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7-amino-4-oxo-2-thioxo-5-(3,4,5-trimethoxyphenyl)-2,3,4,5-tetrahydro-1H-pyrano[2,3-d]pyrimidine-6-carbonitrile | 1357001-36-5

中文名称
——
中文别名
——
英文名称
7-amino-4-oxo-2-thioxo-5-(3,4,5-trimethoxyphenyl)-2,3,4,5-tetrahydro-1H-pyrano[2,3-d]pyrimidine-6-carbonitrile
英文别名
7-Amino-4-oxo-2-thioxo-5-(3,4,5-trimethoxyphenyl)-1,5-dihydropyrano[2,3-d]pyrimidine-6-carbonitrile;7-amino-4-oxo-2-sulfanylidene-5-(3,4,5-trimethoxyphenyl)-1,5-dihydropyrano[2,3-d]pyrimidine-6-carbonitrile
7-amino-4-oxo-2-thioxo-5-(3,4,5-trimethoxyphenyl)-2,3,4,5-tetrahydro-1H-pyrano[2,3-d]pyrimidine-6-carbonitrile化学式
CAS
1357001-36-5
化学式
C17H16N4O5S
mdl
——
分子量
388.404
InChiKey
CLMMUBHUKIUGLW-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):
    1.1
  • 重原子数:
    27
  • 可旋转键数:
    4
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.24
  • 拓扑面积:
    160
  • 氢给体数:
    3
  • 氢受体数:
    8

上下游信息

  • 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:
    甲酸7-amino-4-oxo-2-thioxo-5-(3,4,5-trimethoxyphenyl)-2,3,4,5-tetrahydro-1H-pyrano[2,3-d]pyrimidine-6-carbonitrile 反应 12.0h, 以73%的产率得到13-Sulfanylidene-9-(3,4,5-trimethoxyphenyl)-2-oxa-4,6,12,14-tetrazatricyclo[8.4.0.03,8]tetradeca-1(10),3(8),4-triene-7,11-dione
    参考文献:
    名称:
    新型稠合铬诺[2,3- d ]嘧啶和吡喃并[2,3- d ]嘧啶衍生物的高效一锅制备
    摘要:
    已经合成了一些新颖的铬诺[2,3- d ]嘧啶酮,吡喃并[2,3- d ]嘧啶,二氢嘧啶,吡啶并吡喃并嘧啶和嘧啶并吡喃并嘧啶。通过元素分析和光谱数据确认了目标化合物的结构。测试了所有目标合成化合物对各种微生物如铜绿假单胞菌(Pseudomonas aeruginosa)的抗菌活性; 金黄色葡萄球菌(细菌),黄曲霉(真菌)和白色念珠菌(酵母菌​​)采用圆盘扩散法。通常,新合成的化合物对前面提到的微生物显示出良好的抗菌活性。
    DOI:
    10.1016/j.ejmech.2011.09.040
  • 作为产物:
    描述:
    4,6-二羟基-2-巯基嘧啶[(3,4,5-三甲氧基苯基)亚甲基]丙二腈三乙胺 作用下, 以 乙醇 为溶剂, 反应 3.0h, 以85%的产率得到7-amino-4-oxo-2-thioxo-5-(3,4,5-trimethoxyphenyl)-2,3,4,5-tetrahydro-1H-pyrano[2,3-d]pyrimidine-6-carbonitrile
    参考文献:
    名称:
    新型稠合铬诺[2,3- d ]嘧啶和吡喃并[2,3- d ]嘧啶衍生物的高效一锅制备
    摘要:
    已经合成了一些新颖的铬诺[2,3- d ]嘧啶酮,吡喃并[2,3- d ]嘧啶,二氢嘧啶,吡啶并吡喃并嘧啶和嘧啶并吡喃并嘧啶。通过元素分析和光谱数据确认了目标化合物的结构。测试了所有目标合成化合物对各种微生物如铜绿假单胞菌(Pseudomonas aeruginosa)的抗菌活性; 金黄色葡萄球菌(细菌),黄曲霉(真菌)和白色念珠菌(酵母菌​​)采用圆盘扩散法。通常,新合成的化合物对前面提到的微生物显示出良好的抗菌活性。
    DOI:
    10.1016/j.ejmech.2011.09.040
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文献信息

  • Nio Nanoparticles: A Highly Efficient Catalyst for the One-Pot Three- Component Synthesis of Pyrano [2, 3-D] Pyrimidine Derivatives in Green Reaction Media
    作者:Ellahe Sabbaghnasab、Enayatollah Sheikhhosseini
    DOI:10.2174/1570178618666211001115655
    日期:2022.7
    Abstract:

    NiO nanoparticles are utilized to effectively strengthen annulated pyrano [2,3-d] pyrimidine synthesis through primary Knoevenagel, following Micheal and ultimate heterocyclization reactions of aldehyde, malononitrile, and barbituric acid. The characteristics of NiO nanoparticles are identified using advanced techniques, such as IR, UV, EDX, XRD, SEM, and TEM. The nano-NiO particles are mostly below < 100 nm in size with uniform spherical shapes. The adopted approach is advantages owing to its simple processing, relatively short reaction time, often good to high average yields, convenient workability, and environmental friendliness.

    摘要:使用NiO纳米颗粒有效地强化了环戊基吡喃[2,3-d]嘧啶的合成,通过首要的Knoevenagel,随后的Michael和最终的醛,马隆酸腈和巴比妥酸的杂环化反应。采用先进的技术,如IR,UV,EDX,XRD,SEM和TEM,确定了NiO纳米颗粒的特性。纳米NiO颗粒的大小大多数在<100纳米,呈均一的球形。采用的方法具有简单的处理、相对较短的反应时间、常常具有良好的到高收率、方便的可操作性和环境友好性的优点。
  • Efficient one-pot preparation of novel fused chromeno[2,3-d]pyrimidine and pyrano[2,3-d]pyrimidine derivatives
    作者:Hala M. Aly、Mona M. Kamal
    DOI:10.1016/j.ejmech.2011.09.040
    日期:2012.1
    Some novel chromeno[2,3-d]pyrimidinone, pyrano[2,3-d]pyrimidine, dihydropyrimidine, pyridopyranopyrimidine and pyrimidopyranopyrimidine have been synthesized. The structures of target compounds were confirmed by elemental analyses and spectral data. The antimicrobial activity of all the target synthesized compounds were tested against various microorganismst such as Pseudomonas aeruginosa; Staphylococcus
    已经合成了一些新颖的铬诺[2,3- d ]嘧啶酮,吡喃并[2,3- d ]嘧啶,二氢嘧啶,吡啶并吡喃并嘧啶和嘧啶并吡喃并嘧啶。通过元素分析和光谱数据确认了目标化合物的结构。测试了所有目标合成化合物对各种微生物如铜绿假单胞菌(Pseudomonas aeruginosa)的抗菌活性; 金黄色葡萄球菌(细菌),黄曲霉(真菌)和白色念珠菌(酵母菌​​)采用圆盘扩散法。通常,新合成的化合物对前面提到的微生物显示出良好的抗菌活性。
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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