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21-cyanocatharanthine | 82622-21-7

中文名称
——
中文别名
——
英文名称
21-cyanocatharanthine
英文别名
methyl (1S,15R,18R)-18-cyano-17-ethyl-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4,6,8,16-pentaene-1-carboxylate
21-cyanocatharanthine化学式
CAS
82622-21-7
化学式
C22H23N3O2
mdl
——
分子量
361.444
InChiKey
HCVOUSXZJPNPAN-GAQQMNMRSA-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):
    2.6
  • 重原子数:
    27
  • 可旋转键数:
    3
  • 环数:
    6.0
  • sp3杂化的碳原子比例:
    0.45
  • 拓扑面积:
    69.1
  • 氢给体数:
    1
  • 氢受体数:
    4

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
  • 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:
    21-cyanocatharanthine间氯过氧苯甲酸 作用下, 以 二氯甲烷 为溶剂, 反应 0.17h, 以61%的产率得到methyl (13Z)-18-cyano-17-ethyl-16-hydroxy-13-oxido-3-aza-13-azoniatetracyclo[13.3.1.02,10.04,9]nonadeca-2(10),4,6,8,13,17-hexaene-1-carboxylate
    参考文献:
    名称:
    Rearrangement of catharanthine. (V). 21-Cyanocatharanthine
    摘要:
    DOI:
    10.1021/jo00143a017
  • 作为产物:
    描述:
    长春质碱三甲基氰硅烷 在 lithium perchlorate 作用下, 以 为溶剂, 以3%的产率得到3-cyanocatharanthine
    参考文献:
    名称:
    Oxidative fragmentation of catharanthine by dichlorodicyanoquinone
    摘要:
    Oxidation of catharanthine by DDQ leads to formation of products resulting from fragmentation of the C16-C21 bond as well as C3 and C5 dehydrogenation. Among the products are compounds containing a cyclopropane ring formed by bonding between C14 and C16. Cyclopropane ring formation can be also be observed from the intermediate generated by Potier-Polonovski fragmentation of catharanthine N-oxide.
    DOI:
    10.1021/jo00005a007
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文献信息

  • Oxidative fragmentation of catharanthine by dichlorodicyanoquinone
    作者:Richard J. Sundberg、Phyllis J. Hunt、Patrice Desos、Kumar G. Gadamasetti
    DOI:10.1021/jo00005a007
    日期:1991.3
    Oxidation of catharanthine by DDQ leads to formation of products resulting from fragmentation of the C16-C21 bond as well as C3 and C5 dehydrogenation. Among the products are compounds containing a cyclopropane ring formed by bonding between C14 and C16. Cyclopropane ring formation can be also be observed from the intermediate generated by Potier-Polonovski fragmentation of catharanthine N-oxide.
  • Rearrangement of catharanthine. (V). 21-Cyanocatharanthine
    作者:P. Mangeney、N. Langlois、C. Leroy、C. Riche、Y. Langlois
    DOI:10.1021/jo00143a017
    日期:1982.10
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同类化合物

马山茶碱 非洲伏康树碱 长春质碱 老刺木任 硫酸长春质碱 海尼山辣椒碱羟基假吲哚 榴花碱 柳黄酸 伏康京碱 伊菠胺-18-羧酸甲酯 伊菠胺 伊菠加因盐酸盐 伊博格碱 7-羟基-1-去氢老刺木碱 20-羟基榴花碱 14-((3alpha)-17-甲氧基-17-氧代派利文碱-3-基)-伊菠胺-18-羧酸甲酯 13-甲氧基-14-[(3A)-17-甲氧基-17-氧代派利文碱-3-基]-伊菠胺-18-羧酸甲酯 13-甲氧基-12-[(3a)-17-甲氧基-17-氧代派利文碱-3-基]-伊菠胺-18-羧酸甲酯 12-((3alpha)-17-甲氧基-17-氧代派利文碱-3-基)-伊菠胺-18-羧酸甲酯 11-羟基狗牙花定 10-羟基狗牙花定 (4a,20S)-20-羟基伊菠胺-18-羧酸甲酯 (2S)-1,2,3,4,4abeta,5,6,7,7a,12bbeta-十氢-4alpha-(1-羟基乙基)-9-甲氧基-2alpha,5alpha-甲桥吲哚并[3,2-d][1]苯并氮杂卓-7alpha-醇 epiibogaine N-methylcatharanthine quaternary salt lauryl albifloranine (+/-)-Coronaridine 18-methoxycoronaridine hydrochloride voacangine 19-Ethoxycoronaridin N-methylibogaine 2-(dimethylamino)ethyl (1R,15R,17S,18S)-17-ethyl-7-hydroxy-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4(9),5,7-tetraene-3-carboxylate ethyl (1R,15R,17S,18S)-17-ethyl-7-hydroxy-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4(9),5,7-tetraene-3-carboxylate [(1R,15R,17S,18S)-3-dimethoxyphosphoryl-17-ethyl-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4(9),5,7-tetraen-7-yl] 4-methylpiperazine-1-carboxylate hydron;methyl (1S,15R,17S,18S)-17-ethyl-14-hydroxy-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4,6,8-tetraene-1-carboxylate;chloride eglandine Ibogamine-18-carboxylic acid, 19-hydroxy-12-methoxy-, methyl ester, (19R)- 3-(beta-Hydroxyethyl)coronaridine Ibogamine-18-carboxylic acid, 13,20-dihydroxy-, methyl ester, (4alpha,20S)- 10-Hydroxyheyneanine Ibogamine-18-carboxylic acid, 21-hydroxy-, methyl ester Ibogamin-20-ol, 8,19-epoxy-12-methoxy-, (4alpha,8beta,19S,20S)- Voacangine Conopharyngine ibogaline (+/-)-coronaridine (-)-Ibogaine (15S,17R)-17-ethyl-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4,6,8-tetraene (15S,17R)-17-ethyl-7-methoxy-3-methyl-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4(9),5,7-tetraene Voacangine 11-(3,4-dimethoxybenzyl)