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1-[(1,2,3,4,7,8,9,10-octahydro-8-methyl-2,3-dioxopyrido[4,3-f]quinoxalin-6-yl)sulfonyl)-pyrrolidine | 156695-23-7

中文名称
——
中文别名
——
英文名称
1-[(1,2,3,4,7,8,9,10-octahydro-8-methyl-2,3-dioxopyrido[4,3-f]quinoxalin-6-yl)sulfonyl)-pyrrolidine
英文别名
8-methyl-6-pyrrolidin-1-ylsulfonyl-4,7,9,10-tetrahydro-1H-pyrido[4,3-f]quinoxaline-2,3-dione
1-[(1,2,3,4,7,8,9,10-octahydro-8-methyl-2,3-dioxopyrido[4,3-f]quinoxalin-6-yl)sulfonyl)-pyrrolidine化学式
CAS
156695-23-7
化学式
C16H20N4O4S
mdl
——
分子量
364.425
InChiKey
KISONDNIMLPRGV-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
  • 重原子数:
    25
  • 可旋转键数:
    2
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.5
  • 拓扑面积:
    107
  • 氢给体数:
    2
  • 氢受体数:
    6

文献信息

  • NOVEL QUINOXALINEDIONE DERIVATIVES, THEIR PREPARATION AND USE
    申请人:——
    公开号:US20030114422A1
    公开(公告)日:2003-06-19
    A compound having the formula 1 or a pharmaceutically acceptable salt thereof wherein R is hydrogen or hydroxy; R 1 is hydrogen, alkyl, arylalkyl, (CH 2 ) n OH, or (CH 2 ) NR 7 R 8 ; R 5 and R 6 are each independently hydrogen, halogen, NO 2 , CN, CF 3 , SO 2 NR 7 R 8 , PO 3 R 9 R 10 , alkyl, alkenyl, alkynyl, (CH 2 ) n CONR 7 R 8 , (CH 2 ) n CO 2 R 10 , NHCOR 11 , wherein R 7 and R 8 are each independently hydrogen or alkyl or together R 7 and R 8 form a ring of from three to seven atoms, R 9 is hydrogen or alkyl, R 10 is hydrogen or alkyl, R 11 is hydrogen or alkyl, and n is an integer of from zero to four; A is a ring of five to seven atoms fused with the benzo ring at the positions marked a and b, and formed by the following bivalent radicals: a-NR 12 —CHR 13 —CHR 14 -b, a-CHR 13 —CHR 14 —NR 12 -b, a-CHR 13 —NR 12 —CHR 14 -b, a-CHR 14 —CH 2 —NR 12 —CHR 13 -b, a-CHR 13 —NR 12 —CH 2 —CHR 14 -b, a-CH 2 —CH 2 —CHR 13 —NR 12 -b, a-NR 12 —CHR 12 —CHR 13 —CH 2 —CH 2 -b, a-CH 2 —CH 2 —NR 12 —CH 2 —CH 2 -b, a-CH 2 —CH 2 —CH 2 NR 12 —CH 2 -b, a-CH 2 —NR 12 —CH 2 —CH 2 -b a-CH 2 —CH 2 —CH 2 —CH 2 —NR 12 -b, a-NR 12 —CH 2 —CH 2 —CH 2 —CH 2 -b, wherein R 12 is hydrogen, CH 2 CH 2 OH, or alkyl, and R 13 and R 14 are each independently hydrogen, CN, CONH 2 , CH 2 NH 2 , CH 2 OH, alkyl, arylalkyl, alkenyl, or CO 2 R 15 , wherein R 15 is hydrogen or alkyl. The compounds are useful in the treatment of disorders of mammals, responsive to the blockade of glutamic and aspartic acid receptors. Processes for preparing the compounds and novel intermediate useful in the processes are also included.
    具有以下式1的化合物或其药学上可接受的盐,其中R为氢或羟基;R1为氢、烷基、芳基烷基、(CH2)nOH或( )NR7R8;R5和R6各自独立地为氢、卤素、NO2、CN、CF3、SO2NR7R8、PO3R9R10、烷基、烯基、炔基、( )nCONR7R8、( )nCO2R10、NHCOR11,其中R7和R8各自独立地为氢或烷基,或者一起形成由三至七个原子组成的环的R7和R8;R9为氢或烷基,R10为氢或烷基,R11为氢或烷基,n为从零到四的整数;A为与苯环在标记为a和b的位置融合的五至七个原子组成的环,并由以下二价基团形成:a-NR12—CHR13—CHR14-b,a-CHR13—CHR14—NR12-b,a-CHR13—NR12—CHR14-b,a-CHR14— —NR12—CHR13-b,a-CHR13—NR12— —CHR14-b,a- — —CHR13—NR12-b,a-NR12—CHR12—CHR13— — -b,a- — —NR12— — -b,a- — — NR12— -b,a- —NR12— — -b,a- — — — —NR12-b,a-NR12— — — — -b,其中R12为氢、 OH或烷基,R13和R14各自独立地为氢、CN、CONH2、 NH2、 OH、烷基、芳基烷基、烯基或CO2R15,其中R15为氢或烷基。这些化合物在治疗对谷酸和天冬氨酸受体阻滞有反应的哺乳动物的疾病中有用。还包括用于制备这些化合物的方法和在这些方法中有用的新中间体。
  • QUINOXALINEDIONE DERIVATIVES AS EAA ANTAGONISTS
    申请人:WARNER-LAMBERT COMPANY
    公开号:EP0664807B1
    公开(公告)日:1997-09-10
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