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7'-amino-1,2'-dimethyl-5-nitro-2,4'-dioxo-3',4'-dihydrospiro[indoline-3,5'-pyrano[2,3-d]pyrimidine]-6'-carbonitrile | 1204748-08-2

中文名称
——
中文别名
——
英文名称
7'-amino-1,2'-dimethyl-5-nitro-2,4'-dioxo-3',4'-dihydrospiro[indoline-3,5'-pyrano[2,3-d]pyrimidine]-6'-carbonitrile
英文别名
7'-amino-4'-hydroxy-1,2'-dimethyl-5-nitro-2-oxospiro[indoline-3,5'-pyrano[2,3-d]pyrimidine]-6'-carbonitrile;7-amino-1',2-dimethyl-5'-nitro-2',4-dioxospiro[3H-pyrano[2,3-d]pyrimidine-5,3'-indole]-6-carbonitrile
7'-amino-1,2'-dimethyl-5-nitro-2,4'-dioxo-3',4'-dihydrospiro[indoline-3,5'-pyrano[2,3-d]pyrimidine]-6'-carbonitrile化学式
CAS
1204748-08-2
化学式
C17H12N6O5
mdl
——
分子量
380.319
InChiKey
NFYJQNSYFCSJOZ-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

计算性质

  • 辛醇/水分配系数(LogP):
    -0.5
  • 重原子数:
    28
  • 可旋转键数:
    0
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.18
  • 拓扑面积:
    167
  • 氢给体数:
    2
  • 氢受体数:
    8

反应信息

  • 作为产物:
    描述:
    1-甲基-5-硝基靛红2-甲基-4,6-二羟基嘧啶丙二腈 在 copper(II) ferrite 作用下, 以 为溶剂, 反应 0.5h, 以81%的产率得到7'-amino-1,2'-dimethyl-5-nitro-2,4'-dioxo-3',4'-dihydrospiro[indoline-3,5'-pyrano[2,3-d]pyrimidine]-6'-carbonitrile
    参考文献:
    名称:
    铜铁氧体纳米粒子:一种高效和可重复使用的纳米催化剂,用于水中的螺一氧化三吲哚的绿色单罐,三组分合成
    摘要:
    据报道,通过使用可磁回收和可重复使用的催化剂,靛红,活性氰基甲烷和环状1,3-二羰基衍生物在回流水中进行高效,简单的一锅三组分合成螺环吲哚稠合杂环的绿色反应。该方法的特点是,使用可磁回收和可重复使用的催化剂,温和的反应条件,高至优异的产品收率,操作简便和后处理程序容易。最重要的是,催化剂容易的磁分离消除了反应完成后对催化剂过滤的需要。此外,即使重复使用5次,催化剂也保持高活性。
    DOI:
    10.1021/co400057h
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文献信息

  • An efficient, three-component synthesis of spiro[benzo[<i>g</i>]chromene-4,3′-indoline]-3-carbonitrile and spiro[indoline-3,5′-pyrano[2,3-<i>d</i>]pyrimidine]-6′-carbonitrile derivatives
    作者:Ramin Ghahremanzadeh、Tayebeh Amanpour、Ayoob Bazgir
    DOI:10.1002/jhet.240
    日期:2009.11
    Abstract magnified image Spiro[benzo[g]chromene‐4,3′‐indoline]‐3‐carbonitriles and spiro[indoline‐3,5′‐pyrano[2,3‐d]pyrimidine]‐6′‐carbonitriles were synthesized via a three‐component reaction of isatins, 2‐hydroxynaphthalene‐1,4‐dione or 2‐methylpyrimidine‐4,6‐diol, and malononitrile in aqueous media. J. Heterocyclic Chem., (2009).
  • One-pot and three-component synthesis of spiro[chromeno[2,3-d] pyrimidine-5,3′-indoline]-diones and spiro[chromeno[2,3-c] pyrazole-4,3′-indoline]-diones
    作者:Ramin Ghahremanzadeh、Fatemeh Fereshtehnejad、Zahra Yasaei、Tayebeh Amanpour、Ayoob Bazgir
    DOI:10.1002/jhet.399
    日期:——
    Abstract magnified image A novel, clean, one‐pot and three‐component synthesis of new spiro[chromeno[2,3‐d]pyrimidine‐5,3′‐indoline]‐2′,6(7H)‐diones and spiro[chromeno[2,3‐c]pyrazole‐4,3′‐indoline]‐2′,5(6H)‐diones via cyclo‐condensation reaction of isatins, 1,3‐cyclohexadiones, and 2‐methylpyrimidine‐4,6‐diol or 3‐methyl‐1‐phenyl‐1H‐pyrazol‐5‐ol, in aqueous media is reported. J. Heterocyclic Chem., (2010).
  • Copper Ferrite Nanoparticles: An Efficient and Reusable Nanocatalyst for a Green One-Pot, Three-component Synthesis of Spirooxindoles in Water
    作者:Ayoob Bazgir、Ghaffar Hosseini、Ramin Ghahremanzadeh
    DOI:10.1021/co400057h
    日期:2013.10.14
    A green reaction of isatins, active cyanomethanes, and cyclic 1,3-dicarbonyl derivatives for the efficient and simple one-pot three-component synthesis of spirooxindole fused heterocycles in refluxing water by use of magnetically recoverable and reusable catalyst is reported. The features of this procedure are, the use of magnetically recoverable and reusable catalyst, mild reaction conditions, high
    据报道,通过使用可磁回收和可重复使用的催化剂,靛红,活性氰基甲烷和环状1,3-二羰基衍生物在回流水中进行高效,简单的一锅三组分合成螺环吲哚稠合杂环的绿色反应。该方法的特点是,使用可磁回收和可重复使用的催化剂,温和的反应条件,高至优异的产品收率,操作简便和后处理程序容易。最重要的是,催化剂容易的磁分离消除了反应完成后对催化剂过滤的需要。此外,即使重复使用5次,催化剂也保持高活性。
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同类化合物

