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1-N-trityl-1,2,3,6-tetrahydropyridine | 73962-46-6

中文名称
——
中文别名
——
英文名称
1-N-trityl-1,2,3,6-tetrahydropyridine
英文别名
1-(Triphenylmethyl)-1,2,3,6-tetrahydropyridine;1-trityl-3,6-dihydro-2H-pyridine
1-N-trityl-1,2,3,6-tetrahydropyridine化学式
CAS
73962-46-6
化学式
C24H23N
mdl
——
分子量
325.453
InChiKey
RHEHGMVJJSEEBZ-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):
    5.6
  • 重原子数:
    25
  • 可旋转键数:
    4
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.17
  • 拓扑面积:
    3.2
  • 氢给体数:
    0
  • 氢受体数:
    1

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为产物:
    描述:
    参考文献:
    名称:
    The synthesis of piperidine nucleoside analogs—a comparison of several methods to access the introduction of nucleobases
    摘要:
    This work deals with the synthesis of piperidine and hydroxypiperidine analogs of nucleosides. Starting from commercially available 3-hydroxypiperidine, proline or 4-hydroxyproline, a series of piperidine derivatives of both purine and pyrimidine nucleobases was prepared. Various methods of nucleobase attachment were evaluated. The prepared compounds were tested for cytostatic, antibacterial, and antiviral properties but no significant activity was found. (C) 2010 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tet.2010.12.029
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文献信息

  • Cyclic amine derivative having heteroaryl ring
    申请人:Kimura Tomio
    公开号:US20060270706A1
    公开(公告)日:2006-11-30
    A compound having the general formula (I) wherein R 1 represents C1-C6 alkyl, etc., R 2 represents hydrogen, C2-C7 alkanoyl, C7-C11 arylcarbonyl, the formula R 4 —(CH 2 ) 1 —, etc., R 3 represents C6-C10 aryl, etc., X 1 , X 2 , X 3 , X 4 and X 5 each independently represents hydrogen, halogen, etc., and n represents an integer of 0 to 2, pharmacologically acceptable salts thereof or prodrugs thereof. They have excellent inhibition of platelet activation, etc. and are useful as a prophylactic or therapeutic agents for diseases related to thrombus or embolus formation.
    化合物具有通式(I),其中R1代表C1-C6烷基等,R2代表氢,C2-C7酰基,C7-C11芳基羰基,公式R4 -(CH2)1-等,R3代表C6-C10芳基等,X1,X2,X3,X4和X5各自独立地代表氢,卤素等,n代表0到2的整数,其药学上可接受的盐或前药。它们具有优异的抑制血小板活化等作用,并可用作与血栓或栓塞形成有关的疾病的预防或治疗剂。
  • The synthesis of piperidine nucleoside analogs—a comparison of several methods to access the introduction of nucleobases
    作者:Soňa Kovačková、Martin Dračínský、Dominik Rejman
    DOI:10.1016/j.tet.2010.12.029
    日期:2011.2
    This work deals with the synthesis of piperidine and hydroxypiperidine analogs of nucleosides. Starting from commercially available 3-hydroxypiperidine, proline or 4-hydroxyproline, a series of piperidine derivatives of both purine and pyrimidine nucleobases was prepared. Various methods of nucleobase attachment were evaluated. The prepared compounds were tested for cytostatic, antibacterial, and antiviral properties but no significant activity was found. (C) 2010 Elsevier Ltd. All rights reserved.
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