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(+/-)-erythro-isocordrastine | 55219-41-5

中文名称
——
中文别名
——
英文名称
(+/-)-erythro-isocordrastine
英文别名
(+/-)-isocordrastine II;erythro-isocordrastine;(RS)-3-((SR)-6,7-dimethoxy-2-methyl-1,2,3,4-tetrahydro-isoquinolin-1-yl)-5,6-dimethoxy-3H-isobenzofuran-1-one;(3R)-3-[(1S)-6,7-dimethoxy-2-methyl-3,4-dihydro-1H-isoquinolin-1-yl]-5,6-dimethoxy-3H-2-benzofuran-1-one
(+/-)-erythro-isocordrastine化学式
CAS
55219-41-5;55563-22-9;59122-81-5;59433-41-9;59433-42-0
化学式
C22H25NO6
mdl
——
分子量
399.444
InChiKey
LMYSPOQJHNXRKZ-LEWJYISDSA-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):
    2.9
  • 重原子数:
    29
  • 可旋转键数:
    5
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.41
  • 拓扑面积:
    66.5
  • 氢给体数:
    0
  • 氢受体数:
    7

反应信息

  • 作为产物:
    描述:
    6'-溴二氢罂粟碱 在 sodium tetrahydroborate 、 三甲基氯硅烷 、 Pd(PPh3)(OAc)2 、 氧气亚甲兰potassium carbonate 作用下, 以 甲醇二氯甲烷溶剂黄146甲苯乙腈 为溶剂, 反应 26.25h, 生成 (+/-)-erythro-isocordrastine
    参考文献:
    名称:
    钯(0)催化羰基化反应的不同途径合成邻苯二甲酰异喹啉和小ber碱生物碱和吲哚[2,1-a]异喹啉(1)。
    摘要:
    通过在含碳酸钾的N,N-二甲基甲酰胺中加热得到2,3,8,9-或2,3,9,10-烷氧基取代的5,6-来实现赤氨基氨基醇19的一锅环化。 dihydroindolo [2,1-a] isoquinolines 3,具有二苯并吡咯啉碱生物碱的独特四环骨架特征。类似地,发现在过量碳酸钾存在下,钯(0)催化1-(2'-溴苄基)四氢异喹啉21的羰基化反应生成8-氧代berbines 22,经氢化铝锂还原后可转化为原小ber碱生物碱4 。具有二苯并吡咯啉碱生物碱的独特四环骨架特征。类似地,发现在过量碳酸钾存在下,钯(0)催化1-(2'-溴苄基)四氢异喹啉21的羰基化反应生成8-氧代berbines 22,经氢化铝锂还原后可转化为原小ber碱生物碱4 。具有二苯并吡咯啉碱生物碱的独特四环骨架特征。类似地,发现在过量碳酸钾存在下,钯(0)催化1-(2'-溴苄基)四氢异喹啉21的羰基化反应生成8-氧代berbines
    DOI:
    10.1021/jo982451w
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文献信息

