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2-Methyl-4,6-diamino-thiazolo<5,4-d>pyrimidin | 89712-91-4

中文名称
——
中文别名
——
英文名称
2-Methyl-4,6-diamino-thiazolo<5,4-d>pyrimidin
英文别名
2-methyl-thiazolo[5,4-d]pyrimidine-5,7-diamine;2-methyl-thiazolo[5,4-d]pyrimidine-5,7-diyldiamine;2-Methyl-thiazolo[5,4-d]pyrimidin-5,7-diyldiamin;2-Methyl-[1,3]thiazolo[5,4-d]pyrimidine-5,7-diamine;2-methyl-[1,3]thiazolo[5,4-d]pyrimidine-5,7-diamine
2-Methyl-4,6-diamino-thiazolo<5,4-d>pyrimidin化学式
CAS
89712-91-4
化学式
C6H7N5S
mdl
——
分子量
181.221
InChiKey
UIVCWPPLMUDDQK-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):
    0.7
  • 重原子数:
    12
  • 可旋转键数:
    0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.17
  • 拓扑面积:
    119
  • 氢给体数:
    2
  • 氢受体数:
    6

反应信息

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文献信息

  • The Direct Thiation of Pyrimidinol Derivatives.
    作者:Takeo Ueda、Tadakazu Tsuji、Hiroko Momona
    DOI:10.1248/cpb.11.912
    日期:——
    The replacement of 4-hydroxyl group of aminopyrimidinols by sulfhydryl in one step, through the action of phosphorus pentasulfide in triethylamine or 3-picoline. 5-Acylamino-6-amino-4-pyrimidinols were treated with phosphorus pentasulfide in pyridine, to yield thiazolo [5, 4-d] pyrimidine and 6-purinethiol compounds. The yield of both two type compounds were changed according to a functional group in the starting substance. These products, in addition, other 6-purinethiol and related compounds were screened as to their antiviral activities on poliomyelitis virus. Any of the compounds, however, did not exert a significant activity on the virus.
    通过三乙胺或3-吡啶的作用,采用五硫化磷在一步中替换氨基嘧啶醇的4-羟基为巯基。5-酰氨基-6-氨基-4-嘧啶醇在吡啶中与五硫化磷反应,得到噻唑并[5, 4-d]嘧啶和6-嘌呤巯基化合物。两种类型化合物的产率根据起始物质中的功能团有所变化。此外,这些产品以及其他6-嘌呤巯基及相关化合物被筛选以评估其对脊髓灰质炎病毒的抗病毒活性。然而,任何化合物都没有对病毒展现出显著的活性。
  • Studies on Condensed Pyrimidine Systems. IV.<sup>1</sup> Some Thiazolo [5,4-d] pyrimidines
    作者:Elvira A. Falco、George H. Hitchings
    DOI:10.1021/ja01163a112
    日期:1950.7
  • Thiazolopyrimidines
    作者:Scott J. Childress、R. L. McKee
    DOI:10.1021/ja01152a090
    日期:1951.8
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同类化合物

