2,3,6,7-tetrahydro-9-(methyl-tert-butoxycarbonylamino)-1H,5H,11H-[1]benzopyrano[6,7,8-ij]quinolizin-11-one | 1386264-17-0

• 分子结构分类: 有机化合物 - 苯丙烷和聚酮 - 香豆素及其衍生物
• 英文名称: 2,3,6,7-tetrahydro-9-(methyl-tert-butoxycarbonylamino)-1H,5H,11H-[1]benzopyrano[6,7,8-ij]quinolizin-11-one
• 英文别名: tert-butyl N-[(4-oxo-3-oxa-13-azatetracyclo[7.7.1.02,7.013,17]heptadeca-1(17),2(7),5,8-tetraen-6-yl)methyl]carbamate
• CAS: 1386264-17-0
• 化学式: C₂₁H₂₆N₂O₄
• 分子量: 370.448
• InChiKey: YPICANGKDZHDQK-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.9
• 重原子数：
  27
• 可旋转键数：
  4
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.52
• 拓扑面积：
  67.9
• 氢给体数：
  1
• 氢受体数：
  5

反应信息

• 作为产物：
  描述：

  8-(2,3,6,7-tetrahydro-1H,5H-benzo[ij]quinolizine) 4-(tert-butoxycarbonylamino)but-2-ynoate 在 silver hexafluoroantimonate 、 三苯基膦氯金 作用下， 以 1,4-二氧六环 、 1,2-二氯乙烷 为溶剂， 以90%的产率得到2,3,6,7-tetrahydro-9-(methyl-tert-butoxycarbonylamino)-1H,5H,11H-[1]benzopyrano[6,7,8-ij]quinolizin-11-one
  参考文献：
  名称：

  Catalytic Coupling of Arene C–H Bonds and Alkynes for the Synthesis of Coumarins: Substrate Scope and Application to the Development of Neuroimaging Agents

  摘要：

  C-H bond functionalization offers strategically novel approaches to complex organic compounds. However, many C-H functionalization reactions suffer from poor compatibility with Lewis basic functional groups, especially amines, which are often essential for biological activity. This study describes a systematic examination of the substrate scope of catalytic hydroarylation in the context of complex amino coumarin synthesis. The choice of substrates was guided by the design and development of the next generation of fluorescent false neurotransmitters (FFNs), neuroimaging probes we recently introduced for optical imaging of neurotransmission in the brain. Comparison of two mild protocols using catalytic PtCl4 or Au(PPh3)Cl/AgSbF6 revealed that each method has a broad and mutually complementary substrate scope. The relatively less active platinum system out-performed the gold catalyst with indole substrates lacking substitution at the C-3 position and provided higher regioselectivity in the case of carbazole-based substrates. On the other hand, the more active gold catalyst demonstrated excellent functional group tolerance, and the ability to catalyze the formation of strained, helical products. The development of these two protocols offers enhanced substrate scope and provides versatile synthetic tools required for the structure-activity examination of FFN neuroimaging probes as well as for the synthesis of complex coumarins in general.

  DOI：

  10.1021/jo3006842