摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

ethyl‑2‑amino‑5′‑bromo‑7,7‑dimethyl‑2′,5‑dioxo‑5,6,7,8‑tetrahydrospiro [chromene‑4,3'‑indoline]‑3‑carboxylate | 336181-03-4

中文名称
——
中文别名
——
英文名称
ethyl‑2‑amino‑5′‑bromo‑7,7‑dimethyl‑2′,5‑dioxo‑5,6,7,8‑tetrahydrospiro [chromene‑4,3'‑indoline]‑3‑carboxylate
英文别名
ethyl 2-amino-5′-bromo-7,7-dimethyl-2′,5-dioxo-5,6,7,8-tetrahydrospiro[chromene-4,3′-indoline]-3-carboxylate;ethyl 2-amino-5'-bromo-7,7-dimethyl-2',5-dioxo-1',2',5,6,7,8-hexahydrospiro[chromene-4,3'-indole]-3-carboxylate;ethyl 2-amino-5'-bromo-7,7-dimethyl-2',5-dioxo-5,6,7,8-tetrahydrospiro[chromene-4,3'-indoline]-3-carboxylate;ethyl 2-amino-5'-bromo-7,7-dimethyl-5-oxo-5,6,7,8-tetrahydrospiro[chromene-4,3'-indole]-2'-one-3-carboxylate;ethyl 2-amino-5'-bromo-7,7-dimethyl-2',5-dioxo-5,6,7,8-tetrahydrospiro[chromene-4,3-indoline]-3-carboxylate;ethyl 2'-amino-5-bromo-7',7'-dimethyl-2,5'-dioxospiro[1H-indole-3,4'-6,8-dihydrochromene]-3'-carboxylate
ethyl‑2‑amino‑5′‑bromo‑7,7‑dimethyl‑2′,5‑dioxo‑5,6,7,8‑tetrahydrospiro [chromene‑4,3'‑indoline]‑3‑carboxylate化学式
CAS
336181-03-4
化学式
C21H21BrN2O5
mdl
——
分子量
461.312
InChiKey
LMYRMERUWOGLNI-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

物化性质

  • 熔点:
    260-262 °C
  • 沸点:
    664.6±55.0 °C(Predicted)
  • 密度:
    1.57±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.7
  • 重原子数:
    29
  • 可旋转键数:
    3
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.38
  • 拓扑面积:
    108
  • 氢给体数:
    2
  • 氢受体数:
    6

反应信息

  • 作为产物:
    描述:
    5-溴靛红5,5-二甲基-1,3-环己二酮氰乙酸乙酯三乙胺 作用下, 以 乙醇 为溶剂, 反应 0.08h, 以95%的产率得到ethyl‑2‑amino‑5′‑bromo‑7,7‑dimethyl‑2′,5‑dioxo‑5,6,7,8‑tetrahydrospiro [chromene‑4,3'‑indoline]‑3‑carboxylate
    参考文献:
    名称:
    A Facile Synthesis of Some Spirooxoindole Derivatives via One-Pot Three-Component Reactions
    摘要:
    合成了四氢螺[色烯-4,3-吲哚]-2-酮(5a-c)和螺[吲哚-3,4-吡喃(3,2-d)吡唑]-2-酮(6a-b)基于5-(未)取代靛红(1a-c)与氰基乙酸乙酯(2)和5,5-二甲基环己烷-1,3-二酮(3)或5-甲基-的一锅三组分环缩合反应2-苯基-2,4-二氢-吡唑-3-酮(4)在含有催化量的Et3N的无水乙醇中在常规加热和环境友好的程序下进行。所得化合物的结构通过光谱{IR、1H NMR、13C NMR、2D NMR [1H-1H COSY、1H-13C COSY (HETCOR)]和电喷雾电离串联质量[(±) ESI-MS/MS]确认} 分析。
    DOI:
    10.14233/ajchem.2013.14270
点击查看最新优质反应信息

