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6,8-dimethyl-10-phenyl-6,10-dihydro-7H-[1,3]dioxolo[4′,5′:6,7]chromeno[2,3-d]pyrimidine-7,9(8H)-dione | 1309879-39-7

中文名称
——
中文别名
——
英文名称
6,8-dimethyl-10-phenyl-6,10-dihydro-7H-[1,3]dioxolo[4′,5′:6,7]chromeno[2,3-d]pyrimidine-7,9(8H)-dione
英文别名
6,8-dimethyl-10-phenyl-6,10-dihydro-5-oxa-6,8-diazaanthra[2,3-d][1,3]dioxole-7,9-dione;6,8-dimethyl-10-phenyl-6,10-dihydro-7H- [1, 3]dioxolo[4,5:6,7]chromeno[2,3-d]pyrimidine-7,9(8H)-dione;10-phenyl-6,8-dimethyl-6,10-dihydro-5-oxa-6,8-diazaanthra[2,3-d][1,3]dioxole-7,9-dione
6,8-dimethyl-10-phenyl-6,10-dihydro-7H-[1,3]dioxolo[4′,5′:6,7]chromeno[2,3-d]pyrimidine-7,9(8H)-dione化学式
CAS
1309879-39-7
化学式
C20H16N2O5
mdl
——
分子量
364.357
InChiKey
ZSPOPZSJDORTNO-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):
    2.1
  • 重原子数:
    27.0
  • 可旋转键数:
    1.0
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.2
  • 拓扑面积:
    71.69
  • 氢给体数:
    0.0
  • 氢受体数:
    7.0

反应信息

  • 作为产物:
    描述:
    芝麻酚1,3-二甲基巴比妥酸苯甲醛 在 TiO2-SiO2 nanocomposite 作用下, 以 为溶剂, 反应 0.75h, 以95%的产率得到6,8-dimethyl-10-phenyl-6,10-dihydro-7H-[1,3]dioxolo[4′,5′:6,7]chromeno[2,3-d]pyrimidine-7,9(8H)-dione
    参考文献:
    名称:
    TiO2-SiO2纳米复合材料在水介质中快速高效合成色基[d]嘧啶二酮
    摘要:
    1:1 TiO2-SiO2 纳米复合材料被用作一种高效且绿色可回收的催化剂,用于在水中合成 11 种色基[d]嘧啶二酮,其中 6 种是新的。所有反应均在非常温和的条件下进行,以优异的产率得到相应的产物。
    DOI:
    10.3184/174751917x14949407124706
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文献信息

