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4-氨基-6-氯-2-二乙基氨基嘧啶 | 3289-38-1

中文名称
4-氨基-6-氯-2-二乙基氨基嘧啶
中文别名
——
英文名称
4-amino-6-chloro-2-diethylaminopyrimidine
英文别名
6-chloro-N2,N2-diethyl-pyrimidine-2,4-diamine;4-Amino-6-chlor-2-diaethylamino-pyrimidin;6-chloro-N2,N2-diethylpyrimidine-2,4-diamine;6-chloro-2-N,2-N-diethylpyrimidine-2,4-diamine
4-氨基-6-氯-2-二乙基氨基嘧啶化学式
CAS
3289-38-1
化学式
C8H13ClN4
mdl
MFCD09743981
分子量
200.671
InChiKey
XZIIFPSPUDAGJM-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):
    2
  • 重原子数:
    13
  • 可旋转键数:
    3
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.5
  • 拓扑面积:
    55
  • 氢给体数:
    1
  • 氢受体数:
    4

SDS

SDS:47872388339b5549ebc3200218862a07
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反应信息

  • 作为反应物:
    描述:
    二碳酸二叔丁酯4-氨基-6-氯-2-二乙基氨基嘧啶 在 sodium hydride 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 以85%的产率得到
    参考文献:
    名称:
    A practical strategy for the synthesis of 2-dialkylamino-4-arylamino-6-aminopyrimidines
    摘要:
    Starting from commercially available 4-amino-2,6-dichloropyrimidine, a practical four steps synthesis of 2-dialkylamino-4-arylamino-6-aminopyrimidines was developed. This strategy could introduce a diverse set of secondary amines and arylamines to displace the 2- and 4-chloro groups. The products of this route are otherwise difficult to access. In addition, 6-amino arylation was carried out to demonstrate the reactivity and utility of 2-dialkylamino-4-arylamino-6-aminopyrimidines as building blocks for assembling interesting aminopyrimidine molecules. (C) 2009 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetlet.2009.07.154
  • 作为产物:
    描述:
    4-氨基-2,6-二氯嘧啶二乙胺N,N-二异丙基乙胺 作用下, 以 异丙醇 为溶剂, 以90%的产率得到4-氨基-6-氯-2-二乙基氨基嘧啶
    参考文献:
    名称:
    A practical strategy for the synthesis of 2-dialkylamino-4-arylamino-6-aminopyrimidines
    摘要:
    Starting from commercially available 4-amino-2,6-dichloropyrimidine, a practical four steps synthesis of 2-dialkylamino-4-arylamino-6-aminopyrimidines was developed. This strategy could introduce a diverse set of secondary amines and arylamines to displace the 2- and 4-chloro groups. The products of this route are otherwise difficult to access. In addition, 6-amino arylation was carried out to demonstrate the reactivity and utility of 2-dialkylamino-4-arylamino-6-aminopyrimidines as building blocks for assembling interesting aminopyrimidine molecules. (C) 2009 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetlet.2009.07.154
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文献信息

