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9-[2-(3-Fluoro-phenyl)-2-hydroxy-ethyl]-2-pyrimidin-4-yl-6,7,8,9-tetrahydro-pyrimido[1,2-a] pyrimidin-4-one | 502927-44-8

中文名称
——
中文别名
——
英文名称
9-[2-(3-Fluoro-phenyl)-2-hydroxy-ethyl]-2-pyrimidin-4-yl-6,7,8,9-tetrahydro-pyrimido[1,2-a] pyrimidin-4-one
英文别名
9-[2-(3-fluorophenyl)-2-hydroxyethyl]-2-pyrimidin-4-yl-7,8-dihydro-6H-pyrimido[1,2-a]pyrimidin-4-one
9-[2-(3-Fluoro-phenyl)-2-hydroxy-ethyl]-2-pyrimidin-4-yl-6,7,8,9-tetrahydro-pyrimido[1,2-a] pyrimidin-4-one化学式
CAS
502927-44-8
化学式
C19H18FN5O2
mdl
——
分子量
367.383
InChiKey
BVWLJFCVRSXPQR-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):
    0.5
  • 重原子数:
    27
  • 可旋转键数:
    4
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.26
  • 拓扑面积:
    81.9
  • 氢给体数:
    1
  • 氢受体数:
    6

文献信息

  • 2-pyrimidinyl-6,7,8,9-tetrahydropyrimido[1,2-a]Pyrimidin-4-one and 7-Pyrimidinyl-2,3-Dihydroimidazo[1,2-a]Pyrimidin-5(1H)one derivatives
    申请人:SANOFI-SYNTHELABO
    公开号:EP1295884A1
    公开(公告)日:2003-03-26
    The invention relates to a pyrimidone derivative represented by formula (I) or a salt thereof: wherein: X represents two hydrogen atoms, a sulphur atom, an oxygen atom or a C1-2 alkyl group and a hydrogen atom; Y represents a bond, a ethenylene group, a ethynylene group, a an oxygen atom, a sulphur atom, a sulfonyl group, a sulfoxide group, a carbonyl group, a nitrogen atom being optionally substituted by a C1-6 alkyl group, a phenyl or a benzyl group; or a methylene group optionally substituted; R1 represents a pyrimidine group;    when Y represents a bond, a methylene group optionally substituted or a carbonyl group then R2 represents a C1-6 alkyl group optionally substituted by a C6,10 aryloxy or a C6,10 arylamino group ; a C 3-6 cycloalkyl group, a C1-4 alkylthio group, a C1-4 alkoxy group, a C1-2 perhalogenated alkyl group, a C1-3 halogenated alkyl group, a phenylthio group, a benzyl group, a phenyl ring, a 5,6,7,8-tetrahydronaphthyl ring, a naphthyl ring, a pyridyl ring, a pyrrole ring, a thiophene ring, a furan ring or an imidazole ring ;    when Y represents a double bond, a triple bond, an oxygen atom, a sulphur atom, a sulfonyl group, a sulfoxyde group or a nitrogen atom being optionally substituted then R2 represents a C1-6 alkyl group (optionally substituted by a C6,10 aryloxy or a C6,10 arylamino group), a C3-6 cycloalkyl group, a C1-2 perhalogenated alkyl group, a C1-3 halogenated alkyl group, a benzyl group, a phenyl ring, a 5,6,7,8-tetrahydronaphthyl ring, a naphthyl ring, a pyridyl ring, a pyrrole ring, a thiophene ring, a furan ring or an imidazole ring ; R3 and R4 represents each independently a hydrogen atom, C1-6 alkyl group, a hydroxy group, a C1-4 alkoxy group or a halogen atom; R5 represents a hydrogen atom, a C1-6 alkyl group or a halogen atom; The invention relates also to a medicament comprising the said derivative or a salt thereof as an active ingredient which is used for preventive and/or therapeutic treatment of a neurodegenerative disease caused by abnormal activity of GSK3β or GSK3β and cdk5/p25, such as Alzheimer disease.