  • Synthesis and in vitro evaluation of antioxidant activity of diverse naphthopyranopyrimidines, diazaanthra[2,3-d][1,3]dioxole-7,9-dione and tetrahydrobenzo[a]xanthen-11-ones
    作者:Jitender M. Khurana、Anshika Lumb、Ankita Chaudhary、Bhaskara Nand
    DOI:10.1039/c2ra22406b
    日期:——
    A green and efficient one pot three component protocol has been developed for the synthesis of naphthopyranopyrimidines, diazaanthra[2,3-d][1,3]dioxole-7,9-dione and tetrahydrobenzo[a]xanthen-11-ones in PEG-400 catalyzed by alum (KAl(SO4)2·12H2O). Single crystal X-ray diffraction studies have been performed for naphthopyranopyrimidine (5). The synthesized compounds were screened for in vitro antioxidant activity by DPPH scavenging assay and compounds 3 and 4 manifested profound antioxidant potential.
    明矾(KAl(SO4)2-12H2O)的催化下,开发了一种在 PEG-400 中合成嘧啶、二氮杂并[2,3-d][1,3]二恶茂-7,9-二酮和四氢苯并[a]氧杂蒽-11-酮的绿色高效的一锅三组分方案。对嘧啶 (5) 进行了单晶 X 射线衍射研究。通过 DPPH 清除试验对合成的化合物进行了体外抗氧化活性筛选,结果表明化合物 3 和 4 具有很强的抗氧化潜力。
  • Activated Carbon/MoO3: Efficient Catalyst for Green Synthesis of Chromeno[d]pyrimidinediones and Xanthenones
    作者:Niloofar Sabet Mehr、Shahrzad Abdolmohammadi、Maryam Afsharpour
    DOI:10.2174/1386207323666200924111602
    日期:2021.6
    organic reactions because they have been found to influence the chemical and physical properties of bulk material. The chromene (benzopyran) nucleus constitutes the core structure in a major class of many biologically active compounds, and interest in their chemistry consequently continues because of their numerous biological activities. The xanthene (dibenzopyran) derivatives are classified as highly significant
    背景:纳米级金属氧化物催化剂已被广泛用于有机反应,因为已发现它们会影响散装材料的化学和物理性质。色烯(苯并喃)核构成了许多生物活性化合物的主要类别的核心结构,由于其众多的生物活性,因此对其化学的兴趣继续存在。呫吨(二苯并喃)衍生物被归类为具有多种生物活性特性的非常重要的化合物。嘧啶酮还因其显着的生物利用而引起了人们的兴趣,例如抗病毒、抗菌、抗高血压、抗肿瘤和阻滞剂作用。 目的:本文提出的这项工作的目的是制备活性炭/MoO3 纳米复合材料,并探索其作为绿色和可回收催化剂的作用,用于在室温下乙醇滴磨下合成色基[d]嘧啶二酮和呫吨酮。 方法:以树胶的碳化为新的天然前驱体合成活性炭,通过简单的途径成功制备了活性炭/MoO3纳米复合材料。然后,该纳米复合材料有效地用于 3,4-亚甲基二氧基苯酚、芳香醛和活性亚甲基化合物(包括 1,3-二甲基巴比妥酸二甲酮)的反应,以高产率合成一系列色诺[d]
  • Zr(HSO4)4 as an efficient catalyst for the preparation of 10-aryl-6,8-dimethyl-6,10dihydro-5-oxa-6,8-diazaanthra[2,3-d][1,3]dioxole-7,9-diones under solvent-free conditions
    作者:Jiangli Zhang、Wei Lin Li、Li Qiang Wu
    DOI:10.1590/s0103-50532011000700006
    日期:——
    A one-pot three-component condensation of 3,4-methylenedioxyphenol, aromatic aldehydes, and 1,3-dimethylbarbituric acid, efficiently promoted in the presence of Zr(HSO4)4 under solvent-free conditions, produced 10-aryl-6,8-dimethyl-6,10-dihydro-5-oxa-6,8-diazaanthra[2,3-d][1,3] dioxole-7,9-diones. The method offers several advantages including simple, easy and clean work-up procedure, relatively short reaction times and good to high yields of the products.
    在 Zr(HSO4)4 存在下,在无溶剂条件下,3,4-亚甲基二氧基苯酚、芳香醛和 1,3-二甲基巴比妥酸的一锅三组分缩合得到有效促进,生成 10-芳基-6, 8-二甲基-6,10-二氢-5-氧杂-6,8-二氮杂[2,3-d][1,3]二氧杂环戊烯-7,9-二酮。该方法具有多种优点,包括简单、容易和清洁的后处理程序、相对较短的反应时间以及良好至高的产物收率。
  • Melamine Trisulfonic Acid: An Efficient, Heterogeneous and Reusable Catalyst for the Synthesis of 10-Aryl-6,8-dimethyl- 6, 10-dihydro-5-oxa-6,8-diazaanthra [2,3-d][1,3]dioxole- 7,9-diones
    作者:Weilin Li、Qiuyan Luo
    DOI:10.1155/2011/853747
    日期:——

    Melamine trisulfonic acid was used as an efficient and recyclable catalyst for the one-pot synthesis of 10-aryl-6,8-dimethyl-6,10-dihydro-5-oxa-6,8-diazaanthra[2,3-d][1,3]dioxole-7,9-diones by condensation of 3,4-methylene dioxyphenol, aromatic aldehydes and 1,3-dimethylbarbituric acid under solvent-free conditions. Different types of aromatic. aldehydes were used in the reaction and in all cases the products were obtained in good to excellent yields.

    磺酸三聚氰胺被用作高效可循环催化剂,用于在无溶剂条件下通过3,4-亚甲二氧苯酚、芳香醛和1,3-二甲基巴比妥酸的缩合反应合成10-芳基-6,8-二甲基-6,10-二氢-5-氧-6,8-二氮杂[2,3-d][1,3]二噁烷-7,9-二酮。反应中使用了不同类型的芳香醛,在所有情况下产物的收率都在良好至优秀之间。
  • Cyanuric chloride-catalyzed synthesis of 10-aryl-6,8-dimethyl-6,10-dihydro-5-oxa-6,8-diazaanthra[2,3-d][1,3]dioxole-7,9-diones
    作者:Wei Lin Li、Qiu Yan Luo、Fu Lin Yan
    DOI:10.1016/j.cclet.2011.01.020
    日期:2011.7
    An environmentally friendly procedure for the preparation of 10-aryl-6,8-dimethyl-6,10-dihydro-5-oxa-6,8-diazaanthra[2,3-d][1,3]dioxole-7,9-diones under thermal solvent-free conditions in the presence of cyanuric chloride as heterogeneous catalyst was developed. (C) 2011 Wei Lin Li. Published by Elsevier B.V. on behalf of Chinese Chemical Society. All rights reserved.
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同类化合物

