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3-(4-chloroanilino)-10-(4-chlorophenyl)-2,10-dihydro-2-<(4-piperidinylmethyl)imino>phenazine | 111436-12-5

中文名称
——
中文别名
——
英文名称
3-(4-chloroanilino)-10-(4-chlorophenyl)-2,10-dihydro-2-<(4-piperidinylmethyl)imino>phenazine
英文别名
N,5-bis(4-chlorophenyl)-3-(piperidin-4-ylmethylimino)phenazin-2-amine
3-(4-chloroanilino)-10-(4-chlorophenyl)-2,10-dihydro-2-<(4-piperidinylmethyl)imino>phenazine化学式
CAS
111436-12-5
化学式
C30H27Cl2N5
mdl
——
分子量
528.484
InChiKey
HWPSUHHVDHSIFZ-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):
    6.6
  • 重原子数:
    37
  • 可旋转键数:
    5
  • 环数:
    6.0
  • sp3杂化的碳原子比例:
    0.2
  • 拓扑面积:
    52
  • 氢给体数:
    2
  • 氢受体数:
    5

反应信息

  • 作为产物:
    描述:
    4-氨甲基哌啶 、 氯苯吩嗪环合物盐酸盐 以 1,4-二氧六环 为溶剂, 反应 5.0h, 以70%的产率得到3-(4-chloroanilino)-10-(4-chlorophenyl)-2,10-dihydro-2-<(4-piperidinylmethyl)imino>phenazine
    参考文献:
    名称:
    Clofazimine analogs active against a clofazimine-resistant organism
    摘要:
    Clofazimine analogues active against a strain of Mycobacterium smegmatis 607 made resistant to the antileprosy agent have been synthesized. Activity (i.e., less than or equal to 2 micrograms/mL causing complete inhibition of growth) requires that there be a basic nitrogen in the "rimino" side chain and that the spacer distance between this nitrogen and the imino nitrogen be at least three carbon atoms. The nitrogen may be primary, secondary, or tertiary and may be part of an open chain or enclosed in a ring compound. Provided that the criteria of basicity and spacer distance are satisfied, all are active in vitro against both the sensitive and resistant strains. Substitution elsewhere in the molecule had little effect on the activity. The compounds have been shown to have growth inhibitory activity against human-derived Mycobacterium leprae in murine macrophages in culture.
    DOI:
    10.1021/jm00398a013
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文献信息

  • Clofazimine analogs active against a clofazimine-resistant organism
    作者:John F. O'Sullivan、Michael L. Conalty、Norman E. Morrison
    DOI:10.1021/jm00398a013
    日期:1988.3
    Clofazimine analogues active against a strain of Mycobacterium smegmatis 607 made resistant to the antileprosy agent have been synthesized. Activity (i.e., less than or equal to 2 micrograms/mL causing complete inhibition of growth) requires that there be a basic nitrogen in the "rimino" side chain and that the spacer distance between this nitrogen and the imino nitrogen be at least three carbon atoms. The nitrogen may be primary, secondary, or tertiary and may be part of an open chain or enclosed in a ring compound. Provided that the criteria of basicity and spacer distance are satisfied, all are active in vitro against both the sensitive and resistant strains. Substitution elsewhere in the molecule had little effect on the activity. The compounds have been shown to have growth inhibitory activity against human-derived Mycobacterium leprae in murine macrophages in culture.
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