    本发明涉及一种由式(I)表示的嘧啶酮衍生物或其盐: 其中: X代表两个氢原子、硫原子、氧原子或C1-2烷基和一个氢原子; Y代表一个键、一个乙烯基、一个乙炔基、一个氧原子、一个硫原子、一个磺酰基、一个亚磺酸基、一个羰基、一个氮原子,该氮原子可选择地被C1-6烷基、苯基或苄基取代;或一个可选择地取代的亚甲基基团; R1代表一个嘧啶基团; 当Y代表一个键、一个可选择地取代的亚甲基基团或一个羰基时,R2代表一个C1-6烷基,可选择地被C6,10芳氧基或C6,10芳基氨基基团取代;一个C3-6环烷基、一个C1-4烷基硫基、一个C1-4烷氧基、一个C1-2全卤代烷基、一个C1-3卤代烷基、一个苯硫基、一个苄基、一个苯环、一个5,6,7,8-四氢萘环、一个萘环、一个吡啶环、一个吡咯环、一个噻吩环、一个呋喃环或一个咪唑环; 当Y代表一个双键、一个三键、一个氧原子、一个硫原子、一个磺酰基、一个亚磺酸基或一个可选择地取代的氮原子时,R2代表一个C1-6烷基(可选择地被C6,10芳氧基或C6,10芳基氨基基团取代)、一个C3-6环烷基、一个C1-2全卤代烷基、一个C1-3卤代烷基、一个苄基、一个苯环、一个5,6,7,8-四氢萘环、一个萘环、一个吡啶环、一个吡咯环、一个噻吩环、一个呋喃环或一个咪唑环; R3和R4各自独立地代表一个氢原子、C1-6烷基、一个羟基、一个C1-4烷氧基或一个卤原子; R5代表一个氢原子、一个C1-6烷基或一个卤原子; 本发明还涉及一种药物,该药物包括上述衍生物或其盐作为活性成分,用于预防和/或治疗由GSK3β或GSK3β和cdk5/p25的异常活性引起的神经退行性疾病,例如阿尔茨海默病。
  • Substituted 2-pyrimidinyl-6,7,8,9-tetrahydropyrimido[1,2-a]pyrimidin-4-one and 7-pyrimidinyl-2,3-dihydroimidazo[1,2-a]pyrimidin-5(1h)one derivatives for neurodegenerative disorders
    申请人:——
    公开号:US20040266793A1
    公开(公告)日:2004-12-30
    The invention relates to a pyrimidone derivative represented by formula (I) or a salt thereof wherein: X represents two hydrogen atoms, a sulphur atom, an oxygen atom or a C 1-2 alkyl group and a hydrogen atom; y represents a bond, an ethenylene group, an ethynylene group, an oxygen atom, a sulphur atom, a sulfonyl group, a sulfoxide group, a carbonyl group, a nitrogen atom being optionally; or a methylene group optionally substituted; R1 represents a pyrimidine group optionally substituted; R2 may represent a C 1-6 alkyl group optionally substituted by a C 6,10 aryloxy or a C 6,10 arylamino group; a C 3-6 cycloalkyl group, a C 1-4 alkylthio group, a C 1-4 alkoxy group, a C 1-2 perhalogenated alkyl group, a C 1-3 halogenated alkyl group, a phenylthio group, a benzyl group, a benzene ring, an indan ring, a 5,6,7,8-tetrahydronaphthalene ring, a naphthalene ring, a pyridine ring, a pyrrole ring, a thiophene ring, a furan ring or an imidazole ring; R3 and R4 represents each independently a hydrogen atom, C 1-6 alkyl group, a hydroxy group, a C 1- 4 alkoxy group or a halogen atom; R5 represents a hydrogen atom, a C 1-6 alkyl group or a halogen atom. The invention relates also to a medicament comprising the said derivative or a salt thereof as an active ingredient which is used for preventive and/or therapeutic treatment of a neurodegenerative disease caused by abnormal activity of GSK3&bgr;3 or GSK3&bgr;3 and cdk5/p25, such as Alzheimer disease. 1
    本发明涉及一种由式(I)表示的嘧啶酮衍生物或其盐,其中:X代表两个氢原子,硫原子,氧原子或C1-2烷基和氢原子;y代表键,乙烯基,乙炔基,氧原子,硫原子,磺酰基,亚磺酸基,羰基,氮原子(可选)或取代的亚甲基基团;R1表示可选取代的嘧啶基团;R2可以代表C1-6烷基,可选地被C6,10芳氧基或C6,10芳基氨基基团取代;C3-6环烷基,C1-4烷基硫基,C1-4烷氧基,C1-2全氟烷基,C1-3卤代烷基,苯硫基,苄基,苯环,茚环,5,6,7,8-四氢萘环,萘环,吡啶环,吡咯环,噻吩环,呋喃环或咪唑环;R3和R4各自独立地表示氢原子,C1-6烷基,羟基,C1-4烷氧基或卤素原子;R5表示氢原子,C1-6烷基或卤素原子。本发明还涉及一种药物,其中包括所述衍生物或其盐作为活性成分,用于预防和/或治疗由GSK3β3或GSK3β3和cdk5/p25的异常活性引起的神经退行性疾病,例如阿尔茨海默病。