  • Yellow Azo Dyes for Ink Jet Printing
    申请人:Wright Gavin
    公开号:US20100068472A1
    公开(公告)日:2010-03-18
    Monomers and dimers of mono-azo compounds of formula wherein: D is an optionally substituted aryl or an optionally substituted heteroaryl group; R 1 and R 2 are each independently optionally substituted alkyl: halo: amino: —NR 4 R 5 ; wherein R 4 is H, optionally substituted alkyl, optionally substituted alkoxy, optionally substituted acyl, optionally substituted aryl, optionally substituted heterocyclyl; and R 5 is optionally substituted alkyl, optionally substituted alkoxy, optionally substituted acyl, optionally substituted aryl, optionally substituted heterocyclyl or R 4 together with R 5 and the nitrogen to which they are attached forms an optionally substituted 5 or 6 membered ring: —OR 6 ; wherein R 6 is H or optionally substituted alkyl: or —SR 7 ; wherein R 7 is optionally substituted alkyl; R 3 is amino: halo; —NR 4 R 5 ; wherein R 4 is H, optionally substituted alkyl, optionally substituted alkoxy, optionally substituted acyl, optionally substituted aryl, optionally substituted heterocyclyl; and R 5 is optionally substituted alkyl, optionally substituted alkoxy, optionally substituted acyl, optionally substituted aryl, optionally substituted heterocyclyl or R 4 together with R 5 and the nitrogen to which they are attached forms an optionally substituted 5 or 6 membered ring: hydroxy: —OR 6 ; wherein R 6 is H or optionally substituted alkyl: or —SR 7 ; wherein R 7 is optionally substituted alkyl. Also compositions, inks and ink-jet cartridges containing these compounds and ink-jet printing processes using these compounds.
    单偶氮化合物的单体和二聚体,化学式如下:其中:D是可选择取代的芳基或可选择取代的杂环基;R1和R2各自独立地是可选择取代的烷基、卤素、氨基、-NR4R5;其中R4是H、可选择取代的烷基、可选择取代的烷氧基、可选择取代的酰基、可选择取代的芳基、可选择取代的杂环基;R5是可选择取代的烷基、可选择取代的烷氧基、可选择取代的酰基、可选择取代的芳基、可选择取代的杂环基或者R4和R5以及它们所连接的氮原子形成可选择取代的5或6元环;-OR6;其中R6是H或可选择取代的烷基;或-SR7;其中R7是可选择取代的烷基;R3是氨基、卤素、-NR4R5;其中R4是H、可选择取代的烷基、可选择取代的烷氧基、可选择取代的酰基、可选择取代的芳基、可选择取代的杂环基;R5是可选择取代的烷基、可选择取代的烷氧基、可选择取代的酰基、可选择取代的芳基、可选择取代的杂环基或者R4和R5以及它们所连接的氮原子形成可选择取代的5或6元环;羟基;-OR6;其中R6是H或可选择取代的烷基;或-SR7;其中R7是可选择取代的烷基。此外,还包括含有这些化合物的组合物、油墨和喷墨墨盒以及使用这些化合物的喷墨打印工艺。
  • Guillier, Fabrice; Roussel, Patrick; Moser, Heinz, Chemistry - A European Journal, 1999, vol. 5, # 12, p. 3450 - 3458
    作者:Guillier, Fabrice、Roussel, Patrick、Moser, Heinz、Kane, Peter、Bradley, Mark
    DOI:——
    日期:——
  • Hurst, Derek, T.; Johnson, Matthew, Heterocycles, 1985, vol. 23, # 3, p. 611 - 616
    作者:Hurst, Derek, T.、Johnson, Matthew
    DOI:——
    日期:——
  • HURST, D. T.;JOHNSON, M., HETEROCYCLES, 1985, 23, N 3, 611-616
    作者:HURST, D. T.、JOHNSON, M.
    DOI:——
    日期:——
  • Ink-Jet Printing Using Disazo Dyes
    申请人:James Rachel Anne
    公开号:US20090017278A1
    公开(公告)日:2009-01-15
    Compounds of Formula (1) and dimers thereof: wherein: A and B independently are optionally substituted aryl or optionally substituted heteroaryl groups; R 1 and R 2 are each independently optionally substituted alkyl: halo: amino: —NR 4 R 5 ; wherein R 4 is H, optionally substituted alkyl, optionally substituted alkoxy, optionally substituted acyl, optionally substituted aryl, optionally substituted heterocyclyl; and R 5 is optionally substituted alkyl, optionally substituted alkoxy, optionally substituted acyl, optionally substituted aryl, optionally substituted heterocyclyl or R 4 together with R 5 and the nitrogen to which they are attached forms an optionally substituted 5 or 6 membered ring: —OR 6 ; wherein R 6 is H or optionally substituted alkyl: or —SR 7 ; wherein R 7 is optionally substituted alkyl; R 3 is optionally substituted alkyl: halo: amino: —NR 4 R 5 ; wherein R 4 is H, optionally substituted alkyl, optionally substituted alkoxy, optionally substituted acyl, optionally substituted aryl, optionally substituted heterocyclyl; and R 5 is optionally substituted alkyl, optionally substituted alkoxy, optionally substituted acyl, optionally substituted aryl, optionally substituted heterocyclyl or R 4 together with R 5 and the nitrogen to which they are attached forms an optionally substituted 5 or 6 membered ring: —OR 6 ; wherein R 6 is H or optionally substituted alkyl: or —SR 7 ; wherein R 7 is optionally substituted alkyl; also ink-jet inks and processes and printed materials.
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