  • Studies on carboxylation of alkoxy-substituted benzyl alcohols via direct lithiation and bromine-lithium exchange: Synthesis of phthalides and phthalideisoquinoline alkaloids
    作者:Kazuhiko Orito、Mamoru Miyazawa、Hiroshi Suginome
    DOI:10.1016/0040-4020(95)00003-q
    日期:1995.2
    Conversion of alkoxy-substituted benzyl alcohols to the corresponding phthalides by carboxylation via ortho lithiation and bromine-lithium exchange was studied. The method was applied to the key step in the synthesis of phthalideisoquinoline alkaloids.
    研究了通过邻位锂化和溴-锂交换通过羧化将烷氧基取代的苄醇转化为相应的邻苯二甲酸酯。该方法应用于邻苯二甲酰异喹啉生物碱的合成关键步骤。
  • Slemon, Clarke E.; Hellwig, Louise C.; Ruder, Jean-Pierre, Canadian Journal of Chemistry, 1981, vol. 59, p. 3055 - 3060
    作者:Slemon, Clarke E.、Hellwig, Louise C.、Ruder, Jean-Pierre、Hoskins, Eric W.、MacLean, David B.
    DOI:——
    日期:——
  • Kametani,T. et al., Heterocycles, 1975, vol. 3, p. 1091 - 1098
    作者:Kametani,T. et al.
    DOI:——
    日期:——
  • Marsden, Richard; MacLean, David B., Canadian Journal of Chemistry, 1984, vol. 62, p. 306 - 308
    作者:Marsden, Richard、MacLean, David B.
    DOI:——
    日期:——
  • Synthesis of Phthalideisoquinoline and Protoberberine Alkaloids and Indolo[2,1-<i>a</i>]isoquinolines in a Divergent Route Involving Palladium(0)-Catalyzed Carbonylation<sup>1</sup>
    作者:Kazuhiko Orito、Mamoru Miyazawa、Ryo Kanbayashi、Masao Tokuda、Hiroshi Suginome
    DOI:10.1021/jo982451w
    日期:1999.9.1
    hydride in tetrahydrofuran gave the threo-isomer 20 in preference to the erythro 19. On the basis of studies on palladium(0)-catalyzed carbonylation of 2-bromo-3,4-dimethoxybenzyl alcohol to 6,7-dimethoxyphthalide, amino alcohol 19 or 20 was treated with a catalytic amount of palladium(II) acetate and triphenylphosphine in an atmosphere of carbon monoxide in the presence of chlorotrimethylsilane and potassium
    通过在含碳酸钾的N,N-二甲基甲酰胺中加热得到2,3,8,9-或2,3,9,10-烷氧基取代的5,6-来实现赤氨基氨基醇19的一锅环化。 dihydroindolo [2,1-a] isoquinolines 3,具有二苯并吡咯啉碱生物碱的独特四环骨架特征。类似地,发现在过量碳酸钾存在下,钯(0)催化1-(2'-溴苄基)四氢异喹啉21的羰基化反应生成8-氧代berbines 22,经氢化铝锂还原后可转化为原小ber碱生物碱4 。具有二苯并吡咯啉碱生物碱的独特四环骨架特征。类似地,发现在过量碳酸钾存在下,钯(0)催化1-(2'-溴苄基)四氢异喹啉21的羰基化反应生成8-氧代berbines 22,经氢化铝锂还原后可转化为原小ber碱生物碱4 。具有二苯并吡咯啉碱生物碱的独特四环骨架特征。类似地,发现在过量碳酸钾存在下,钯(0)催化1-(2'-溴苄基)四氢异喹啉21的羰基化反应生成8-氧代berbines
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同类化合物

