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(S)-[1-benzyl-2-(2-bromobenzyloxy)-ethyl]-(2-bromo-4,5-dimethoxy-benzyl)-methyl-amine | 286687-94-3

中文名称
——
中文别名
——
英文名称
(S)-[1-benzyl-2-(2-bromobenzyloxy)-ethyl]-(2-bromo-4,5-dimethoxy-benzyl)-methyl-amine
英文别名
(2S)-N-[(2-bromo-4,5-dimethoxyphenyl)methyl]-1-[(2-bromophenyl)methoxy]-N-methyl-3-phenylpropan-2-amine
(S)-[1-benzyl-2-(2-bromobenzyloxy)-ethyl]-(2-bromo-4,5-dimethoxy-benzyl)-methyl-amine化学式
CAS
286687-94-3
化学式
C26H29Br2NO3
mdl
——
分子量
563.329
InChiKey
ZYKRCXINNUEWOU-QFIPXVFZSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    6.5
  • 重原子数:
    32
  • 可旋转键数:
    11
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.31
  • 拓扑面积:
    30.9
  • 氢给体数:
    0
  • 氢受体数:
    4

上下游信息

  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    (S)-[1-benzyl-2-(2-bromobenzyloxy)-ethyl]-(2-bromo-4,5-dimethoxy-benzyl)-methyl-amine叔丁基锂1,3-二硝基苯 作用下, 以 various solvent(s) 为溶剂, 以92%的产率得到(S)-8-Benzyl-12,13-dimethoxy-9-methyl-7,8,9,10-tetrahydro-5H-6-oxa-9-aza-dibenzo[a,c]cyclodecene
    参考文献:
    名称:
    面向多样性、立体选择性合成含双芳基或双(芳基)金属的中环
    摘要:
    实验技术和装置除非另有说明,反应在氩气下用干燥的、新鲜蒸馏的溶剂进行。从钠/二苯甲酮羰基中蒸馏出四氢呋喃。无水 2-甲基四氢呋喃(Aldrich,外消旋)储存在活化的分子筛上。从氢化钙中蒸馏出二氯甲烷。正丁基锂的己烷溶液 (Aldrich) 和叔丁基锂的戊烷溶液 (Aldrich) 在使用前用 1,10 菲咯啉和无水 2-丁醇滴定。所有其他试剂均按照“实验室化学品的纯化”中的说明进行纯化或使用从商业来源获得的。产率是指色谱和光谱纯的化合物。所有反应均通过薄层色谱法 (TLC) 使用预涂有大肠杆菌的玻璃板进行监测。默克硅胶 60 F254 或氧化铝 60 F254。通过紫外荧光猝灭(λmax = 254nm)或用钼酸铈铵或 Dragendorff's 试剂(0.08% w/v 次硝酸铋和 2% w/v KI 的 3M aq. AcOH)染色进行可视化。保留因子 (Rf) 引用为 0.01。熔点是使用
    DOI:
    10.1021/ja0010507
  • 作为产物:
    描述:
    6-溴藜芦醛甲酸 、 sodium hydride 作用下, 以 四氢呋喃甲醇氯仿 为溶剂, 反应 5.5h, 生成 (S)-[1-benzyl-2-(2-bromobenzyloxy)-ethyl]-(2-bromo-4,5-dimethoxy-benzyl)-methyl-amine
    参考文献:
    名称:
    Diversity-Oriented Synthesis of Biaryl-Containing Medium Rings Using a One Bead/One Stock Solution Platform
    摘要:
    Diversity-oriented synthesis of structurally complex and diverse small molecules can be used as the first step in a process to explore cellular and organismal pathways. The success of this process is likely going to be dependent on advances in the synthesis of small molecules having natural product-like structures in an efficient and stereoselective manner. The development, scope, and mechanism of the oxidation of organocuprates was investigated and exploited in the atropdiastereoselective synthesis of biaryl-containing medium rings (9-, 10-, and 11-membered rings). The methodology was performed on high-capacity, large polystyrene beads by metalating aryl bromides with i-PrBu2MgLi, followed by transmetalating with CuCN.2LiBr and then oxidizing with 1,3-dinitrobenzene, and was used in a diversity-oriented synthesis of biaryl-containing medium rings (library total theoretical maximum 1412 members). The high capacity beads were arrayed into 384-well plates and, using a process optimized during the development of a one bead/one stock solution technology platform, converted into arrays of stock solutions, with each stock solution containing largely one compound. These stock solutions were used in numerous phenotypic and protein-binding assays. The process described outlines a pathway that we feel will contribute to a comprehensive and systematic chemical approach to exploring biology (chemical genetics).
    DOI:
    10.1021/ja017248o
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文献信息

