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5,6-dimethyl-3-(pyridin-4-yl)-1,2,4-triazine | 115486-16-3

中文名称
——
中文别名
——
英文名称
5,6-dimethyl-3-(pyridin-4-yl)-1,2,4-triazine
英文别名
5,6-dimethyl-3-(4-pyridinyl)-1,2,4-triazine;5,6-dimethyl-3-[4]pyridyl-[1,2,4]triazine;5,6-Dimethyl-3-[4]pyridyl-[1,2,4]triazin;5,6-dimethyl-3-pyridin-4-yl-1,2,4-triazine
5,6-dimethyl-3-(pyridin-4-yl)-1,2,4-triazine化学式
CAS
115486-16-3
化学式
C10H10N4
mdl
MFCD06617777
分子量
186.216
InChiKey
GMJLTZBWZUYHCJ-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):
    0.6
  • 重原子数:
    14
  • 可旋转键数:
    1
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.2
  • 拓扑面积:
    51.6
  • 氢给体数:
    0
  • 氢受体数:
    4

反应信息

  • 作为反应物:
    描述:
    5,6-dimethyl-3-(pyridin-4-yl)-1,2,4-triazinesodium hydroxidepotassium permanganate 作用下, 反应 22.0h, 以61%的产率得到1,6-dihydro-6-oxo-3-(4-pyridinyl)-1,2,4-triazine-5-carboxylic acid
    参考文献:
    名称:
    Synthesis of Aza Analogs of Amrinone
    摘要:
    The aldol condensation product (4) of 4-acetylpyridine (2) and diethyl mesoxalate (3) was converted to pyridazinecarboxylic acid hydrazide (6). Curtius reaction of 6 gave aminopyridazinone (7). The condensation of (4-pyridinyl)glyoxal (17) with aminomalonamide (9) yielded pyrazinecarboxamide (18) which was transformed to aminopyrazinone (19) by the Hofmann reaction. Curtius reaction of 1,2,4-triazinone-5-carboxylic acid (21b) gave aminotriazinone (22). Demethylation of methoxypyrimidine (29) prepared from methyl 2-methoxyformylacetate (25) and isonicotinamidine (26) gave pyrimidinol (30).
    DOI:
    10.3987/com-90-5562
  • 作为产物:
    描述:
    异烟肼2,3-丁二酮N,N,N’,N’-tetrabromobenzene-1,3-disulfonamide 、 ammonium acetate 作用下, 以 neat (no solvent) 为溶剂, 反应 3.05h, 以87%的产率得到5,6-dimethyl-3-(pyridin-4-yl)-1,2,4-triazine
    参考文献:
    名称:
    使用N-卤代磺酰胺无溶剂合成三嗪†
    摘要:
    在这项研究中,N,N,N ',N'-四溴苯-1,3-二磺酰胺和聚(N-溴-N-乙基苯-1,3-二磺酰胺)被用作有效的催化剂,一锅法合成了苯胺。 3,5,6-三取代-1,2,4-三嗪来自于100°C易得的酰肼,乙酸铵和二羰基化合物,在无溶剂条件下产率高至优异。
    DOI:
    10.1039/c4ra10892b
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文献信息

  • Metze, Chemische Berichte, 1956, vol. 89, p. 2056,2057,2059
    作者:Metze
    DOI:——
    日期:——
  • SINGH, BALVED;LESHER, GEOGRE Y., HETEROCYCLES, 31,(1990) N2, C. 2163-2172
    作者:SINGH, BALVED、LESHER, GEOGRE Y.
    DOI:——
    日期:——
  • Synthesis of Aza Analogs of Amrinone
    作者:Baldev Singh、George Y. Lesher
    DOI:10.3987/com-90-5562
    日期:——
    The aldol condensation product (4) of 4-acetylpyridine (2) and diethyl mesoxalate (3) was converted to pyridazinecarboxylic acid hydrazide (6). Curtius reaction of 6 gave aminopyridazinone (7). The condensation of (4-pyridinyl)glyoxal (17) with aminomalonamide (9) yielded pyrazinecarboxamide (18) which was transformed to aminopyrazinone (19) by the Hofmann reaction. Curtius reaction of 1,2,4-triazinone-5-carboxylic acid (21b) gave aminotriazinone (22). Demethylation of methoxypyrimidine (29) prepared from methyl 2-methoxyformylacetate (25) and isonicotinamidine (26) gave pyrimidinol (30).
  • Solvent-free synthesis of triazines using N-halosulfonamides
    作者:Ramin Ghorbani-Vaghei、Azadeh Shahriari、Zahra Salimi、Somayeh Hajinazari
    DOI:10.1039/c4ra10892b
    日期:——
    In this study, N,N,N′,N-tetrabromobenzene-1,3-disulfonamide and poly(N-bromo-N-ethylbenzene-1,3-disulfonamide) were used as efficient catalysts for the one-pot synthesis of 3,5,6-trisubstituted-1,2,4-triazines from readily available acid hydrazides, ammonium acetate and dicarbonyl compounds at 100 °C in good to excellent yields under solvent-free conditions.
    在这项研究中,N,N,N ',N'-四溴苯-1,3-二磺酰胺和聚(N-溴-N-乙基苯-1,3-二磺酰胺)被用作有效的催化剂,一锅法合成了苯胺。 3,5,6-三取代-1,2,4-三嗪来自于100°C易得的酰肼,乙酸铵和二羰基化合物,在无溶剂条件下产率高至优异。
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