阿托喹啉 那可汀 那可丁N-氧化物 诺司卡品 盐酸盐 水合物 细果角茴香碱 紫堇明 盐酸那可丁一水合物 盐酸诺格考平 盐酸白毛莨碱 曲托喹啉 山缘草定碱 咖喏定 北美黄连碱 [S-(R*,R*)]-6,7-二甲氧基-3-(5,6,7,8-四氢-4-羟基-6-甲基-1,3-二氧杂环戊并[4,5-g]异喹啉-5-基)苯酞 [6S,(+)]-6-[(1S)-1,2,3,4-四氢-6,7-二甲氧基-2-甲基异喹啉-1-基]呋喃并[3,4-e]-1,3-苯并二氧戊环-8(6H)-酮 7-氨基-4,5,6-三乙氧基-3-(6,7,8-三甲氧基-2-甲基-3,4-二氢-1H-异喹啉-1-基)-3H-2-苯并呋喃-1-酮 7-O-去甲基alpha-那可丁 6,7-二甲氧基-3-[(5R)-4-甲氧基-6-甲基-7,8-二氢-5H-[1,3]二氧杂环戊并[4,5-g]异喹啉-5-基]-3H-2-苯并呋喃-1-酮 3-异喹啉-1-基-3H-2-苯并呋喃-1-酮 (3S)-6,7-二甲氧基-3-[(5S)-6-甲基-5,6,7,8-四氢[1,3]二氧杂环戊并[4,5-g]异喹啉-5-基]-2-苯并呋喃-1(3H)-酮 (3S)-3-[(1R)-6,7-二羟基-8-甲氧基-2-甲基-3,4-二氢-1H-异喹啉-1-基]-6,7-二甲氧基-3H-2-苯并呋喃-1-酮 (-)-荷苞牡丹碱甲溴化物 (-)-荷苞牡丹碱 (-)-荷包牡丹碱甲溴化物 (-)-荷包牡丹碱甲氯化物 (-)-紫堇明 (+)-荷苞牡丹碱甲氯化物 (+)-荷包牡丹碱 hydrastidine isohydrastidine 5,9-bis-(4,5-dimethoxy-3-oxo-phthalan-1-yl)-4-methoxy-6-methyl-5,6,7,8-tetrahydro-[1,3]dioxolo[4,5-g]isoquinoline (S,R)-9-bromo noscapine (S)-3-{(R)-9-[(2-chloro-acetylamino)-methyl]-4-methoxy-6-methyl-5,6,7,8-tetrahydro-[1,3]dioxolo[4,5-g]isoquinolin-5-yl}-6,7-dimethoxy-phthalide (S)-6,7-dimethoxy-3-{(R)-4-methoxy-6-methyl-9-[(2-morpholino-acetylamino)-methyl]-5,6,7,8-tetrahydro-[1,3]dioxolo[4,5-g]isoquinolin-5-yl}-phthalide (R)-5-((S)-4,5-dimethoxy-3-oxo-phthalan-1-yl)-4-methoxy-6-methyl-5,6,7,8-tetrahydro-[1,3]dioxolo[4,5-g]isoquinoline-9-carboxylic acid methyl ester 4-(((S)-1-((R)-9-bromo-4-methoxy-6-methyl-5,6,7,8-tetrahydro-[1,3]dioxolo[4,5-g]isoquinolin-5-yl)-5-methoxy-3-oxo-1,3-dihydroisobenzofuran-4-yl)oxy)butane-1-sulfonic acid ethyl 4-((5R)-5-((1S)-4,5-dimethoxy-3-oxo-1,3-dihydroisobenzofuran-1-yl)-4-methoxy-6-methyl-5,6,7,8-tetrahydro-[1,3]dioxolo[4,5-g]isoquinolin-9-yl)benzoate N-(3-((5R)-5-((1S)-4,5-dimethoxy-3-oxo-1,3-dihydroisobenzofuran-1-yl)-4-methoxy-6-methyl-5,6,7,8-tetrahydro-[1,3]dioxolo[4,5-g]isoquinolin-9-yl)phenyl)acetamide (S)-3-((R)-9-bromo-4-methoxy-6-methyl-5,6,7,8-tetrahydro-[1,3]dioxolo[4,5-g]isoquinolin-5-yl)-7-hydroxy-6-methoxyisobenzofuran-1(3H)-one ethyl 2-chloro-5-((5R)-5-((1S)-4,5-dimethoxy-3-oxo-1,3-dihydroisobenzofuran-1-yl)-4-methoxy-6-methyl-5,6,7,8-tetrahydro-[1,3]dioxolo[4,5-g]isoquinolin-9-yl)benzoate 3-(((S)-1-((R)-9-bromo-4-methoxy-6-methyl-5,6,7,8-tetrahydro-[1,3]dioxolo[4,5-g]isoquinolin-5-yl)-5-methoxy-3-oxo-1,3-dihydroisobenzofuran-4-yl)oxy)propane-1-sulfonic acid 4-(((S)-5-methoxy-1-((R)-4-methoxy-6-methyl-5,6,7,8-tetrahydro-[1,3]dioxolo[4,5-g]isoquinolin-5-yl)-3-oxo-1,3-dihydroisobenzofuran-4-yl)oxy)butane-1-sulfonic acid (3S)-6,7-dimethoxy-3-((5R)-4-methoxy-6-methyl-9-(4-vinylphenyl)-5,6,7,8-tetrahydro-[1,3]dioxolo[4,5-g]isoquinolin-5-yl)isobenzofuran-1(3H)-one (R)-5-((S)-4,5-dimethoxy-3-oxo-1,3-dihydroisobenzofuran-1-yl)-4-methoxy-6-methyl-5,6,7,8-tetrahydro[1,3]dioxolo[4,5-g]isoquinoline-9-carbaldehyde N-desmethyl-N-carbethoxynarcotine (S)-3-((R)-9-bromo-4-methoxy-5,6,7,8-tetrahydro-[1,3]dioxolo[4,5-g]isoquinolin-5-yl)-6,7-dimethoxyisobenzofuran-1(3H)-one 9-Fluoro-Noscapine 9-Nitro-Noscapine 7-benzyloxy-6-methoxy-3-(4-methoxy-6-methyl-5,6,7,8-tetrahydro-[1,3]dioxolo[4,5-g]isoquinolin-5-yl)-3H-isobenzofuran-1-one 7-benzyloxy-6-methoxy-3-(4-methoxy-6-methyl-5,6,7,8-tetrahydro-[1,3]dioxolo[4,5-g]isoquinolin-5-yl)-3H-isobenzofuran-1-one