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N-Pent-4-enoylemetine | 163926-93-0

中文名称
——
中文别名
——
英文名称
N-Pent-4-enoylemetine
英文别名
1-[(1R)-1-[[(2R,3R,11bS)-3-ethyl-9,10-dimethoxy-2,3,4,6,7,11b-hexahydro-1H-benzo[a]quinolizin-2-yl]methyl]-6,7-dimethoxy-3,4-dihydro-1H-isoquinolin-2-yl]pent-4-en-1-one
N-Pent-4-enoylemetine化学式
CAS
163926-93-0
化学式
C34H46N2O5
mdl
——
分子量
562.75
InChiKey
OTLMHQIAGIIIBP-CRKZPIATSA-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

物化性质

  • 沸点:
    684.6±55.0 °C(Predicted)
  • 密度:
    1.17±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    5.7
  • 重原子数:
    41
  • 可旋转键数:
    10
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.56
  • 拓扑面积:
    60.5
  • 氢给体数:
    0
  • 氢受体数:
    6

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:
    N-Pent-4-enoylemetine 作用下, 以 四氢呋喃 为溶剂, 反应 6.0h, 以92%的产率得到依米丁
    参考文献:
    名称:
    The Pent-4-enoyl Group: A Novel Amine-Protecting Group That Is Readily Cleaved under Mild Conditions
    摘要:
    Primary and secondary amines are readily protected as N-pent-4-enoyl derivatives, the resulting N-pent-4-enamides being usually highly crystalline. Deprotection is rapidly and efficiently effected under mild conditions by treatment with 3 equiv of iodine in aqueous THF solution. Although an oxidizing medium, these deprotection conditions do not affect oxidizable functionalities including p-methoxybenzyl ethers and alkyl sulfides.
    DOI:
    10.1021/jo00129a036
  • 作为产物:
    描述:
    4-戊烯酰氯吡啶三乙胺 作用下, 以 甲醇二氯甲烷 为溶剂, 反应 0.83h, 生成 N-Pent-4-enoylemetine
    参考文献:
    名称:
    The Pent-4-enoyl Group: A Novel Amine-Protecting Group That Is Readily Cleaved under Mild Conditions
    摘要:
    Primary and secondary amines are readily protected as N-pent-4-enoyl derivatives, the resulting N-pent-4-enamides being usually highly crystalline. Deprotection is rapidly and efficiently effected under mild conditions by treatment with 3 equiv of iodine in aqueous THF solution. Although an oxidizing medium, these deprotection conditions do not affect oxidizable functionalities including p-methoxybenzyl ethers and alkyl sulfides.
    DOI:
    10.1021/jo00129a036
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文献信息

  • Two New Orthogonal Amine-Protecting Groups that can be Cleaved under Mild or Neutral Conditions
    作者:John S. Debenham、Robert Madsen、Carmichael Roberts、Bert Fraser-Reid
    DOI:10.1021/ja00116a047
    日期:1995.3
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同类化合物

盐酸吐根酚碱 盐酸吐根碱 吐根碱氢溴酸盐 吐根碱氢溴酸盐 吐根碱 依米丁二盐酸盐水合物 依米丁 二盐酸吐根碱 九节碱 7',10,11-三甲氧基-1',2'-二去氢依米丁-6'-醇草酸盐(1:1) 2-[(6,7-二甲氧基-1,2,3,4-四氢异喹啉-1-基)甲基]-3-乙基-9,10-二甲氧基-2,3,4,6,7,11b-六氢-1H-吡啶并[2,1-a]异喹啉四水合物二盐酸盐 1',2'-二去氢-7',10,11-三甲氧基依米丁-6',9-二醇 (+)-吐根素二盐酸盐水合物 N-Phthaloyl-phenylalanyl-emetin N-Phthaloyl-glycyl-emetin 2'-heptyl-10,11,6',7'-tetramethoxy-emetane Alangamid-methylether (2R,12bS)3-Ethyl-2-(3,4-dihydro-6,7-dimethoxy-isochinolinyl-(1)-methyl)-1,2,3,4,6,7,12,12b-octahydro-indolo<2,3-a>-chinolizin (2R,3R,11bS)-(+)-9-benzyloxy-2-(6-benzyloxy-3,4-dihydro-7-methoxy-1-isoquinolyl)methyl-3-ethyl-1,3,4,6,7,11b-hexahydro-10-methoxy-2H-benzoquinolizine 1-ethyl-10,11,6',7'-tetramethoxy-16,17-dinor-emetane Pharmakon1600-01500272 2'-Benzoyl-10,11,6',7'-tetramethoxy-1'αH-emetan bis-(10,11,6',7'-tetramethoxy-emetan-2'-yl)-methane N-Methylol-cephaelin (2R,3R,12bS)-2-(6,7-Dimethoxy-3,4-dihydro-isoquinolin-1-ylmethyl)-3-ethyl-1,2,3,4,6,7,12,12b-octahydro-indolo[2,3-a]quinolizine Glycyl-emetin 2-(6,7-Dimethoxy-1,2,3,4-tetrahydro-isoquinolin-1-ylmethyl)-3-ethyl-9,10-dimethoxy-1,3,4,6,7,11b-hexahydro-2H-pyrido[2,1-a]isoquinoline; compound with 3,4-dichloro-benzenesulfonic acid Psychotrine tetrahydrate Psychotrine sulfate trihydrate (+/-)-N-(3-Hydroxy-butyl)-emetin Psychotrine sulfate 10,11,6',7'-tetramethoxy-emetane-2'-carboxylic acid ethyl ester 2-(6,7-Dimethoxy-1,2,3,4-tetrahydro-isoquinolin-1-ylmethyl)-3-ethyl-9,10-dimethoxy-1,3,4,6,7,11b-hexahydro-2H-pyrido[2,1-a]isoquinoline; compound with 4-benzyloxy-benzenesulfonic acid (2R,3S,12bS)-2-(6,7-Dimethoxy-3,4-dihydro-isoquinolin-1-ylmethyl)-3-ethyl-1,2,3,4,6,7,12,12b-octahydro-indolo[2,3-a]quinolizine 3-Acetyl-2-<2-butyl-1.2.3.4-tetrahydro-6.7-dimethoxy-isochinolyl-(1)-methyl>-1.2.3.4.6.7-hexahydro-9.10-dimethoxy-11bH-benzochinolizin-aethylendithioketal N-Chloracetyl-emetin 11b-epi-O-methylpsychotrine