噻唑并[5,4-d]嘧啶-7(4H)-酮 噻唑并[5,4-d]嘧啶-5,7(4H,6H)-二酮 噻唑并[5,4-d]嘧啶-2(1H)-酮 噻唑并[5,4-d]嘧啶,5-氯- 噻唑[5,4-D]嘧啶-2-胺 叔丁基-(7-氯噻唑并[5,4-d]嘧啶-2-基)-胺 [1,3]噻唑并[5,4-D]嘧啶-7-胺 N7-丁基-n2-苯基噻唑并[5,4-d]嘧啶-2,7-二胺 N7-(4-甲氧基苯基)-n2-苯基噻唑并[5,4-d]嘧啶-2,7-二胺 N7-(3-氯苯基)-n2-苯基噻唑并[5,4-d]嘧啶-2,7-二胺 N2-苯基-n7-(3,4,5-三甲氧基苄基)噻唑并[5,4-d]嘧啶-2,7-二胺 N2,N7-二苯基-噻唑并[5,4-d]嘧啶-2,7-二胺 N-(7-氯-2-甲基噻唑并[5,4-D]嘧啶-5-基)新戊酰胺 7-氯噻唑并[5,4-D]嘧啶 7-氯-N-(邻甲苯基)噻唑并[5,4-D]嘧啶-2-胺 7-氯-5-甲基-[1,3]噻唑并[5,4-d]嘧啶 7-氯-5-(三氟甲基)[1,3]噻唑并[5,4-d]嘧啶 7-氨基-噻唑并[5,4-d]嘧啶-2(1H)-硫酮 7-(甲硫基)噻唑并[5,4-D]嘧啶-2-羧酸甲酯 5-甲硫基-9-硫杂-2,4,7-三氮杂双环[4.3.0]壬-2,4,7,10-四烯 5,7-二氯噻唑并[5,4-D]嘧啶 5,7-二氯-2-甲基-噻唑并[5,4-d]嘧啶 4-(5-氯噻唑并[5,4-D]嘧啶-7-基)吗啉 2-苯胺基[1,3]噻唑并[5,4-d]嘧啶-7-醇 2-苯基噻唑并[5,4-d]嘧啶-7-胺 2-甲基-4H-噻唑并[5,4-d]嘧啶-5,7-二酮 2-(甲基硫代)-噻唑并[5,4-d]嘧啶-7(4H)-酮 2,7-二氯噻唑并[5,4-D]嘧啶 2,5-二氯噻唑并[5,4-d]嘧啶 2,5-二氨基-6H-[1,3]噻唑并[4,5-e]嘧啶-7-酮 1-(7-氯噻唑并[5,4-d]嘧啶-2-基)-1,3-二甲基硫脲 1,3-二苄基-1-(7-氯噻唑并[5,4-d]嘧啶-2-基)硫脲 (7-氯噻唑并[5,4-d]嘧啶-2-基)苯胺 (7-氯噻唑并[5,4-d]嘧啶-2-基)异丙胺 (7-氯噻唑并[5,4-d]嘧啶-2-基)-对甲苯-胺 (7-氯噻唑并[5,4-d]嘧啶-2-基)-吡啶-3-基-胺 (7-氯噻唑并[5,4-d]嘧啶-2-基)-(4-甲氧基苯基)胺 (7-氯噻唑并[5,4-d]嘧啶-2-基)-(2,6-二甲基苯基)胺 (6CI,7CI,8CI,9CI)-噻唑并[5,4-d]嘧啶 ethyl 5-chlorothiazolo[5,4-d]pyrimidin-2-ylcarbamate N5-(3-fluorobenzyl)-2-(2-furanyl)[1,3]thiazolo[5,4-d]pyrimidine-5,7-diamine 2-methyl-N5-(thiophen-2ylmethyl)thiazolo[5,4-d]pyrimidine-5,7-diamine 2-(pyrazin-2-yl)-N5-(thiophen-2-ylmethyl)thiazolo[5,4-d]pyrimidine-5,7-diamine 2-(thiophen-2-yl)-N5-(thiophen-2-yl-methyl)[1,3]thiazolo[5,4-d]pyrimidine-5,7-diamine 2-phenyl-N5-(thiophen-2-ylmethyl)thiazolo[5,4-d]pyrimidine-5,7-diamine 2-(5-methylfuran-2-yl)-N5-(thiophen-2-yl-methyl)[1,3]thiazolo[5,4-d]pyrimidine-5,7-diamine 2-(furan-2-yl)-N5-(thiophen-2-yl-methyl)[1,3]thiazolo[5,4-d]pyrimidine-5,7-diamine (R)-N-benzyl-2-(5-ethyl-6-methyl-7-oxo-6,7-dihydro[1,3]thiazolo[5,4-d]pyrimidin-2-yl)pyrrolidine-1-carboxamide 2-(4-chlorophenylamino)-7-chlorothiazolo[5,4-d]pyrimidine 5-chlorothiazolo[5,4-d]pyrimidin-2-amine