,6,5-cd>indol-6-one
  参考文献：
  名称：

  Synthesis of a tetramethyl analog of teleocidin

  摘要：

  A simplified tetramethyl analogue 3 of Teleocidin B-4 (1) has been synthesized from dinitrotoluene 6 via indole 4. The valine moiety of analogue 3 was provided by the coupling of (N-methylamino)indole 16 derived from 4 with the triflate of (R)-2-hydroxyvaleric acid benzyl ester, and the tryptophanyl portion was constructed by alkylation of the resulting (S)-N-valylindole 17 with ethyl (3-bromo-2-oximido)propionate to give the oxime 18. After reduction to the diastereomeric amines 20 and 21, closure to the 9-membered lactam-esters 24 and 23 (respectively) was accomplished using BOP. Separation and reduction of the esters led to teleocidin analogue 3 and its epimeric alcohol 25, respectively.

  DOI：

  10.1021/jo00015a026

文献信息

• WEBB, ROBERT R. (II);VENUTI, MICHAEL C.;EIGENBROT, CHARLES, J. ORG. CHEM., 56,(1991) N5, C. 4706-4713
  作者：WEBB, ROBERT R. (II)、VENUTI, MICHAEL C.、EIGENBROT, CHARLES

  DOI：——

  日期：——
• Synthesis of a tetramethyl analog of teleocidin
  作者：Robert R. Webb、Michael C. Venuti、Charles Eigenbrot

  DOI：10.1021/jo00015a026

  日期：1991.7

  A simplified tetramethyl analogue 3 of Teleocidin B-4 (1) has been synthesized from dinitrotoluene 6 via indole 4. The valine moiety of analogue 3 was provided by the coupling of (N-methylamino)indole 16 derived from 4 with the triflate of (R)-2-hydroxyvaleric acid benzyl ester, and the tryptophanyl portion was constructed by alkylation of the resulting (S)-N-valylindole 17 with ethyl (3-bromo-2-oximido)propionate to give the oxime 18. After reduction to the diastereomeric amines 20 and 21, closure to the 9-membered lactam-esters 24 and 23 (respectively) was accomplished using BOP. Separation and reduction of the esters led to teleocidin analogue 3 and its epimeric alcohol 25, respectively.