()-2-(5-甲基-2-氧代苯并呋喃-3(2)-亚乙基)乙酸乙酯 (双(2,2,2-三氯乙基)) (乙基N-(1H-吲唑-3-基羰基)ethanehydrazonoate) (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 (S)-(-)-2-(α-(叔丁基)甲胺)-1H-苯并咪唑 (S)-(-)-2-(α-甲基甲胺)-1H-苯并咪唑 (S)-氨氯地平-d4 (S)-8-氟苯并二氢吡喃-4-胺 (S)-4-(叔丁基)-2-(喹啉-2-基)-4,5-二氢噁唑 (S)-4-氯-1,2-环氧丁烷 (S)-3-(2-(二氟甲基)吡啶-4-基)-7-氟-3-(3-(嘧啶-5-基)苯基)-3H-异吲哚-1-胺 (S)-2-(环丁基氨基)-N-(3-(3,4-二氢异喹啉-2(1H)-基)-2-羟丙基)异烟酰胺 (SP-4-1)-二氯双(喹啉)-钯 (SP-4-1)-二氯双(1-苯基-1H-咪唑-κN3)-钯 (R,S)-可替宁N-氧化物-甲基-d3 (R,S)-六氢-3H-1,2,3-苯并噻唑-2,2-二氧化物-3-羧酸叔丁酯 (R)-(+)-5'-苄氧基卡维地洛 (R)-(+)-2,2'',6,6''-四甲氧基-4,4''-双(二苯基膦基)-3,3''-联吡啶(1,5-环辛二烯)铑(I)四氟硼酸盐 (R)-卡洛芬 (R)-N'-亚硝基尼古丁 (R)-DRF053二盐酸盐 (R)-4-异丙基-2-恶唑烷硫酮 (R)-3-甲基哌啶盐酸盐; (R)-2-苄基哌啶-1-羧酸叔丁酯 (N-(Boc)-2-吲哚基)二甲基硅烷醇钠 (N-{4-[(6-溴-2-氧代-1,3-苯并恶唑-3(2H)-基)磺酰基]苯基}乙酰胺) (E)-2-氰基-3-(5-(2-辛基-7-(4-(对甲苯基)-1,2,3,3a,4,8b-六氢环戊[b]吲哚-7-基)-2H-苯并[d][1,2,3]三唑-4-基)噻吩-2-基)丙烯酸 (E)-2-氰基-3-[5-(2,5-二氯苯基)呋喃-2-基]-N-喹啉-8-基丙-2-烯酰胺 (8α,9S)-(+)-9-氨基-七氢呋喃-6''-醇,值90% (6R,7R)-7-苯基乙酰胺基-3-[(Z)-2-(4-甲基噻唑-5-基)乙烯基]-3-头孢唑啉-4-羧酸二苯甲基酯 (6-羟基嘧啶-4-基)乙酸 (6,7-二甲氧基-4-(3,4,5-三甲氧基苯基)喹啉) (6,6-二甲基-3-(甲硫基)-1,6-二氢-1,2,4-三嗪-5(2H)-硫酮) (5aS,6R,9S,9aR)-5a,6,7,8,9,9a-六氢-6,11,11-三甲基-2-(2,3,4,5,6-五氟苯基)-6,9-甲基-4H-[1,2,4]三唑[3,4-c][1,4]苯并恶嗪四氟硼酸酯 (5R,Z)-3-(羟基((1R,2S,6S,8aS)-1,3,6-三甲基-2-((E)-prop-1-en-1-yl)-1,2,4a,5,6,7,8,8a-八氢萘-1-基)亚甲基)-5-(羟甲基)-1-甲基吡咯烷-2,4-二酮 (5E)-5-[(2,5-二甲基-1-吡啶-3-基-吡咯-3-基)亚甲基]-2-亚磺酰基-1,3-噻唑烷-4-酮 (5-(4-乙氧基-3-甲基苄基)-1,3-苯并二恶茂) (5-溴-3-吡啶基)[4-(1-吡咯烷基)-1-哌啶基]甲酮 (5-氯-2,1,3-苯并噻二唑-4-基)-氨基甲氨基硫代甲酸甲酯一氢碘 (5-氨基-6-氰基-7-甲基[1,2]噻唑并[4,5-b]吡啶-3-甲酰胺) (5-氨基-1,3,4-噻二唑-2-基)甲醇 (4aS-反式)-八氢-1H-吡咯并[3,4-b]吡啶 (4aS,9bR)-6-溴-2,3,4,4a,5,9b-六氢-1H-吡啶并[4,3-B]吲哚 (4S,4''S)-2,2''-环亚丙基双[4-叔丁基-4,5-二氢恶唑] (4-(4-氯苯基)硫代)-10-甲基-7H-benzimidazo(2,1-A)奔驰(德)isoquinolin-7一 (4-苄基-2-甲基-4-nitrodecahydropyrido〔1,2-a][1,4]二氮杂) (4-甲基环戊-1-烯-1-基)(吗啉-4-基)甲酮 (4-己基-2-甲基-4-nitrodecahydropyrido〔1,2-a][1,4]二氮杂) (4,5-二甲氧基-1,2,3,6-四氢哒嗪)