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N-benzylsecoboldine | 144919-04-0

中文名称
——
中文别名
——
英文名称
N-benzylsecoboldine
英文别名
8-[2-[benzyl(methyl)amino]ethyl]-3,5-dimethoxyphenanthrene-2,6-diol
N-benzylsecoboldine化学式
CAS
144919-04-0
化学式
C26H27NO4
mdl
——
分子量
417.505
InChiKey
KQKMGQCCMOXEFO-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):
    5.4
  • 重原子数:
    31
  • 可旋转键数:
    7
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.23
  • 拓扑面积:
    62.2
  • 氢给体数:
    2
  • 氢受体数:
    5

上下游信息

  • 下游产品
    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:
    N-benzylsecoboldine 在 palladium on activated charcoal 氢气 作用下, 以 甲醇溶剂黄146 为溶剂, 生成 9,11-二甲氧基-2-甲基-3,4-二氢-1H-萘并[6,5-f]异喹啉-8,12-二醇
    参考文献:
    名称:
    通过生物遗传学方法从黄嘌呤中轻松合成半胱氨酸,一种新型的菲生物碱
    摘要:
    通过生物遗传学方法从胆碱中半合成立巴明。主要反应包括冯·布劳恩反应,一锅中彻底的苄基化和霍夫曼降解,以及曼尼希反应。
    DOI:
    10.1016/s0040-4039(00)60960-7
  • 作为产物:
    描述:
    氯化苄boldineN,N-二甲基甲酰胺 为溶剂, 反应 2.0h, 以74%的产率得到N-benzylsecoboldine
    参考文献:
    名称:
    通过生物遗传学方法从黄嘌呤中轻松合成半胱氨酸,一种新型的菲生物碱
    摘要:
    通过生物遗传学方法从胆碱中半合成立巴明。主要反应包括冯·布劳恩反应,一锅中彻底的苄基化和霍夫曼降解,以及曼尼希反应。
    DOI:
    10.1016/s0040-4039(00)60960-7
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文献信息

  • Secoaporphine compound on arrhythmia
    申请人:National Science Council
    公开号:US05594033A1
    公开(公告)日:1997-01-14
    Novel secoaporphine compounds having the formula I ##STR1## wherein a) R.sub.1, R.sub.2 and R.sub.3, R.sub.4 are each methyl group; or b) R.sub.1, R.sub.2, and R.sub.4 are each methyl group; R.sub.3 is benzyl, ethyl or allyl; or c) R.sub.1, R.sub.2, and R.sub.3 are each hydrogen, R.sub.4 is methyl; or d) R.sub.1 and R.sub.2 are each hydrogen, R.sub.3 is benzyl, R.sub.4 is methyl; or e) R.sub.1 and R.sub.2 are each hydrogen, R.sub.3 is cyano, R.sub.4 is methyl group, and a salt thereof with a pharmaceutically acceptable acid. The novel compounds are useful in the treatment of arrhythmia.
    具有以下结构式I的新型咔啉类化合物:##STR1## 其中a)R.sub.1、R.sub.2和R.sub.3、R.sub.4均为甲基基团;或b)R.sub.1、R.sub.2和R.sub.4均为甲基基团;R.sub.3为苄基、乙基或丙烯基;或c)R.sub.1、R.sub.2和R.sub.3均为氢,R.sub.4为甲基;或d)R.sub.1和R.sub.2均为氢,R.sub.3为苄基,R.sub.4为甲基;或e)R.sub.1和R.sub.2均为氢,R.sub.3为氰基,R.sub.4为甲基基团,并且其与药学上可接受的酸的盐在心律失常治疗中有用。
  • A facile semisynthesis of litebamine, a novel phenanthrene alkaloid, from boldine via a biogenetical approach
    作者:Lee Shoei-Sheng、Lin Yi-Jen、Chen Mei-Zu、Wu Yang-Chang、Chen Chung-Hsiung
    DOI:10.1016/s0040-4039(00)60960-7
    日期:1992.10
    Litebamine was semisynthesized from boldine via a biogenetical approach. Main reactions include Von Braun reaction, exhaustive benzylation and Hofmann degradation in one pot, and the Mannich reaction.
    通过生物遗传学方法从胆碱中半合成立巴明。主要反应包括冯·布劳恩反应,一锅中彻底的苄基化和霍夫曼降解,以及曼尼希反应。
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同类化合物

