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2-[(5,7-dimethyl-6-oxo-4a,7a-diphenyl-4,4a,5,6,7,7a-hexahydro-1H-imidazo[4,5-e][1,2,4]triazin-3-yl)thio]acetic acid | 309290-75-3

中文名称
——
中文别名
——
英文名称
2-[(5,7-dimethyl-6-oxo-4a,7a-diphenyl-4,4a,5,6,7,7a-hexahydro-1H-imidazo[4,5-e][1,2,4]triazin-3-yl)thio]acetic acid
英文别名
{(5,7-dimethyl-6-oxo-4a,7a-diphenyl-4,4a,5,6,7,7a-hexahydro-1H-imidazo[4,5-e]-1,2,4-triazin-3-yl)thio}acetic acid;2-[(5,7-dimethyl-6-oxo-4a,7a-diphenyl-1,2-dihydroimidazo[4,5-e][1,2,4]triazin-4-ium-3-yl)sulfanyl]acetate
2-[(5,7-dimethyl-6-oxo-4a,7a-diphenyl-4,4a,5,6,7,7a-hexahydro-1H-imidazo[4,5-e][1,2,4]triazin-3-yl)thio]acetic acid化学式
CAS
309290-75-3
化学式
C20H21N5O3S
mdl
——
分子量
411.484
InChiKey
IXDQUBPMBWHEDW-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:
    29
  • 可旋转键数:
    5
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.25
  • 拓扑面积:
    123
  • 氢给体数:
    3
  • 氢受体数:
    6

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
  • 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:
    2-[(5,7-dimethyl-6-oxo-4a,7a-diphenyl-4,4a,5,6,7,7a-hexahydro-1H-imidazo[4,5-e][1,2,4]triazin-3-yl)thio]acetic acid乙酸酐 作用下, 反应 0.5h, 以83%的产率得到1,3-dimethyl-3a,9a-diphenyl-3,3a,9,9a-tetrahydroimidazo[4,5-e]-1,3-thiazolo[3,2-b]-1,2,4-triazine-2,7(1H,6H)-dione
    参考文献:
    名称:
    Condensation of 5,7-dimethyl-4a,7a-diphenyl-3-thioxoperhydroimidazo[4,5-e]-1,2,4-triazin-6-one with halogenoacetic acids
    摘要:
    The reaction of 5,7-dimethyl-4a,7a-diphenyl-3-thioxoperhydroimidazo[4,5-e]-1,2,4-triazin-6-one with halogenoacetic acids was studied, and the directed synthesis of {(5,7-dimethyl-6-oxo-4a,7a-diphenyl-4,4a,5,6,7,7a-hexahydro-1H-imidazo[4,5-e]-1,2,4-triazin-3-yl)thio} acetic acid and 1,3-dimethyl-3a,9a-diphenyl-3,3a,9,9a-tetrahydroimidazo[4,5-e]-1,3-thiazolo[3,2-b]-1,2,4-triazine-2,7(1H,6H)-dione was perfomed for the first time; the structures of title compounds were confirmed by the (1)H-{(13)C} HMBC, (1)H-{(15)N} HSQC, TOCSY, NOESY, HMBC, HSQCED NMR spectroscopy methods and XRD analysis of the tricyclic product.
    DOI:
    10.1016/j.mencom.2010.01.018
  • 作为产物:
    描述:
    盐酸 作用下, 以89%的产率得到2-[(5,7-dimethyl-6-oxo-4a,7a-diphenyl-4,4a,5,6,7,7a-hexahydro-1H-imidazo[4,5-e][1,2,4]triazin-3-yl)thio]acetic acid
    参考文献:
    名称:
    通过[3,2-b]-稠合异构体的骨架重排合成7-oxindolylidene-3a,9a-二苯基咪唑并噻唑并[2,3-c][1,2,4]三嗪
    摘要:
    以前无法获得的 7-oxindolylidene-1,3-dimethyl-3a,9adiphenylimidazo[4,5- e ]thiazolo[2,3 - c ][1,2,4]triazines 通过骨架脒重排获得 63-90% 的产率用甲醇钠处理相应的咪唑并[4,5 -e ]噻唑并[3,2- b ][1,2,4]三嗪中的噻唑三嗪体系。
    DOI:
    10.1016/j.mencom.2022.09.037
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文献信息