  • Use of Substituted 2-Pyrimidinyl-6,7,8,9-tetrahydropyrimido[1,2-A] Pyrimidin-4-one and 7-Pyrimidinyl-2,3-dihydroimidazo[1,2-A] Pyrimidin-5(1H)one Derivatives
    申请人:Gallet Thierry
    公开号:US20080269257A1
    公开(公告)日:2008-10-30
    The invention relates to use of a pyrimidone derivative represented by formula (I) or a salt thereof as therapeutic agents: Wherein m, n, p, X, Y, R1, R2, R3, R4 R5, are as defined herein. The invention specifically relates to a medicament comprising the said derivative or a salt thereof as an active ingredient which is used for preventive and/or therapeutic treatment of a neurodegenerative disease caused by abnormal activity of GSK3β or GSK3β and cdk5/p25, such as Alzheimer disease.
    该发明涉及使用式(I)所表示的嘧啶酮衍生物或其盐作为治疗剂:其中m、n、p、X、Y、R1、R2、R3、R4、R5如本文中所定义。该发明特别涉及一种药物,包括所述衍生物或其盐作为活性成分,用于预防和/或治疗由GSK3β或GSK3β和cdk5/p25异常活性引起的神经退行性疾病,例如阿尔茨海默病。
  • Substituted 2-pyrimidinyl-6,7,8,9-tetrahydropyrimido[1,2-a]pyrimidin-4-one and 7-pyrimidinyl-2,3-dihydroimidazo[1,2-a]pyrimidin-5(1H)one derivatives
    申请人:SANOFI-SYNTHELABO
    公开号:EP1340760A1
    公开(公告)日:2003-09-03
    The invention relates to a pyrimidone derivative represented by formula (I) or a salt thereof: wherein: X represents two hydrogen atoms, a sulphur atom, an oxygen atom or a C1-2 alkyl group and a hydrogen atom; Y represents a bond, a ethenylene group, a ethynylene group, an oxygen atom, a sulphur atom, a sulfonyl group, a sulfoxide group, a carbonyl group, a nitrogen atom being optionally; or a methylene group optionally substituted; R1 represents a pyrimidine group optionally substituted; R2 may represent a C1-6 alkyl group optionally substituted by a C6,10 aryloxy or a C6,10 arylamino group ; a C3-6 cycloalkyl group, a C1-4alkylthio group, a C1-4alkoxy group, a C1-2 perhalogenated alkyl group, a C1-3 halogenated alkyl group, a phenylthio group, a benzyl group, a phenyl ring, an indanyl ring, a 5,6,7,8-tetrahydronaphthyl ring, a naphthyl ring, a pyridine ring, a pyrrole ring, a thiophene ring, a furan ring or an imidazole ring ; R3 and R4 represents each independently a hydrogen atom, C1-6 alkyl group, a hydroxy group, a C1-4alkoxy group or a halogen atom; R5 represents a hydrogen atom, a C1-6 alkyl group or a halogen atom; The invention relates also to a medicament comprising the said derivative or a salt thereof as an active ingredient which is used for preventive and/or therapeutic treatment of a neurodegenerative disease caused by abnormal activity of GSK3β or GSK3β and cdk5/p25, such as Alzheimer disease.