文献信息

  • Silica-bonded 5-n-propyl-octahydro-pyrimido[1,2-a]azepinium chloride (SB-DBU)Cl as a highly efficient, heterogeneous and recyclable silica-supported ionic liquid catalyst for the synthesis of benzo[b]pyran, bis(benzo[b]pyran) and spiro-pyran derivatives
    作者:Alireza Hasaninejad、Nooshin Golzar、Maryam Beyrati、Abdolkarim Zare、Mohammad Mahdi Doroodmand
    DOI:10.1016/j.molcata.2013.02.022
    日期:2013.6
    The reaction of 3-chloropropyl silica (SilprCl) with 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU) in dry acetone affords silica-bonded 5-n-propyl-octahydro-pyrimido[1,2-a]azepinium chloride (SB-DBU)Cl as a new silica-supported ionic liquid catalyst. Afterward, (SB-DBU)Cl is used for the efficient synthesis of 4H-benzo[b]pyran derivatives via the one-pot, three-component reaction of carbonyl compounds (cyclohexane-1
    3-氯丙基二氧化硅(SilprCl)与1,8-二氮杂双环[5.4.0]十一碳-7-烯(DBU)在干燥的丙酮中的反应得到二氧化硅键合的5-正丙基-八氢-嘧啶基[1,2- a]氯化ze嗪(SB-DBU)Cl作为新型的二氧化硅负载型离子液体催化剂。之后,(SB-DBU)Cl通过羰基化合物(环己烷-1,3-二酮,5,5-一锅法)的三锅法有效合成4 H-苯并[ b ]吡喃衍生物。(1,3-二甲基环己烷-1,3-二酮或3-甲基-1-苯基-2-吡唑啉-5-酮)与芳族醛和烷基丙二酸酯。此外,一些新颖的双(苯并[ b使用(SB-DBU)Cl合成[] pyran] s和在结构上含有羟吲哚和/或喹喔啉部分的多种结构多样的螺-吡喃。将催化剂循环使用十五次,收率不变。
  • Oxalic acid dihydrate: proline as a new recyclable designer solvent: a sustainable, green avenue for the synthesis of spirooxindole
    作者:Dattatray R. Chandam、Abhijeet G. Mulik、Dayanand R. Patil、Madhukar B. Deshmukh
    DOI:10.1007/s11164-015-2093-3
    日期:2016.2
    encouraged to explore oxalic acid dihydrate: proline low transition temperature mixture as a new designer solvent for the said synthesis at room temperature. It has been successfully applied for the three component reaction of isatin, malononitrile or ethyl cyanoacetate and 1,3–dicarbonyl compounds for the first time. Moderate to good yield of the products, shorter reaction time, energy efficiency, chromatography-free
    摘要 为开发具有巨大生物活性的螺氧基吲哚衍生物的环保,可持续协议的要求鼓励了探索草酸二水合物:脯氨酸低转变温度混合物作为在室温下所述合成的新型设计溶剂。它已成功地首次用于靛红,丙二腈或氰基乙酸乙酯与1,3-二羰基化合物的三组分反应。该产品具有中等至良好的收率,较短的反应时间,能源效率,无色谱纯化工艺,可回收性和高原子经济性是该协议的诱人特性,将在多组分,面向多样性的合成中得到应用。 图形概要
  • A New Reaction of Isatin, Cyclic 1,3-Diketone, and 2-Cyanoacetamide: A Four-Component Synthesis of Spirooxindoles
    作者:Ramin Ghahremanzadeh、Ghaffar Hosseini、Roya Akbarzadeh、Ayoob Bazgir
    DOI:10.1002/jhet.1010
    日期:2013.3
    A novel reaction of isatins, 2‐cyanoacetamide, and cyclic 1,3‐diketones in ethanol was reported. The reaction gave the unexpected spirooxindole ethyl carboxylates in excellent yields and the spirooxindole carboxamide was not observed.
    据报道,靛红,2-氰基乙酰胺和环状1,3-二酮在乙醇中发生了新的反应。该反应以优异的产率得到了意想不到的螺并吲哚羧酸乙酯,未观察到螺并吲哚羧酰胺。
  • NaCl as a Novel and Green Catalyst for the Synthesis of Biodynamic Spiro Heterocycles in Water Under Sonication
    作者:Anshu Dandia、Anuj Kumar Jain、Dharmendra Singh Bhati
    DOI:10.1080/00397911.2010.515365
    日期:2011.10
    Abstract An efficient and novel green catalytic protocol for the synthesis of biologically important spirooxindole derivatives is developed in a one-pot, three-component approach involving substituted isatin, activated methylene reagent, and 3-methyl-1-phenyl-2-pyrazolin-5-one in water under sonication. This report describes the use of sodium chloride as a nonacidic and green catalyst for a variety
    摘要 一种用于合成具有生物学意义的螺羟吲哚衍生物的高效、新颖的绿色催化方案是通过一锅、三组分的方法开发的,包括取代的靛红、活化的亚甲基试剂和 3-methyl-1-phenyl-2-pyrazolin-5 - 一个在水中超声处理。本报告描述了氯化钠作为各种底物的非酸性和绿色催化剂的用途。这种方法的优点是环境友好、操作简单、产量高、易于处理以及产品不需要纯化。
  • Step-economic, efficient, ZnS nanoparticle-catalyzed synthesis of spirooxindole derivatives in aqueous medium via Knoevenagel condensation followed by Michael addition
    作者:Anshu Dandia、Vijay Parewa、Anuj Kumar Jain、Kuldeep S. Rathore
    DOI:10.1039/c1gc15244k
    日期:——
    An environmentally friendly, one-pot, three-component ZnS nanoparticle-mediated synthesis of biologically important spirooxindole derivatives in water under ultrasonic irradiation is described herein. ZnS nanoparticles were synthesized by aqueous chemical method. The advantages of this method lies in its simplicity, cost effectiveness, environment friendliness, easier scaling up for large scale synthesis without using high pressure, temperature and toxic chemicals. Greenness of the process was well instituted as water was exploited both as reaction media as well as medium for synthesis of catalyst (ZnS nanoparticles). The particle size was determined by transmission electron microscopy (TEM) and XRD. Compared with other methods for synthesis of spirooxindole derivatives, satisfactory results were obtained with high yields, short reaction time, with simple experimental procedure. After reaction course, the ZnS NPs can be recycled and reused without any apparent loss of activity.
    本文介绍了一种在超声波辐照下,以 ZnS 纳米粒子为介导,在水中合成具有重要生物活性的螺吲哚衍生物的环保型一锅三组份合成方法。ZnS 纳米粒子采用水化学方法合成。这种方法的优点在于简单、成本效益高、环境友好,而且无需使用高压、高温和有毒化学品,更容易进行大规模合成。由于水既可用作反应介质,也可用作合成催化剂(ZnS 纳米粒子)的介质,因此该工艺绿色环保。粒度由透射电子显微镜(TEM)和 XRD 确定。与其他合成螺吲哚衍生物的方法相比,该方法产率高、反应时间短、实验过程简单,取得了令人满意的结果。反应过程结束后,ZnS NPs 可回收再利用,且没有明显的活性损失。
查看更多