防己菲碱 绿唐松草酮 N-去甲基芒籽宁 N,N-二甲基-2-芘-1-基乙胺 ATM44-乙酰氧基类似物 3,4-二甲氧基-N,N-二甲基-1-菲乙胺 trimethyl-(2-oxo-2-pyrene-1-yl-ethyl)-ammonium bromide dimethyl-(2-[1]phenanthryl-ethyl)-amine secocrebanine N-allylsecoboldine 4-Phenanthrenol, 1-(2-(dimethylamino)ethyl)-3,5,6-trimethoxy- 1-(2-Dimethylaminoethyl)-3,6,7-trimethoxyphenanthren-4-ol [2-(5,6-Dihydroxy-phenanthren-1-yl)-ethyl]-methyl-cyanamide 8-[2-[ethyl(methyl)amino]ethyl]-9,10-dihydrophenanthrene-3,4-diol;hydron;bromide 3,4-Phenanthrenediol, 8-(2-(ethylmethylamino)ethyl)-, hydrobromide Acetic acid 5-[2-(cyano-methyl-amino)-ethyl]-10-methoxy-phenanthro[3,4-d][1,3]dioxol-11-yl ester 3,4,5,6-Tetramethoxy-1-(dimethylamino-ethyl)-phenanthren 8-(2-Dimethylamino-ethyl)-phenanthrene-3,4-diol 3,4-Phenanthrenediol, 8-(2-(dimethylamino)ethyl)-, hydrobromide 2.3.5.6-Tetramethoxy-8-<2-dimethylamino-aethyl>-phenanthren-methojodid Dicentrin-methin II N-[2-(9-methoxynaphtho[2,1-g][1,3]benzodioxol-5-yl)ethyl]-N-methylhydroxylamine 1-<2-ethyl>-3,4,6,7-tetramethoxyphenantrene N-carbethoxy-N-methyl-2-(3',4'-dimethoxy-1'-phenanthryl)ethylamine N-benzylsecoboldine [2-(10,11-dimethoxy-phenanthro[3,4-d][1,3]dioxol-5-yl)-ethyl]-dimethyl-amine secoroemerine N-carbethoxysecoglaucine Ethyl-methyl-(2-naphtho[2,1-g][1,3]benzodioxol-5-ylethyl)azanium N-benzyl-2-(3,7-dibutoxy-4,6-dimethoxyphenanthren-1-yl)-N-methylethanamine Dimethyl-[2-(3,4,6,7-tetramethoxyphenanthren-1-yl)ethyl]azanium Dimethyl(2-naphtho[2,1-g][1,3]benzodioxol-5-ylethyl)azanium 8-[2-(dimethylamino)ethyl]-9,10-dihydrophenanthrene-3,4-diol;hydron;bromide N,N-dimethyl-2-pyren-1-ylpropan-1-amine 2-(3,4-Dihydroxyphenanthren-1-yl)ethyl-trimethylazanium N,N-dimethyl-2-[(6R)-6-methyl-6,7-dihydronaphtho[2,1-g][1,3]benzodioxol-5-yl]ethanamine N,N-dimethyl-2-(3,4,6,7-tetramethoxy-6,7-dihydrophenanthren-1-yl)ethanamine N,N-dimethyl-2-[(10R)-3,4,6,7-tetramethoxy-10-methyl-9,10-dihydrophenanthren-1-yl]ethanamine Trimethyl(2-naphtho[2,1-g][1,3]benzodioxol-5-ylethyl)azanium Ethyl-methyl-(2-phenanthro[3,4-d][1,3]dioxol-5-yl-ethyl)-amine (1S)-2-(dimethylamino)-1-naphtho[2,1-g][1,3]benzodioxol-5-ylethanol Trimethyl-[2-(2,3,4-trimethoxyphenanthren-1-yl)ethyl]azanium 3,6-Dimethoxy-4-hydroxy-8-<2-(N-methyl-N-ethylamino)ethyl>phenanthrene [2-(5,6-dimethoxy-9,10-dihydro-[1]phenanthryl)-ethyl]-dimethyl-amine 8-[2-(Dimethylamino)ethyl]-3,5-dimethoxyphenanthrene-2,6-diol 2-bromosecoboldine 2-bromo-N,N-dimethylsecoboldine iodide 2-bromo-3,7-dimethoxy-N,N-dimethylsecoboldine iodide 2-bromo-N-methylsecoboldine