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2-Thio-4-hydroxy-6-fluormethyl-pyrimidin | 1598-62-5

中文名称
——
中文别名
——
英文名称
2-Thio-4-hydroxy-6-fluormethyl-pyrimidin
英文别名
6-fluoromethyl-2-thioxo-2,3-dihydro-1H-pyrimidin-4-one;6-(fluoromethyl)-2-sulfanylidene-1H-pyrimidin-4-one
2-Thio-4-hydroxy-6-fluormethyl-pyrimidin化学式
CAS
1598-62-5
化学式
C5H5FN2OS
mdl
——
分子量
160.172
InChiKey
PTFKKKOYWVQBCY-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):
    -0.2
  • 重原子数:
    10
  • 可旋转键数:
    1
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.2
  • 拓扑面积:
    73.2
  • 氢给体数:
    2
  • 氢受体数:
    3

反应信息

  • 作为反应物:
    描述:
    2-Thio-4-hydroxy-6-fluormethyl-pyrimidinN-碘代丁二酰亚胺potassium carbonate 作用下, 以 乙腈 为溶剂, 反应 2.5h, 生成 4-(fluoromethyl)-5-iodo-2-methylsulfanyl-1H-pyrimidin-6-one
    参考文献:
    名称:
    [EN] SUBSTITUTED PYRIDINE AND PYRIMIDINE DERIVATIVES AND THEIR USE IN TREATING VIRAL INFECTIONS
    [FR] DÉRIVÉS DE PYRIDINE ET PYRIMIDINE SUBSTITUÉES ET LEUR UTILISATION DANS LE TRAITEMENT D'INFECTIONS VIRALES
    摘要:
    本发明提供了式(I)的化合物:以及所述化合物的互变异构体、同分异构体和酯,以及所述化合物的药学上可接受的盐、溶剂化合物和前药,其中R、R1、X、Y、Z、R2、R3、R4、R5、R6、R7、R8、R9、R18、R19和n中的每个均独立选择并如本文所定义。还提供了包含这些化合物的组合物。本发明的化合物作为HCV的抑制剂是有效的,并且在治疗或预防病毒感染和与病毒相关的疾病或紊乱方面,单独或与其他治疗剂一起使用是有用的。
    公开号:
    WO2010022121A1
  • 作为产物:
    描述:
    4-氟-3-氧代丁酸乙酯硫脲sodium methylate 作用下, 以 甲醇 为溶剂, 反应 48.0h, 以1.26 g的产率得到2-Thio-4-hydroxy-6-fluormethyl-pyrimidin
    参考文献:
    名称:
    Substituted pyridine and pyrimidine derivatives and their use in treating viral infections
    摘要:
    本发明提供了式(I)的化合物:以及所述化合物的互变异构体、异构体和酯,以及所述化合物的药学上可接受的盐、溶剂化合物和前药,其中R、R1、X、Y、Z、R2、R3、R4、R5、R6、R7、R8、R9、R18、R19和n中的每个都是独立选择并如本文所定义。还提供了包含这些化合物的组合物。本发明的化合物作为HCV的抑制剂是有效的,并且在治疗或预防病毒感染和与病毒相关的疾病或紊乱方面,单独或与其他治疗剂一起使用是有用的。
    公开号:
    US09433621B2
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文献信息

  • [EN] SUBSTITUTED PYRIDINE AND PYRIMIDINE DERIVATIVES AND THEIR USE IN TREATING VIRAL INFECTIONS<br/>[FR] DÉRIVÉS DE PYRIDINE ET PYRIMIDINE SUBSTITUÉES ET LEUR UTILISATION DANS LE TRAITEMENT D'INFECTIONS VIRALES
    申请人:SCHERING CORP
    公开号:WO2010022121A1
    公开(公告)日:2010-02-25
    The present invention provides compounds of Formula (I): and tautomers, isomers, and esters of said compounds, and pharmaceutically acceptable salts, solvates, and prodrugs of said compounds, wherein wherein each of R, R1, X, Y, Z, R2, R3, R4, R5, R6, R7, R8, R9, R18, R19 and n is selected independently and as defined herein. Compositions comprising such compounds are also provided. The compounds of the invention are effective as inhibitors of HCV, and are useful, alone and together with other therapeutic agents, in treating or preventing diseases or disorders such as viral infections and virus-related disorders.
    本发明提供了式(I)的化合物:以及所述化合物的互变异构体、同分异构体和酯,以及所述化合物的药学上可接受的盐、溶剂化合物和前药,其中R、R1、X、Y、Z、R2、R3、R4、R5、R6、R7、R8、R9、R18、R19和n中的每个均独立选择并如本文所定义。还提供了包含这些化合物的组合物。本发明的化合物作为HCV的抑制剂是有效的,并且在治疗或预防病毒感染和与病毒相关的疾病或紊乱方面,单独或与其他治疗剂一起使用是有用的。
  • Substituted pyridine and pyrimidine derivatives and their use in treating viral infections
    申请人:Arasappan Ashok
    公开号:US09433621B2
    公开(公告)日:2016-09-06
    The present invention provides compounds of Formula (I): and tautomers, isomers, and esters of said compounds, and pharmaceutically acceptable salts, solvates, and prodrugs of said compounds, wherein each of R, R1, X, Y, Z, R2, R3, R4, R5, R6, R7, R8, R9, R18, R19 and n is selected independently and as defined herein. Compositions comprising such compounds are also provided. The compounds of the invention are effective as inhibitors of HCV, and are useful, alone and together with other therapeutic agents, in treating or preventing diseases or disorders such as viral infections and virus-related disorders.
    本发明提供了式(I)的化合物:以及所述化合物的互变异构体、异构体和酯,以及所述化合物的药学上可接受的盐、溶剂化合物和前药,其中R、R1、X、Y、Z、R2、R3、R4、R5、R6、R7、R8、R9、R18、R19和n中的每个都是独立选择并如本文所定义。还提供了包含这些化合物的组合物。本发明的化合物作为HCV的抑制剂是有效的,并且在治疗或预防病毒感染和与病毒相关的疾病或紊乱方面,单独或与其他治疗剂一起使用是有用的。
  • Source regions and timescales for the delivery of water to the Earth
    作者:A. Morbidelli、J. Chambers、J. I. Lunine、J. M. Petit、F. Robert、G. B. Valsecchi、K. E. Cyr
    DOI:10.1111/j.1945-5100.2000.tb01518.x
    日期:2000.11
    Abstract—In the primordial solar system, the most plausible sources of the water accreted by the Earth were in the outer asteroid belt, in the giant planet regions, and in the Kuiper Belt. We investigate the implications on the origin of Earth's water of dynamical models of primordial evolution of solar system bodies and check them with respect to chemical constraints. We find that it is plausible that the Earth accreted water all along its formation, from the early phases when the solar nebula was still present to the late stages of gas‐free sweepup of scattered planetesimals. Asteroids and the comets from the Jupiter‐Saturn region were the first water deliverers, when the Earth was less than half its present mass. The bulk of the water presently on Earth was carried by a few planetary embryos, originally formed in the outer asteroid belt and accreted by the Earth at the final stage of its formation. Finally, a late veneer, accounting for at most 10% of the present water mass, occurred due to comets from the Uranus‐Neptune region and from the Kuiper Belt. The net result of accretion from these several reservoirs is that the water on Earth had essentially the D/H ratio typical of the water condensed in the outer asteroid belt. This is in agreement with the observation that the D/H ratio in the oceans is very close to the mean value of the D/H ratio of the water inclusions in carbonaceous chondrites.
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