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长春胺杂质 | 32790-09-3

中文名称
长春胺杂质
中文别名
——
英文名称
Δ14-vincamine
英文别名
Δ17-vincamine;(+)-14,15-didehydrovincamine;(+)-14,15-dehydrovincamine;14,15-didehydrovincamine;17,18-didehydrovincamine;14,15-dehydro vincamine;17,18-Dehydrovincamine;methyl (15R,17S,19S)-15-ethyl-17-hydroxy-1,11-diazapentacyclo[9.6.2.02,7.08,18.015,19]nonadeca-2,4,6,8(18),13-pentaene-17-carboxylate
长春胺杂质化学式
CAS
32790-09-3
化学式
C21H24N2O3
mdl
——
分子量
352.433
InChiKey
BQGJXFQCMYJENQ-GIVPXCGWSA-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

  • 熔点:
    224-225 °C
  • 沸点:
    508.7±50.0 °C(Predicted)
  • 密度:
    1.35±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.8
  • 重原子数:
    26
  • 可旋转键数:
    3
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.48
  • 拓扑面积:
    54.7
  • 氢给体数:
    1
  • 氢受体数:
    4

SDS

SDS:32a21df4d35e9b9a90e0cbcefbda8121
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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:
    长春胺杂质potassium iodate 、 sodium cyanoborohydride 、 溶剂黄146 作用下, 以 1,4-二氧六环溶剂黄146 为溶剂, 反应 26.5h, 生成 长春胺
    参考文献:
    名称:
    亚甲基二氢吲哚,吲哚啉和吲哚鎓-XII:脱水的半合成-14,15长春胺等
    摘要:
    DOI:
    10.1016/0040-4020(80)80026-3
  • 作为产物:
    描述:
    methyl (6aR,11aS,12S,13aR)-13a-ethyl-5,6,13,13a-tetrahydro-3H,11H-12,6a-(epoxyimino)cyclopenta[ij]indolo[2,3-a]quinolizine-12(41H)-carboxylate 在 亚硝酸特丁酯溶剂黄146 作用下, 以 四氢呋喃 为溶剂, 反应 8.17h, 生成 长春胺杂质
    参考文献:
    名称:
    Oxidation of .beta.-anilinoacrylate alkaloids vincadifformine and tabersonine by Fremy's salt. A mechanistic insight into the rearrangement of Aspidosperma to Hunteria eburnea alkaloids
    摘要:
    DOI:
    10.1021/jo00240a023
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文献信息

  • Synthesis of vinca alakaloids and realated compounds<b>98</b>. Oxidation with dimethyldioxirane of compounds containing the aspidospermane and quebrachamine ring system. A simple synthesis of (7<i>S</i>,20<i>S</i>)-(+)-rhazidigenine and (2<i>R</i>,7<i>S</i>,20<i>S</i>)-(+)-rhazidine
    作者:János Éles、György Kalaus、Lajos SzabÓ、Albert LÉvai、IstvÁn Greiner、MÁria KajtÁr-Peredy、PÁl SzabÓ、Csaba SzÁntay
    DOI:10.1002/jhet.5570390423
    日期:2002.7
    The oxidation of (-)-tabersonine (1) with dimethyldioxirane (DMD) in neutral and acidic medium gave 16-hydroxytabersonine-N-oxide (3) and the didehydrovincamine isomers 4 and 5, respectively. (+)-14,15-Didehydro-quebrachamine (7) furnished the hydroxyindolenine 9, and the pentacyclic derivative 11. (+)-Quebrachamine (8) and DMD in neutral medium gave (7S,20S)-(+)-rhazidigenine (12) which was converted
    在中性和酸性介质中,用二甲基二环氧乙烷(DMD)氧化(-)-大黄碱(1)分别得到16-羟基大黄碱-N-氧化物(3)和二脱氢长春胺异构体4和5。(+)-14,15-Didehydro-quebrachamine(7)提供了羟基吲哚啉9和五环衍生物11。(+)-瓜拉巴胺(8)和DMD在中性介质中得到(7 S,20 S)-(+)-rhazidigenine(12),将其转化为(2 R,7 S,20 S)-(+)-rhazidine (13b)用盐酸。
  • Ozonation in alkoloid chemistry: a mild and selective conversion of vincadifformine into vincamine
    作者:Bruno Danieli、Giordano Lesma、Giovanni Palmisano、Bruno Gabetta
    DOI:10.1039/c39810000908
    日期:——
    Vincamine has been obtained in a ‘one-pot’ method by ozonation of vincadifformine.
    长春花碱的臭氧化是通过“一锅法”获得的。
  • Synthesis of 18-Hydroxyvincamines and Epoxy-1,14-secovincamines; a New Proof for the Aspidospermane-Eburnane Rearrangement
    作者:András Nemes、Csaba Szántay、László Czibula、István Greiner
    DOI:10.3987/com-07-11114
    日期:——
    Chemical transformations started from tabersonine were studied. A one-pot oxidative ring-transformation with permaleic acid in methanol yielded 17,18-dehydrovincamine. Hydroboration-oxidation of the latter compound led to alkaloid 17,18-dehydrovincamone. Hydroboration-oxidation of tabersonine resulted 14 beta-hydroxyvineadifformine and 15p-hydroxyvincadifforinine. Allowing 14 beta- and 15 beta- hydroxyvincadifformines to react with permaleic acid/methanol provided 1,14-secovincamines, serving as new evidence for the mechanism of the aspidospermane-eburnane transformation. On the other hand 18 beta-hydroxyvincamine was obtained from 14 beta-hydroxyvincadifformine by reaction with 3-chloroperbenzoic acid and successive treatment with triphenylphosphine/aqueous acetic acid.
  • Calabi, Luisella; Danieli, Bruno; Lesma, Giordano, Journal of the Chemical Society. Perkin transactions I, 1982, p. 1371 - 1380
    作者:Calabi, Luisella、Danieli, Bruno、Lesma, Giordano、Palmisano, Giovanni
    DOI:——
    日期:——
  • Lewin, Guy; Rolland, Yves; Poisson, Jacques, Heterocycles, 1980, vol. 14, # 12, p. 1915 - 1920
    作者:Lewin, Guy、Rolland, Yves、Poisson, Jacques
    DOI:——
    日期:——
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同类化合物

