N1-allyl-N10,N10-dimethyltryptamine

• 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: N1-allyl-N10,N10-dimethyltryptamine
• 英文别名: N,N-dimethyl-2-(1-prop-2-enylindol-3-yl)ethanamine
• 化学式: C₁₅H₂₀N₂
• 分子量: 228.337
• InChiKey: RRJWWOJZCZAVFM-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3
• 重原子数：
  17
• 可旋转键数：
  5
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.33
• 拓扑面积：
  8.2
• 氢给体数：
  0
• 氢受体数：
  1

反应信息

• 作为反应物：
  描述：

  N1-allyl-N10,N10-dimethyltryptamine 在 1,3-bis[(diphenylphosphino)propane]dichloronickel(II) 二异丁基氢化铝 作用下， 以 甲苯 为溶剂， 反应 2.0h， 以0.19 g的产率得到N,N-二甲基色胺
  参考文献：
  名称：

  通过阴离子苯并环化合成功能化的吲哚和苯并稠合的杂环衍生物。

  摘要：

  报道了一种新的方法的发展，该方法用于区域选择性合成功能化的吲哚和六元苯并稠合的N，O和S杂环。关键步骤涉及生成苯并炔系链的乙烯基或芳基锂化合物，该化合物随后进行分子内阴离子环化。有机锂中间体与选择的亲电试剂的反应使得可以制备多种吲哚，四氢咔唑，二氢苯并吡啶，二苯并吡喃和二苯并噻喃并吡喃衍生物。最后，将该策略应用于合适的起始原料可以制备一些色胺和5-羟色胺类似物。

  DOI：

  10.1002/1521-3765(20020503)8:9<2034::aid-chem2034>3.0.co;2-i
• 作为产物：
  描述：

  N1-allyl-N10-methyl-N10-Boc-tryptamine 在 三氟乙酸 作用下， 以 甲醇 、 二氯甲烷 为溶剂， 反应 4.5h， 生成 N1-allyl-N10,N10-dimethyltryptamine
  参考文献：
  名称：

  Synthesis and evaluation of N1-alkylindole-3-ylalkylammonium compounds as nicotinic acetylcholine receptor ligands

  摘要：

  In this study thirty-three novel indole derivatives were designed and synthesized based on the structure of deformylflustrabromine B (1), a metabolite isolated from the marine bryozoan Flustra foliacea L. The syntheses were carried out using standard methodologies and in good yields. The molecules were tested for their affinities for the alpha 4 beta 2*, alpha 3 beta 4*, alpha 7* and (alpha 1)(2)beta 1 gamma delta nicotinic acetylcholine receptor (nAChR) sub-types. Binding assays showed that, among these ligands, compound 7c exhibited the highest affinity with K-i = 136.1, 93.9 and 862.4 nM for the alpha 4 beta 2*, alpha 3 beta 4*, and alpha 7* nAChRs subtypes, respectively. These results indicated that the indole core might be a useful scaffold for the development of new potent and selective nAChR ligands. (C) 2012 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmc.2012.04.050

文献信息

• Synthesis and evaluation of N1-alkylindole-3-ylalkylammonium compounds as nicotinic acetylcholine receptor ligands
  作者：Edwin G. Pérez、Bruce K. Cassels、Christoph Eibl、Daniela Gündisch

  DOI：10.1016/j.bmc.2012.04.050

  日期：2012.6

  In this study thirty-three novel indole derivatives were designed and synthesized based on the structure of deformylflustrabromine B (1), a metabolite isolated from the marine bryozoan Flustra foliacea L. The syntheses were carried out using standard methodologies and in good yields. The molecules were tested for their affinities for the alpha 4 beta 2*, alpha 3 beta 4*, alpha 7* and (alpha 1)(2)beta 1 gamma delta nicotinic acetylcholine receptor (nAChR) sub-types. Binding assays showed that, among these ligands, compound 7c exhibited the highest affinity with K-i = 136.1, 93.9 and 862.4 nM for the alpha 4 beta 2*, alpha 3 beta 4*, and alpha 7* nAChRs subtypes, respectively. These results indicated that the indole core might be a useful scaffold for the development of new potent and selective nAChR ligands. (C) 2012 Elsevier Ltd. All rights reserved.
• Synthesis of Functionalized Indole- and Benzo-Fused Heterocyclic Derivatives through Anionic Benzyne Cyclization
  作者：José Barluenga、Francisco J. Fañanás、Roberto Sanz、Yolanda Fernández

  DOI：10.1002/1521-3765(20020503)8:9<2034::aid-chem2034>3.0.co;2-i

  日期：2002.5.3

  six-membered benzo-fused N-, O-, and S-heterocycles is reported. The key step involves the generation of a benzyne-tethered vinyl or aryllithium compound that undergoes a subsequent intramolecular anionic cyclization. Reaction of the organolithium intermediates with selected electrophiles allows the preparation of a wide variety of indole, tetrahydrocarbazole, dihydrofenantridine, dibenzopyran, and dibenzothiopyran

  报道了一种新的方法的发展，该方法用于区域选择性合成功能化的吲哚和六元苯并稠合的N，O和S杂环。关键步骤涉及生成苯并炔系链的乙烯基或芳基锂化合物，该化合物随后进行分子内阴离子环化。有机锂中间体与选择的亲电试剂的反应使得可以制备多种吲哚，四氢咔唑，二氢苯并吡啶，二苯并吡喃和二苯并噻喃并吡喃衍生物。最后，将该策略应用于合适的起始原料可以制备一些色胺和5-羟色胺类似物。