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1,4,6-trimethyl-N-(2-pyroolidin-1-ylethyl)-1,4-diazepan-6-amine | 1002789-60-7

中文名称
——
中文别名
——
英文名称
1,4,6-trimethyl-N-(2-pyroolidin-1-ylethyl)-1,4-diazepan-6-amine
英文别名
1,4,6-trimethyl-N-(2-(pyrrolidin-1-yl)ethyl)-1,4-diazepane-6-amine;1,4,6-trimethyl-N-(2-pyrrolidin-1-ylethyl)-1,4-diazepan-6-amine
1,4,6-trimethyl-N-(2-pyroolidin-1-ylethyl)-1,4-diazepan-6-amine化学式
CAS
1002789-60-7
化学式
C14H30N4
mdl
——
分子量
254.419
InChiKey
QULQWGKQVHLMAW-UHFFFAOYSA-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):
    0.4
  • 重原子数:
    18
  • 可旋转键数:
    4
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    21.8
  • 氢给体数:
    1
  • 氢受体数:
    4

反应信息

  • 作为反应物:
    描述:
    1,4,6-trimethyl-N-(2-pyroolidin-1-ylethyl)-1,4-diazepan-6-amine甲苯 为溶剂, 生成 (1,4,6-trimethyl-N-(2-(pyrrolidin-1-yl)ethyl)-1,4-diazepane-6-amine(-H))Sc(phenylacetylenide)2
    参考文献:
    名称:
    Scandium, Yttrium, and Lanthanum Benzyl and Alkynyl Complexes with the N-(2-Pyrrolidin-1-ylethyl)-1,4-diazepan-6-amido Ligand: Synthesis, Characterization, and Z-Selective Catalytic Linear Dimerization of Phenylacetylenes
    摘要:
    1,4,6-Trimethyl-N-(2-pyrrolidin-1-ylethyl)-1,4-diazepan-6-amine (HL) reacts with M(CH2Ph)(3)(THF)(3) to give the dibenzyl complexes (L)M(CH2Ph)(2) (M = SC, 1; M = Y, 2; M = La, 3). Compounds 1, 2, and 3 can be converted to their corresponding cationic monobenzyl species [(L)M(CH2Ph)](+) (M = Sc, Y and La) by reaction with [PhNMe2H][B(C6F5)(4)]. Reaction of (L)Sc(CH2Ph)(2) with 2 equiv of phenylacetylene affords the monomeric dialkynyl complex (L)Sc(C CPh)(2) (4), while reactions of (L)M(CH2Ph)(2) (M = Y and La) give the dimeric dialkynyl complexes [(L)M(C CPh)(mu-C CPh)](2) (M = Y, 5; M = La, 6). The neutral complexes (2, 3, 5, and 6) and the cationic monobenzyl species [(L)M(CH2Ph)](+) (M = Y and La) are catalysts for the Z-selective linear head-to-head dimerization of phenylacetylenes. The cationic yttrium and the neutral lanthanum systems are the most effective catalysts in the series. The related scandium species show poor activity and selectivity.
    DOI:
    10.1021/om8004228
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文献信息

  • Highly Efficient Regio- and Stereoselective Dimerization of (Hetero)aromatic Terminal Alkynes by Organo Rare-Earth Metal Catalysts
    作者:Shaozhong Ge、Victor F. Quiroga Norambuena、Bart Hessen
    DOI:10.1021/om700893f
    日期:2007.12.1
    4-diazepan-6-amine), activated by [PhNMe2H][B(C6F5)4], catalytically dimerizes a range of (hetero)aromatic alkynes to Z-enynes with 100% selectivity and high rates. Catalyst turnovers up to 2000 were readily achieved in preparative scale (5–10 mmol) reactions. For comparison, the related E-enynes were produced with a permethyl lanthanocene catalyst.
    钇二烷基络合物[(L)Y(CH 2 SiMe 3)2 ](1,L = 1,4,6-三甲基-N-(2-吡咯烷-1-基乙基)-1,4-二氮杂-6-胺)被[PhNMe 2 H] [B(C 6 F 5)4 ]活化,以100%的选择性和高速率将一系列(杂)芳族炔烃催化二聚为Z-烯炔。在制备规模(5-10 mmol)反应中,催化剂的周转量可轻松达到2000。为了进行比较,用全甲基镧系茂催化剂制备了相关的E-烯炔。
  • Scandium, Yttrium, and Lanthanum Benzyl and Alkynyl Complexes with the <i>N</i>-(2-Pyrrolidin-1-ylethyl)-1,4-diazepan-6-amido Ligand: Synthesis, Characterization, and <i>Z</i>-Selective Catalytic Linear Dimerization of Phenylacetylenes
    作者:Shaozhong Ge、Auke Meetsma、Bart Hessen
    DOI:10.1021/om8004228
    日期:2009.2.9
    1,4,6-Trimethyl-N-(2-pyrrolidin-1-ylethyl)-1,4-diazepan-6-amine (HL) reacts with M(CH2Ph)(3)(THF)(3) to give the dibenzyl complexes (L)M(CH2Ph)(2) (M = SC, 1; M = Y, 2; M = La, 3). Compounds 1, 2, and 3 can be converted to their corresponding cationic monobenzyl species [(L)M(CH2Ph)](+) (M = Sc, Y and La) by reaction with [PhNMe2H][B(C6F5)(4)]. Reaction of (L)Sc(CH2Ph)(2) with 2 equiv of phenylacetylene affords the monomeric dialkynyl complex (L)Sc(C CPh)(2) (4), while reactions of (L)M(CH2Ph)(2) (M = Y and La) give the dimeric dialkynyl complexes [(L)M(C CPh)(mu-C CPh)](2) (M = Y, 5; M = La, 6). The neutral complexes (2, 3, 5, and 6) and the cationic monobenzyl species [(L)M(CH2Ph)](+) (M = Y and La) are catalysts for the Z-selective linear head-to-head dimerization of phenylacetylenes. The cationic yttrium and the neutral lanthanum systems are the most effective catalysts in the series. The related scandium species show poor activity and selectivity.
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