同类化合物

(Z)-3-[[[2,4-二甲基-3-(乙氧羰基)吡咯-5-基]亚甲基]吲哚-2--2- (S)-(-)-5'-苄氧基苯基卡维地洛 (R)-(+)-5'-苄氧基卡维地洛 (R)-卡洛芬 (N-(Boc)-2-吲哚基)二甲基硅烷醇钠 (4aS,9bR)-6-溴-2,3,4,4a,5,9b-六氢-1H-吡啶并[4,3-B]吲哚 (3Z)-3-(1H-咪唑-5-基亚甲基)-5-甲氧基-1H-吲哚-2-酮 (3Z)-3-[[[4-(二甲基氨基)苯基]亚甲基]-1H-吲哚-2-酮 (3R)-(-)-3-(1-甲基吲哚-3-基)丁酸甲酯 (3-氯-4,5-二氢-1,2-恶唑-5-基)(1,3-二氧代-1,3-二氢-2H-异吲哚-2-基)乙酸 齐多美辛 鸭脚树叶碱 鸭脚木碱,鸡骨常山碱 鲜麦得新糖 高氯酸1,1’-二(十六烷基)-3,3,3’,3’-四甲基吲哚碳菁 马鲁司特 马来酸阿洛司琼 马来酸替加色罗 顺式-ent-他达拉非 顺式-1,3,4,4a,5,9b-六氢-2H-吡啶并[4,3-b]吲哚-2-甲酸乙酯 顺式-(+-)-3,4-二氢-8-氯-4'-甲基-4-(甲基氨基)-螺(苯并(cd)吲哚-5(1H),2'(5'H)-呋喃)-5'-酮 靛红联二甲酚 靛红磺酸钠 靛红磺酸 靛红乙烯硫代缩酮 靛红-7-甲酸甲酯 靛红-5-磺酸钠 靛红-5-磺酸 靛红-5-硫酸钠盐二水 靛红-5-甲酸甲酯 靛红 靛玉红3'-单肟5-磺酸 靛玉红-3'-单肟 靛玉红 青色素3联己酸染料,钾盐 雷马曲班 雷莫司琼杂质13 雷莫司琼杂质12 雷莫司琼杂质 雷替尼卜定 雄甾-1,4-二烯-3,17-二酮 阿霉素的代谢产物盐酸盐 阿贝卡尔 阿西美辛叔丁基酯 阿西美辛 阿莫曲普坦杂质1 阿莫曲普坦 阿莫曲坦二聚体杂质 阿莫曲坦 阿洛司琼杂质