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1-(1-Undecyl)-2-(4-fluorobenzyl)thio-5-(1-(dimethylaminocarbonylmethyl)-2-oxopyrimid-5-ylmethyl)pyrimidin4-one

中文名称
——
中文别名
——
英文名称
1-(1-Undecyl)-2-(4-fluorobenzyl)thio-5-(1-(dimethylaminocarbonylmethyl)-2-oxopyrimid-5-ylmethyl)pyrimidin4-one
英文别名
2-[5-[[2-[(4-fluorophenyl)methylsulfanyl]-4-oxo-1-undecylpyrimidin-5-yl]methyl]-2-oxopyrimidin-1-yl]-N,N-dimethylacetamide
1-(1-Undecyl)-2-(4-fluorobenzyl)thio-5-(1-(dimethylaminocarbonylmethyl)-2-oxopyrimid-5-ylmethyl)pyrimidin4-one化学式
CAS
——
化学式
C31H42FN5O3S
mdl
——
分子量
583.8
InChiKey
FZQYUWDOZNRTMM-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):
    6.1
  • 重原子数:
    41
  • 可旋转键数:
    17
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.52
  • 拓扑面积:
    111
  • 氢给体数:
    0
  • 氢受体数:
    5

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

反应信息

  • 作为产物:
    描述:
    1-Undecyl-2-(4-fluorobenzyl)thio-5-(1-(carboxymethyl)-2-oxopyrimid-5-ylmethyl)pyrimidin-4-one盐酸二甲胺N,N-二异丙基乙胺4-羟基苯并三唑盐酸-N-乙基-Nˊ-(3-二甲氨基丙基)碳二亚胺 在 SiO2 、 甲醇乙酸乙酯 作用下, 以 二氯甲烷甲醇potassium carbonate 为溶剂, 反应 24.0h, 以to give the desired product (0.085 g)的产率得到1-(1-Undecyl)-2-(4-fluorobenzyl)thio-5-(1-(dimethylaminocarbonylmethyl)-2-oxopyrimid-5-ylmethyl)pyrimidin4-one
    参考文献:
    名称:
    Pyrimidinone derivatives for the treatment of atherosclerosis
    摘要:
    式(I)的嘧啶酮是LpPLA2酶的抑制剂,可用于治疗动脉粥样硬化等疾病,其中:R1是COOH或其盐,COOR10,CONR11R12,CN或CH2OH; R2是单环或双环芳香环系或单环或双环杂芳香环系; R3是C1-20烷基,C3-6环烷基,C3-6环烷基C1-5烷基,C1-10烷氧基C1-10烷基,或芳香环或杂芳香环系; W是SO2或键; X是O或S; Y是式A1-A2-A3的基团,其中A1和A3分别表示键或直链或支链烷基,所述烷基含有1至10个碳原子,并且A2表示键或O、S、SO、SO2、CO、C═CH2、CONH、NHCO、CR15R16、CH═CH或C═C,但当A2是O、S、SO、SO2或CONH时,A3含有至少两个碳原子连接式(I)中的A2基团和CH2基团。
    公开号:
    US06559155B1
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文献信息

  • PYRIMIDINONE DERIVATIVES FOR THE TREATMENT OF ATHEROSCLEROSIS
    申请人:SmithKline Beecham plc
    公开号:EP1105377B1
    公开(公告)日:2003-10-08
  • US6559155B1
    申请人:——
    公开号:US6559155B1
    公开(公告)日:2003-05-06
  • [EN] PYRIMIDINONE DERIVATIVES FOR THE TREATMENT OF ATHEROSCLEROSIS<br/>[FR] DERIVES DE PYRIMIDINONE DESTINES AU TRAITEMENT DE L'ATHEROSCLEROSE
    申请人:SMITHKLINE BEECHAM PLC
    公开号:WO2000010980A1
    公开(公告)日:2000-03-02
    Pyrimidones of formula (I) are inhibitors of the enzyme LpPLA2 and thereof use in treating inter alia atherosclerosis. In formula (I), R1 is COOH or a salt thereof, COOR?10, CONR11R12¿, CN or CH¿2OH; R?2 is a mono- or bicyclic aromatic ring system or a mono- or bicyclic heteroaromatic ring system; R3 is C¿1-20?alkyl, C3-6cycloalkylC3-6cycloalkylC1-5alkyl, C1-10alkoxyC1-10alkyl, or an aromatic or heteroaromatic ring system; W is SO2 or a bond; X is O or S; and Y is a group of the formula A?1-A2-A3¿- in which A?1 and A3¿ each represent a bond or a straight chain or branched alkylene group, said alkylene group(s) containing a total of 1 to 10 carbon atoms and A2 represents a bond or O, S, SO, SO¿2?, CO, C=CH2, CONH, NHCO, CR?15R16¿, CH=CH or C C, providing that when A2 is O, S, SO, SO¿2? or CONH, A?3¿ contains at least two carbon atoms linking the A2 group and the CH¿2? group in formula (I).
  • Pyrimidinone derivatives for the treatment of atherosclerosis
    申请人:SmithKline Beecham p.l.c.
    公开号:US06559155B1
    公开(公告)日:2003-05-06
    Pyrimidones of formula (I) are inhibitors of the enzyme LpPLA2 and thereof use in treating inter alia atherosclerosis, in which: R1 is COOH or a salt thereof, COOR10, CONR11R12, CN or CH2OH; R2 is a mono- or bicyclic aromatic ring system or a mono- or bicyclic heteroaromatic ring system; R3 is C1-20alkyl, C3-6cycloalkyl, C3-6cycloalkylC1-5alkyl, C1-10alkoxyC1-10alkyl, or an aromatic or heteroaromatic ring system; W is SO2 or a bond; X is O or S; and Y is a group of the formula A1—A2—A3 in which A1 and A3 each represent a bond or a straight chain or branched alkylene group, said alkylene group(s) containing a total of 1 to 10 carbon atoms and A2 represents a bond or O, S, SO, SO2, CO, C═CH2, CONH, NHCO, CR15R16, CH═CH or C═C, providing that when A2 is O, S, SO, SO2 or CONH, A3 contains at least two carbon atoms linking the A2 group and the CH2 group in formula (I).
    式(I)的嘧啶酮是LpPLA2酶的抑制剂,可用于治疗动脉粥样硬化等疾病,其中:R1是COOH或其盐,COOR10,CONR11R12,CN或CH2OH; R2是单环或双环芳香环系或单环或双环杂芳香环系; R3是C1-20烷基,C3-6环烷基,C3-6环烷基C1-5烷基,C1-10烷氧基C1-10烷基,或芳香环或杂芳香环系; W是SO2或键; X是O或S; Y是式A1-A2-A3的基团,其中A1和A3分别表示键或直链或支链烷基,所述烷基含有1至10个碳原子,并且A2表示键或O、S、SO、SO2、CO、C═CH2、CONH、NHCO、CR15R16、CH═CH或C═C,但当A2是O、S、SO、SO2或CONH时,A3含有至少两个碳原子连接式(I)中的A2基团和CH2基团。
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