乙基7'-氨基-6-氟-2,2',4'-三羰基-1,1',2,2',3',4'-六氢螺[吲哚-3,5'-吡喃并[2,3-d]嘧啶]-6'-羧酸酯 7H-吡喃并[2,3-d]嘧啶-7-酮 7H-吡喃并[2,3-d]嘧啶 7,8-二氢-5H-吡喃并[4,3-D]嘧啶-2-胺 5H-吡喃并[4,3-d]嘧啶 5H-吡喃并[2,3-d]嘧啶 2H-吡喃并[2,3-d]嘧啶-6-甲腈,7-氨基-1,3,4,5-四氢-5-(4-甲氧苯基)-2,4-二羰基- 2,4-二氯-7,8-二氢-5H-吡喃[4,3-d]嘧啶 1H-吡喃并[3,4-d]嘧啶 1H-吡喃并[3,2-d]嘧啶 4-(4-methoxyaniline)-5-(phenyl)-8,9-dihydro-5H-chromeno[2,3-d]pyrimidin-6(7H)-one 4-cyclohexyl-2-phenyl-7,8-dihydro-6H-pyranol[3,2-d]pyrimidine 1,3-Bis(p-tolyl)-5-(2'-hydroxyphenyl)-7-methyl-4-oxo-1,2,3,4-tetrahydro-2-thioxo-5H-pyrano<2,3-d>pyrimidine 7,8-dihydro-3H-pyrano[4,3-d]pyrimidin-4(5H)-one 7-amino-2,3,4,5-tetrahydro-5-(3-hydroxyphenyl)-1,3-dimethyl-2,4-dioxo-1H-pyrano[2,3-d]pyrimidine-6-carbonitrile 3-benzyl-6,6,9-trimethyl-6a,7,8,9,10,10a-hexahydro-6H-isochromeno[3,4-d]pyrimidin-1-ol 7'-amino-1-ethyl-2,4'-dioxo-2'-thioxo-1',2',3',4'-tetrahydrospiro[indoline-3,5'-pyrano[2,3-d] pyrimidine]-6'-carbonitrile 7'-amino-2,4'-dioxo-2'-thioxo-1',2',3',4'-tetrahydro-2H-spiro[acenaphthylene-1,5'-pyrano[2,3-d]pyrimidine]-6'-carbonitrile (3-(((2-(4-(but-2-ynamido)-2-methyl-1H-indol-1-yl)-7,8-dihydro-5H-pyrano[4,3-d]pyrimidin-4-yl)amino)methyl)phenyl)boronic acid 7-amino-5-(2,3-dimethoxyphenyl)-1,3-dimethyl-2,4-dioxo-2,3,4,5-tetrahydro-1H-pyrano[2,3-d]pyrimidine-6-carbonitrile 7'-amino-5-chloro-1',3'-dimethyl-2,2',4'-trioxo-1',2',3',4'-tetrahydrospiro[indoline-3,5'-pyrano[2,3-d]pyrimidine]-6'-carbonitrile 7-amino-5-(4-bromophenyl)-1,3-dimethyl-2,4-dioxo-1,3,4,5-tetrahydro-2H-pyrano[2,3-d]pyrimidine-6-carbonitrile 7-amino-5-(4-methoxyphenyl)-1,3-dimethyl-2,4-dioxo-1,3,4,5-tetrahydro-2H-pyrano[2,3-d]-pyrimidine-6-carbonitrile 7,8-dihydro-5H-pyrano[4,3-d]pyrimidine ethyl 2,8-dimethyl-10-phenyl-10H-pyrano[3,2-e][1,2,4]triazolo[1,5-c] pyrimidine-9-carboxylate ethyl 10-(4-methoxyphenyl)-2,8-dimethyl-10H-pyrano[3,2-e][1,2,4]triazolo[1,5-c] pyrimidine-9-carboxylate ethyl 3-{[3-(4-methoxyphenyl)isoxazol-5-yl]methyl}-2,7-dimethyl-4-oxo-5-(p-tolyl)-3,5-dihydro-4H-pyrano[2,3-d]pyrimidine-6-carboxylate 2-thioxo-2,3,7,8-tetrahydro-1H-pyrano[4.3-d]pyrimidin-4(5H)-one 