阿扑长春胺 长春醇 长春酸胺 长春西汀杂质N 长春西汀杂质L 长春西汀杂质K 长春西汀杂质J 长春西汀杂质I 长春西汀杂质27 长春西汀杂质1 长春西汀杂质 A 长春西汀 长春胺杂质 长春胺杂质 长春胺乙酯 长春胺 长春泊林 长春布宁 长春倍酯 长春乙酯羧酸 象牙酮宁 溴长春胺 富马酸溴长春胺 埃那胺 7-氨基-4-羟基-3-(苯偶氮基)萘-2-磺基酸 14,15-二氢阿扑长春胺乙酯 13alpha-乙基-2,3,5,6,13a,13b-六氢-1H-吲哚并(3,2,1-去)吡啶并(3,2,1-ij)(1,5)-萘啶-12-羧酸甲氧基甲基酯 (3alpha,16alpha)-6-羟基-象牙洪达木烯宁-14(15H)-酮 (3alpha,14beta,16alpha)-14,15-二氢-14-羟基埃那美宁-14-甲醇 (+)-(14beta)-二氢长春西丁 (+/-)-vincaminine (3α)-Eburnamenine-14-carbonyl chloride hydrochloride (-)-3S,16R-14-benzoyloxymethyl-eburnamenine apovincamine acetylsalicylate (+)-vinpocetine-9,11-disulfonic acid (3-methoxypropyl)diamide 14-(aminomethyl)-vincane O-((eburnamenine-14-yl)methyl)(4-methoxyphenyl)carbamothioate O-((eburnamenine-14-yl)methyl)(4-chlorophenyl)carbamothioate O-((eburnamenine-14-yl)methyl)(morpholine-4-carbonyl)(phenyl)carbamothioate (+)-14-carboxy-eburnamenine(3,16)-10-sulfonamide vinpocetine hydrochloride (+)-14-(2-chloro)carboethoxy-eburnamenine(3,16)-10-sulfonic acid (3-methoxypropyl)amide (+)-14-carbopropyloxy-eburnamenine(3,16)-10-sulfonic acid (3-methoxypropyl)amide (+)-apovincamine-10-sulfonic acid (3-methoxypropyl)amide 4-oxide 6-hydroxy-py-tetrahydroapovincamine chloride 10-nitro-6-oxovincamine (41S,13aS)-13a-ethyl-N,N-dimethyl-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5] naphthyridine-12-carboxamide N-(((41S,13aS)-13a-ethyl-2,3,41,5,6,13a-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-yl)methyl)isobutyramide vincamine acetylsalicylate 6-hydroxy-py-tetrahydro-16-deoxyepivincamine chloride