  • Diversity-Oriented Synthesis of Biaryl-Containing Medium Rings Using a One Bead/One Stock Solution Platform
    作者:David R. Spring、Shyam Krishnan、Helen E. Blackwell、Stuart L. Schreiber
    DOI:10.1021/ja017248o
    日期:2002.2.1
    Diversity-oriented synthesis of structurally complex and diverse small molecules can be used as the first step in a process to explore cellular and organismal pathways. The success of this process is likely going to be dependent on advances in the synthesis of small molecules having natural product-like structures in an efficient and stereoselective manner. The development, scope, and mechanism of the oxidation of organocuprates was investigated and exploited in the atropdiastereoselective synthesis of biaryl-containing medium rings (9-, 10-, and 11-membered rings). The methodology was performed on high-capacity, large polystyrene beads by metalating aryl bromides with i-PrBu2MgLi, followed by transmetalating with CuCN.2LiBr and then oxidizing with 1,3-dinitrobenzene, and was used in a diversity-oriented synthesis of biaryl-containing medium rings (library total theoretical maximum 1412 members). The high capacity beads were arrayed into 384-well plates and, using a process optimized during the development of a one bead/one stock solution technology platform, converted into arrays of stock solutions, with each stock solution containing largely one compound. These stock solutions were used in numerous phenotypic and protein-binding assays. The process described outlines a pathway that we feel will contribute to a comprehensive and systematic chemical approach to exploring biology (chemical genetics).
  • Towards Diversity-Oriented, Stereoselective Syntheses of Biaryl- or Bis(aryl)metal-Containing Medium Rings
    作者:David R. Spring、Shyam Krishnan、Stuart L. Schreiber
    DOI:10.1021/ja0010507
    日期:2000.6.1
    FT-IR spectrometer with internal referencing. Absorption maxima (νmax) are reported in wavenumbers (cm) and the following abbreviations are used: w, weak; m, medium; s, strong; br, broad. Proton magnetic resonance spectra were recorded on Varian Mercury400 (400MHz), Bruker Avance DMX500 (500MHz), and Varian Unity/Inova500 (500MHz) spectrometers. Proton assignments are supported by H-H COSY, HMQC, NOESY
    实验技术和装置除非另有说明,反应在氩气下用干燥的、新鲜蒸馏的溶剂进行。从钠/二苯甲酮羰基中蒸馏出四氢呋喃。无水 2-甲基四氢呋喃(Aldrich,外消旋)储存在活化的分子筛上。从氢化钙中蒸馏出二氯甲烷。正丁基锂的己烷溶液 (Aldrich) 和叔丁基锂的戊烷溶液 (Aldrich) 在使用前用 1,10 菲咯啉和无水 2-丁醇滴定。所有其他试剂均按照“实验室化学品的纯化”中的说明进行纯化或使用从商业来源获得的。产率是指色谱和光谱纯的化合物。所有反应均通过薄层色谱法 (TLC) 使用预涂有大肠杆菌的玻璃板进行监测。默克硅胶 60 F254 或氧化铝 60 F254。通过紫外荧光猝灭(λmax = 254nm)或用钼酸铈铵或 Dragendorff's 试剂(0.08% w/v 次硝酸铋和 2% w/v KI 的 3M aq. AcOH)染色进行可视化。保留因子 (Rf) 引用为 0.01。熔点是使用
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