2-(Isopropylamino-methyl)-7-nitro-1,2,3,4-tetrahydro-quinoline-6-carbaldehyde; compound with (E)-but-2-enedioic acid | 114719-39-0

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 喹啉及其衍生物
• 英文名称: 2-(Isopropylamino-methyl)-7-nitro-1,2,3,4-tetrahydro-quinoline-6-carbaldehyde; compound with (E)-but-2-enedioic acid
• CAS: 114719-39-0
• 化学式: C₄H₄O₄*2C₁₄H₁₉N₃O₃
• 分子量: 670.72
• InChiKey: XQAZTKYDQNELOC-WLHGVMLRSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.84
• 重原子数：
  28.0
• 可旋转键数：
  7.0
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.39
• 拓扑面积：
  158.87
• 氢给体数：
  4.0
• 氢受体数：
  7.0

反应信息

• 作为反应物：
  描述：

  2-(Isopropylamino-methyl)-7-nitro-1,2,3,4-tetrahydro-quinoline-6-carbaldehyde; compound with (E)-but-2-enedioic acid 在 aq. base 作用下， 以 甲醇 为溶剂， 生成 (6-Diazomethyl-7-nitro-1,2,3,4-tetrahydro-quinolin-2-ylmethyl)-isopropyl-amine
  参考文献：
  名称：

  Studies on some derivatives of oxamniquine

  摘要：

  On the basis of the remarkable biological similarities between hycanthone and oxamniquine and as a sequel to our finding that some esters of hycanthone are active against hycanthone-resistant schistosomes, we prepared oxamniquine acetate, oxamniquine N-methylcarbamate, and four substituted phenylsulfonohydrazones of oxamniquine aldehyde. These compounds were tested for their effect on survival of and on [3H]uridine incorporation into hycanthone-sensitive and -resistant Schistosoma mansoni. All of these derivatives were effective to a greater or lesser degree in killing worms and in inhibiting [3H]uridine incorporation in the sensitive strain, but none was effective in the resistant strain.

  DOI：

  10.1021/jm00403a024