2-(3-(1-butenyl))-4-nitro-6-methoxyphenol | 153001-64-0

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: 2-(3-(1-butenyl))-4-nitro-6-methoxyphenol
• 英文别名: 2-But-3-en-2-yl-6-methoxy-4-nitrophenol
• CAS: 153001-64-0
• 化学式: C₁₁H₁₃NO₄
• 分子量: 223.229
• InChiKey: MGQXUQPJHWFTAE-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.8
• 重原子数：
  16
• 可旋转键数：
  3
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.27
• 拓扑面积：
  75.3
• 氢给体数：
  1
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  2-(3-(1-butenyl))-4-nitro-6-methoxyphenol 在 platinum(IV) oxide 四氯化碳 、 sodium hydroxide 、 palladium on activated charcoal 、 N-溴代丁二酰亚胺(NBS) 、 PPA 、 二甲基硫 、 偶氮二异丁腈 、 硫酸 、 氢气 、 双氧水 、 三正丁基氢锡 、 甲酸铵 、 吡啶盐酸盐 、 sodium hydride 、 臭氧 、 三苯基膦 、 (-)-Monoisopinocampheylborane 作用下， 以 四氢呋喃 、 1,4-二氧六环 、 二氯甲烷 、 乙酸乙酯 、 N,N-二甲基甲酰胺 、 甲苯 、 苯 为溶剂， -78.0~170.0 ℃ 、137.9 kPa 条件下， 反应 32.41h， 生成 (+)-(1R)-1,2-dihydro-1-(chloromethyl)-3-(tert-butyloxycarbonyl)-5-hydroxy-8-methyl-3H-furano<3,2-e>indole
  参考文献：
  名称：

  Total synthesis and biological properties of novel antineoplastic (chloromethyl)furanoindolines: an asymmetric hydroboration mediated synthesis of the alkylation subunits

  摘要：

  1,2-Dihydro-1-(chloromethyl)-5-hydroxy-8-methyl-3H-furano[3,2-e] indole (CFI) as a novel re; placement of the cyclopropylpyrroloindoline (CPI) alkylation subunit of CC-1065, U-71184, and U-73975 (adozelesin) has been synthesized and incorporated into a series of efficacious antineopIastic agents. A partial solution to an asymmetric synthesis of the CFI alkylation subunit has been achieved by the implementation of an asymmetric hydroboration reaction of an intermediate 3-methyleneindoline (13). Extension to the asymmetric synthesis of the CBI and CI alkylation subunits is presented. The demonstration and comparative study of the sequence-selective DNA alkylation properties of the CFI-based agents are detailed, and the preliminary in vitro and in vivo antineoplastic propertes of these agents in the human epidermoid cell lung carcinoma (T222) are described.

  DOI：

  10.1021/jm00028a005
• 作为产物：
  描述：

  potassium 2-methoxy-4-nitrophenolate 在 potassium iodide 作用下， 以 水 、 丙酮 、 甲苯 为溶剂， 反应 32.0h， 生成 2-(3-(1-butenyl))-4-nitro-6-methoxyphenol
  参考文献：
  名称：

  Total synthesis and biological properties of novel antineoplastic (chloromethyl)furanoindolines: an asymmetric hydroboration mediated synthesis of the alkylation subunits

  摘要：

  1,2-Dihydro-1-(chloromethyl)-5-hydroxy-8-methyl-3H-furano[3,2-e] indole (CFI) as a novel re; placement of the cyclopropylpyrroloindoline (CPI) alkylation subunit of CC-1065, U-71184, and U-73975 (adozelesin) has been synthesized and incorporated into a series of efficacious antineopIastic agents. A partial solution to an asymmetric synthesis of the CFI alkylation subunit has been achieved by the implementation of an asymmetric hydroboration reaction of an intermediate 3-methyleneindoline (13). Extension to the asymmetric synthesis of the CBI and CI alkylation subunits is presented. The demonstration and comparative study of the sequence-selective DNA alkylation properties of the CFI-based agents are detailed, and the preliminary in vitro and in vivo antineoplastic propertes of these agents in the human epidermoid cell lung carcinoma (T222) are described.

  DOI：

  10.1021/jm00028a005

文献信息

• Furanoindoline derivatives and their use as antitumor agents
  申请人：ELI LILLY AND COMPANY

  公开号：EP0586254A1

  公开（公告）日：1994-03-09

  This invention provides novel furanoindoline compounds of formula I effective in inhibiting the growth of solid tumors.

  本发明提供了有效抑制实体瘤生长的新型式 I 呋喃吲哚啉化合物。
• US5248691A
  申请人：——

  公开号：US5248691A

  公开（公告）日：1993-09-28