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2-chloro-6a,7-dihydro-5H-dibenzo[b,f]quinolizine-5,12(6H)-dione | 220327-66-2

中文名称
——
中文别名
——
英文名称
2-chloro-6a,7-dihydro-5H-dibenzo[b,f]quinolizine-5,12(6H)-dione
英文别名
2-chloro-6a,7-dihydro-6H-isoquinolino[2,3-a]quinoline-5,12-dione
2-chloro-6a,7-dihydro-5H-dibenzo[b,f]quinolizine-5,12(6H)-dione化学式
CAS
220327-66-2
化学式
C17H12ClNO2
mdl
——
分子量
297.741
InChiKey
PCWJIRGKLCKVAH-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):
    3.2
  • 重原子数:
    21
  • 可旋转键数:
    0
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.18
  • 拓扑面积:
    37.4
  • 氢给体数:
    0
  • 氢受体数:
    2

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

  • 作为反应物:
    描述:
    2-chloro-6a,7-dihydro-5H-dibenzo[b,f]quinolizine-5,12(6H)-dionepotassium carbonatehydroxylamine-O-sulfonic acid 作用下, 生成 2-chloro-6a,7-dihydro-5H-dibenzo[b,f]quinolizine-5,12(6H)-dione 5-oxime-O-sulfonic acid potassium salt
    参考文献:
    名称:
    Synthesis and diuretic activity of 4,5-dihydro-6H-imidazo[4,5,1-ij]quinoline-6-one6-oxime-O-sulfonic acid derivatives
    摘要:
    Using our previously reported 7-chloro-2,3-dihydro-1-(2-methylbenzoyl)-4(1H)-quinolinone 4-oxime-O-sulfonic acid potassium salt 1a (M17055) as a lead, a series of tricyclic (2a-o, 3, 4, 5) and tetracyclic (6) quinolinone oxime O-sulfonic acid derivatives were synthesized by ring annulation of the 1-(2-methylbenzoyl) moiety to the quinolinone skeleton. They were compared with furosemide and compound la for diuretic activity in dogs; some tricyclic 4,5-dihydro-6H-imidazo[4,5,1-ij]quinoline-6-one 6-oxime-O-sulfonic acid derivatives showed diuretic activity comparable (2c,e) or superior (2m) to the lead compound la. These results are discussed on the basis of a comparison of the conformational and electronic characteristics of the relevant compounds with the aid of computer graphics. (C) Elsevier, Paris.
    DOI:
    10.1016/s0223-5234(99)80028-2
  • 作为产物:
    描述:
    2-(3-氯苯基)-4H-异喹啉-1,3-二酮sodium hydroxide 、 sodium tetrahydroborate 、 phosphorus pentoxide 、 sodium hydride 作用下, 以 四氢呋喃甲醇乙醇二氯甲烷甲苯 为溶剂, 反应 3.5h, 生成 2-chloro-6a,7-dihydro-5H-dibenzo[b,f]quinolizine-5,12(6H)-dione
    参考文献:
    名称:
    Synthesis and diuretic activity of 4,5-dihydro-6H-imidazo[4,5,1-ij]quinoline-6-one6-oxime-O-sulfonic acid derivatives
    摘要:
    Using our previously reported 7-chloro-2,3-dihydro-1-(2-methylbenzoyl)-4(1H)-quinolinone 4-oxime-O-sulfonic acid potassium salt 1a (M17055) as a lead, a series of tricyclic (2a-o, 3, 4, 5) and tetracyclic (6) quinolinone oxime O-sulfonic acid derivatives were synthesized by ring annulation of the 1-(2-methylbenzoyl) moiety to the quinolinone skeleton. They were compared with furosemide and compound la for diuretic activity in dogs; some tricyclic 4,5-dihydro-6H-imidazo[4,5,1-ij]quinoline-6-one 6-oxime-O-sulfonic acid derivatives showed diuretic activity comparable (2c,e) or superior (2m) to the lead compound la. These results are discussed on the basis of a comparison of the conformational and electronic characteristics of the relevant compounds with the aid of computer graphics. (C) Elsevier, Paris.
    DOI:
    10.1016/s0223-5234(99)80028-2
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文献信息

  • Synthesis and diuretic activity of 4,5-dihydro-6H-imidazo[4,5,1-ij]quinoline-6-one6-oxime-O-sulfonic acid derivatives
    作者:Kazumi Nishijima、Tomoaki Shinkawa、Manabu Ito、Hidemitsu Nishida、Ichirou Yamamoto、Yoshiaki Onuki、Hitoshi Inaba、Soutarou Miyano
    DOI:10.1016/s0223-5234(99)80028-2
    日期:1998.10
    Using our previously reported 7-chloro-2,3-dihydro-1-(2-methylbenzoyl)-4(1H)-quinolinone 4-oxime-O-sulfonic acid potassium salt 1a (M17055) as a lead, a series of tricyclic (2a-o, 3, 4, 5) and tetracyclic (6) quinolinone oxime O-sulfonic acid derivatives were synthesized by ring annulation of the 1-(2-methylbenzoyl) moiety to the quinolinone skeleton. They were compared with furosemide and compound la for diuretic activity in dogs; some tricyclic 4,5-dihydro-6H-imidazo[4,5,1-ij]quinoline-6-one 6-oxime-O-sulfonic acid derivatives showed diuretic activity comparable (2c,e) or superior (2m) to the lead compound la. These results are discussed on the basis of a comparison of the conformational and electronic characteristics of the relevant compounds with the aid of computer graphics. (C) Elsevier, Paris.
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