  • Transformations of S-substituted 5,7-dimethyl-4а,5а-diphenyl-3-thioxoperhydroimidazo[4,5-e]-1,2,4-triazin-2-ones under treatment of 1,2-benzoquinones and photochemical properties of reaction products
    作者:Angelina N. Kravchenko、Sergei V. Vasilevskii、Galina A. Gazieva、Vladimir V. Baranov、Valery A. Barachevsky、Olga I. Kobeleva、Olga V. Venidiktova、Valentina A. Karnoukhova
    DOI:10.1016/j.tet.2018.03.056
    日期:2018.5
    were prepared by the reactions of 3-alkylthio-5,7-dimethyl-4a,7a-diphenyl-4a,5,7,7a-tetrahydro-1H-imidazo[4,5-e]-1,2,4-triazin-6(4H)-ones with 3,5-di-tert-butyl-1,2-benzoquinone 1 and 4,6-di-tert-butyl-3-nitro-1,2-benzoquinone 2, respectively. Photochemical transformations of compounds 9 and 10a as well as products of its photooxygenation involving singlet oxygen under UV irradiation: urea 16, isomeric
    5,7-二叔丁基-1,3-二甲基-3a,9a-二苯基-3,3a-二氢-1 H-苯并[5,6] [1,4]二恶英[2, 3- d ]咪唑-2(9A ħ) -酮13和复杂9的4,6-二-叔丁基-3-硝基苯-1,2-二醇与1,3-二甲基-4,5-二苯基通过3-烷硫基5,7-二甲基-4a,7a-二苯基-4a,5,7,7a-四氢-1 H-咪唑的反应制备1 H-咪唑-2(3 H)-1 10a。 4,5-e] -1,2,4-三嗪-6(4 H)-ones与3,5-二叔丁基-1,2-苯醌1和4,6-二叔丁基-丁基-3-硝基-1,2-苯醌2。化合物的光化学转化9和10a中涉及UV辐射下单线态氧以及其光氧化的产品:尿素16,异构体的1,3-二甲基-4,5- diphenylimidazolidin -2-酮17和17' ,和化合物18进行了研究通过光谱动力学方法。获得了有关合成化合物及其光产物的吸收和荧光性质的数据。
  • Cascade synthesis of the first imidazo[4,5-e]-thiazolo[2,3-c][1,2,4]triazine derivative
    作者:Angelina N. Kravchenko、Galina A. Gazieva、Sergei V. Vasilevskii、Yulia V. Nelyubina
    DOI:10.1016/j.mencom.2014.03.019
    日期:2014.3
    (Z)-7-(3,5-Di-tert-butyl-6-oxocyclohexa-2,4-dien-1-ylidene)-1,3-dimethyl-3a,9a-diphenyl-1,3 a,4,9 a-tetrahydroimidazo[4,5-e]thiazolo[2,3-c][1,2,4]triazine-2,8(3H,7H)-dione was obtained by aldol condensation of 3,5-di-tert-butyl-1,2-benzoquinone with 1,3-dimethyl-3a,9a-diphenyl-3,3a,9,9a-tetrahydroimidazo[4,5-e]thiazolo[3,2-b][1,2,4]triazine-2,7(1H,6H)-dione followed by intramolecular thiazole ring-opening/closing in the condensation primary adduct.
  • Condensation of 5,7-dimethyl-4a,7a-diphenyl-3-thioxoperhydroimidazo[4,5-e]-1,2,4-triazin-6-one with halogenoacetic acids
    作者:Sergei V. Vasilevskii、Pavel A. Belyakov、Galina A. Gazieva、Yulia V. Nelyubina、Natal’ya G. Kolotyrkina、Angelina N. Kravchenko
    DOI:10.1016/j.mencom.2010.01.018
    日期:2010.1
    The reaction of 5,7-dimethyl-4a,7a-diphenyl-3-thioxoperhydroimidazo[4,5-e]-1,2,4-triazin-6-one with halogenoacetic acids was studied, and the directed synthesis of (5,7-dimethyl-6-oxo-4a,7a-diphenyl-4,4a,5,6,7,7a-hexahydro-1H-imidazo[4,5-e]-1,2,4-triazin-3-yl)thio} acetic acid and 1,3-dimethyl-3a,9a-diphenyl-3,3a,9,9a-tetrahydroimidazo[4,5-e]-1,3-thiazolo[3,2-b]-1,2,4-triazine-2,7(1H,6H)-dione was perfomed for the first time; the structures of title compounds were confirmed by the (1)H-(13)C} HMBC, (1)H-(15)N} HSQC, TOCSY, NOESY, HMBC, HSQCED NMR spectroscopy methods and XRD analysis of the tricyclic product.
  • Synthesis of 7-oxindolylidene-3a,9a-diphenylimidazothiazolo[2,3-c][1,2,4]triazines by skeletal rearrangement of their [3,2-b]-fused isomers
    作者:Alexei N. Izmest'ev、Angelina N. Kravchenko、Galina A. Gazieva
    DOI:10.1016/j.mencom.2022.09.037
    日期:2022.9
    Previously unavailable 7-oxindolylidene-1,3-dimethyl-3a,9adiphenylimidazo[4,5-e]thiazolo[2,3-c][1,2,4]triazines were obtained in 63–90% yields by skeletal amidine rearrangement of the thiazolo-triazine system in the corresponding imidazo[4,5-e]thiazolo[3,2-b][1,2,4]triazines on treatment with sodium methoxide.
    以前无法获得的 7-oxindolylidene-1,3-dimethyl-3a,9adiphenylimidazo[4,5- e ]thiazolo[2,3 - c ][1,2,4]triazines 通过骨架脒重排获得 63-90% 的产率用甲醇钠处理相应的咪唑并[4,5 -e ]噻唑并[3,2- b ][1,2,4]三嗪中的噻唑三嗪体系。
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