<1aS,8S,8(1a'S,8'S,8a'S,8b'R),8a'S,8b'R>-1a,1a',8,8',8a,8a',8b,8b'-Octahydro-<8,8'-bi-8H-azirino<2',3':3,4>pyrrolo<1,2-a>indole>-8,8'-dicarbonitrile | 159763-78-7

• 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: <1aS,8S,8(1a'S,8'S,8a'S,8b'R),8a'S,8b'R>-1a,1a',8,8',8a,8a',8b,8b'-Octahydro-<8,8'-bi-8H-azirino<2',3':3,4>pyrrolo<1,2-a>indole>-8,8'-dicarbonitrile
• 英文别名: (1aS,8S,8(1a'S,8'S,8a'S,8b'R),8a'S,8b'R)-1a,1a',8,8',8a,8a',8b,8b'-Octahydro-(8,8'-bi-8H-azirino[2',3':3,4]pyrrolo[1,2-a]indole)-8,8'-dicarbonitrile；tert-butyl (4S,6R,7S,8S)-8-cyano-8-[(4S,6R,7S,8S)-8-cyano-5-[(2-methylpropan-2-yl)oxycarbonyl]-2,5-diazatetracyclo[7.4.0.02,7.04,6]trideca-1(13),9,11-trien-8-yl]-2,5-diazatetracyclo[7.4.0.02,7.04,6]trideca-1(13),9,11-triene-5-carboxylate
• CAS: 159763-78-7
• 化学式: C₃₄H₃₆N₆O₄
• 分子量: 592.698
• InChiKey: QEIQYEZECSWUFE-OHSKPEKVSA-N

物化性质

• 沸点：
  745.498±60.00 °C(Press: 760.00 Torr)(predicted)
• 密度：
  1.423±0.10 g/cm3(Temp: 25 °C; Press: 760 Torr)(predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  3.7
• 重原子数：
  44
• 可旋转键数：
  5
• 环数：
  8.0
• sp3杂化的碳原子比例：
  0.53
• 拓扑面积：
  113
• 氢给体数：
  0
• 氢受体数：
  8

反应信息

• 作为反应物：
  描述：

  <1aS,8S,8(1a'S,8'S,8a'S,8b'R),8a'S,8b'R>-1a,1a',8,8',8a,8a',8b,8b'-Octahydro-<8,8'-bi-8H-azirino<2',3':3,4>pyrrolo<1,2-a>indole>-8,8'-dicarbonitrile 以 四氢呋喃 为溶剂， 反应 3.5h， 以37%的产率得到tert-butyl (4S,6R,7S,8R)-8-cyano-2,5-diazatetracyclo[7.4.0.02,7.04,6]trideca-1(13),9,11-triene-5-carboxylate
  参考文献：
  名称：

  Cyclization of Chiral Carbon-Centered Aziridinyl Radicals: A New Route to Azirino[2',3':3,4]pyrrolo[1,2-a]indoles

  摘要：

  A carbon-centered aziridinyl radical has been generated from the ester of chiral aziridine carboxylic acid 5b. The resultant radical has been cyclized directly and has been brominated with CBrCl3. The bromo aziridines have also been cyclized reductively in the presence of n-Bu(3)SnH. Dihydroindole 8b bears the same relative and absolute stereochemistry as the mitomycin C nucleus.

  DOI：

  10.1021/jo00105a009
• 作为产物：
  描述：

  3-氰基吲哚 在 lithium hydroxide 、 三丁基膦 、 sodium hexamethyldisilazane 作用下， 以 四氢呋喃 、 二氯甲烷 为溶剂， 反应 9.0h， 生成 <1aS,8S,8(1a'S,8'S,8a'S,8b'R),8a'S,8b'R>-1a,1a',8,8',8a,8a',8b,8b'-Octahydro-<8,8'-bi-8H-azirino<2',3':3,4>pyrrolo<1,2-a>indole>-8,8'-dicarbonitrile
  参考文献：
  名称：

  Cyclization of Chiral Carbon-Centered Aziridinyl Radicals: A New Route to Azirino[2',3':3,4]pyrrolo[1,2-a]indoles

  摘要：

  A carbon-centered aziridinyl radical has been generated from the ester of chiral aziridine carboxylic acid 5b. The resultant radical has been cyclized directly and has been brominated with CBrCl3. The bromo aziridines have also been cyclized reductively in the presence of n-Bu(3)SnH. Dihydroindole 8b bears the same relative and absolute stereochemistry as the mitomycin C nucleus.

  DOI：

  10.1021/jo00105a009

文献信息

• Cyclization of Chiral Carbon-Centered Aziridinyl Radicals: A New Route to Azirino[2',3':3,4]pyrrolo[1,2-a]indoles
  作者：Frederick E. Ziegler、Makonen Belema

  DOI：10.1021/jo00105a009

  日期：1994.12

  A carbon-centered aziridinyl radical has been generated from the ester of chiral aziridine carboxylic acid 5b. The resultant radical has been cyclized directly and has been brominated with CBrCl3. The bromo aziridines have also been cyclized reductively in the presence of n-Bu(3)SnH. Dihydroindole 8b bears the same relative and absolute stereochemistry as the mitomycin C nucleus.