7-amino-2,4-dioxo-5-(m-tolyl)-1,3,4,5-tetrahydro-2H-pyrano[2,3-d]pyrimidine-6-carbonitrile Ethyl 7-amino-5-(4-hydroxyphenyl)-2,4-dioxo-2,3,4,5-tetrahydro-1H-pyrano[2,3-d]pyrimidine-6-carboxylate 7-amino-5-(3-chlorophenyl)-2,4-dioxo-2,3,4,5-tetrahydro-1H-pyrano[2,3-d]pyrimidine-6-carbonitrile 7-amino-5-(2,4-di-chlorophenyl)-2,4-dioxo-2,3,4,5-tetrahydro-1H-pyrano[2,3-d]pyrimidine-6-carbonitrile 7-amino-5-(4-(dimethylamino)phenyl)-2,4-dioxo-2,3,4,5-tetrahydro-1H-pyrano[2,3-d]pyrimidine-6-carbonitrile Ethyl 7-amino-5-(3,4-dimethoxyphenyl)-2,4-dioxo-1,3,4,5-tetrahydro-2H-pyrano[2,3-d]pyrimidine-6-carboxylate 7-amino-5-(3,4-dimethoxyphenyl)-2,4-dioxo-2,3,4,5-tetrahydro-1H-pyrano[2,3-d]pyrimidine-6-carbonitrile ethyl-7-amino-5-(3-nitrphenyl)-2,4-dioxo-2,3,4,5-tetrahydro-1H-pyrano[2,3-d]pyrimidine-6-carboxylate Ethyl 7-amino-5-(4-nitrophenyl)-2,4-dioxo-1,3,4,5-tetrahydro-2H-pyrano[2,3-d]pyrimidine-6-carboxylate Ethyl 7-amino-5-(4-methylphenyl)-2,4-dioxo-1,3,4,5-tetrahydro-2H-pyrano[2,3-d]pyrimidine-6-carboxylate 7'-amino-5-chloro-2,2',4'-trioxo-1',2',3',4'-tetrahydrospiro[indoline-3,5'-pyrano[2,3-d]pyrimidine]-6'-carbonitrile 4-tert-butyl-2-phenyl-7,8-dihydro-6H-pyranol[3,2-d]pyrimidine 6-benzamido-2,3-dihydro-5-methyl-1,3-di(p-chlorophenyl)-2-thioxo-4H-pyrano[2,3-d]pyrimidine-4,7(1H)-dione 6-benzamido-2,3-dihydro-5-methyl-1,3-diphenyl-2-thioxo-4H-pyrano[2,3-d]pyrimidine-4,7(1H)-dione 4-phenylhexahydro-1H-pyrano[2,3-d]pyrimidin-2(8aH)-one 4-(4-methoxyphenyl)hexahydro-1H-pyrano[2,3-d]pyrimidin-2(8aH)-one 7-amino-1,3-dimethyl-2,4-dioxo-5-phenyl-1,3,4,5-tetrahydro-2H-pyrano[2,3-d]pyrimidine-6-carbonitrile 7'‑amino‑2,4′‑dioxo‑2′‑thioxo‑1′,2′,3′,4′‑tetrahydrospiro[indoline‑3,5'‑pyrano[2,3‑d]pyrimidine]‑6'‑carbonitrile 7-Amino-5-(1H-indol-3-yl)-2,4-dioxo-2,3,4,5-tetrahydro-1H-pyrano[2,3-d] pyrimidine-6-carbonitrile methyl 2-amino-5,7-dioxospiro[1'-methyl-3'H-indol-3',4-4H-5,6,7,8-tetrahydropyrano[2,3-d]pyramidine]-1'H-2'-one-3-carboxylate 7-benzyl-7-methyl-4-phenyl-3,4,7,8-tetrahydro-1H-pyrano[4,3-d]pyrimidine-2,5-dione 7,7-dimethyl-4-phenyl-2-thioxo-1,2,3,4,7,8-hexahydro-pyrano[4,3-d]pyrimidin-5-one