    本发明涉及式 (I) 所代表的嘧啶酮衍生物或其盐: 其中 X 代表两个氢原子、一个硫原子、一个氧原子或一个 C1-2 烷基和一个氢原子; Y 代表一个键、一个乙烯基、一个乙炔基、一个氧原子、一个硫原子、一个磺酰基、一个亚砜基、一个羰基、一个任选被取代的氮原子或一个任选被取代的亚甲基; R1 代表任选被取代的嘧啶基团; R2 可代表被 C6,10 芳氧基或 C6,10 芳酰胺基任选取代的 C1-6 烷基;C3-6环烷基、C1-4烷硫基、C1-4烷氧基、C1-2过卤代烷基、C1-3卤代烷基、苯硫基、苄基、苯基环、茚基环、5,6,7,8-四氢萘环、萘基环、吡啶环、吡咯环、噻吩环、呋喃环或咪唑环; R3 和 R4 各自独立地代表氢原子、C1-6 烷基、羟基、C1-4 烷氧基或卤素原子; R5 代表氢原子、C1-6 烷基或卤原子; 本发明还涉及一种包含上述衍生物或其盐作为活性成分的药物,该药物用于预防和/或治疗由 GSK3β 或 GSK3β 和 cdk5/p25 活性异常引起的神经退行性疾病,如阿尔茨海默病。
  • SUBSTITUTED 2-PYRIMIDINYL-6,7,8,9-TETRAHYDROPYRIMIDO[1,2-A]PYRIMIDIN-4-ONE AND 7-PYRIMIDINYL-2,3-DIHYDROIMIDAZO[1,2-A]PYRIMIDIN-5(1H)ONE DERIVATIVES FOR NEURODEGENERATIVE DISORDERS
    申请人:Sanofi-Aventis
    公开号:EP1430056B1
    公开(公告)日:2005-10-26
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同类化合物

(N-(2-甲基丙-2-烯-1-基)乙烷-1,2-二胺) (4-(苄氧基)-2-(哌啶-1-基)吡啶咪丁-5-基)硼酸 (11-巯基十一烷基)-,,-三甲基溴化铵 鼠立死 鹿花菌素 鲸蜡醇硫酸酯DEA盐 鲸蜡硬脂基二甲基氯化铵 鲸蜡基胺氢氟酸盐 鲸蜡基二甲胺盐酸盐 高苯丙氨醇 高箱鲀毒素 高氯酸5-(二甲氨基)-1-({(E)-[4-(二甲氨基)苯基]甲亚基}氨基)-2-甲基吡啶正离子 高氯酸2-氯-1-({(E)-[4-(二甲氨基)苯基]甲亚基}氨基)-6-甲基吡啶正离子 高氯酸2-(丙烯酰基氧基)-N,N,N-三甲基乙铵 马诺地尔 马来酸氢十八烷酯 马来酸噻吗洛尔EP杂质C 马来酸噻吗洛尔 马来酸倍他司汀 顺式环己烷-1,3-二胺盐酸盐 顺式氯化锆二乙腈 顺式吡咯烷-3,4-二醇盐酸盐 顺式双(3-甲氧基丙腈)二氯铂(II) 顺式3,4-二氟吡咯烷盐酸盐 顺式1-甲基环丙烷1,2-二腈 顺式-二氯-反式-二乙酸-氨-环己胺合铂 顺式-二抗坏血酸(外消旋-1,2-二氨基环己烷)铂(II)水合物 顺式-N,2-二甲基环己胺 顺式-4-甲氧基-环己胺盐酸盐 顺式-4-环己烯-1.2-二胺 顺式-4-氨基-2,2,2-三氟乙酸环己酯 顺式-2-甲基环己胺 顺式-2-(苯基氨基)环己醇 顺式-2-(氨基甲基)-1-苯基环丙烷羧酸盐酸盐 顺式-1,3-二氨基环戊烷 顺式-1,2-环戊烷二胺 顺式-1,2-环丁腈 顺式-1,2-双氨甲基环己烷 顺式--N,N'-二甲基-1,2-环己二胺 顺式-(R,S)-1,2-二氨基环己烷铂硫酸盐 顺式-(2-氨基-环戊基)-甲醇 顺-2-戊烯腈 顺-1,3-环己烷二胺 顺-1,3-双(氨甲基)环己烷 顺,顺-丙二腈 非那唑啉 靛酚钠盐 靛酚 霜霉威盐酸盐 霜脲氰