1-(2,4-二氯苯基)-3-苯基-1-丙酮 | 898788-78-8

• 分子结构分类: 有机化合物 - 苯丙烷和聚酮 - 直链 1,3-二芳基丙烷
• 中文名称: 1-(2,4-二氯苯基)-3-苯基-1-丙酮
• 英文名称: 1-(2,4-dichlorophenyl)-3-phenylpropan-1-one
• CAS: 898788-78-8
• 化学式: C₁₅H₁₂Cl₂O
• mdl: MFCD03842950
• 分子量: 279.166
• InChiKey: CHKGJRDHLQYPKB-UHFFFAOYSA-N

物化性质

• 沸点：
  401.3±35.0 °C(Predicted)
• 密度：
  1.257±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  4.8
• 重原子数：
  18
• 可旋转键数：
  4
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.133
• 拓扑面积：
  17.1
• 氢给体数：
  0
• 氢受体数：
  1

安全信息

• 海关编码：
  2914700090

反应信息

• 作为反应物：
  描述：

  1-(2,4-二氯苯基)-3-苯基-1-丙酮 在 aluminum (III) chloride 、 溴 、 sodium acetate 作用下， 以 乙醇 、 氯仿 为溶剂， 反应 6.0h， 生成 5-benzyl-4-(2,4-dichlorophenyl)thiazol-2-amine
  参考文献：
  名称：

  2,4,5-Trisubstituted thiazole derivatives: A novel and potent class of non-nucleoside inhibitors of wild type and mutant HIV-1 reverse transcriptase

  摘要：

  Novel 2,4,5-trisubstituted thiazole derivatives (TSTs) were designed and synthesized as HIV-1 non-nucleoside reverse transcriptase inhibitors (NNRTIs). Among the thirty-eight synthesized target compounds, thirty TSTs showed potent inhibition against HIV-1 replication in wild type HIV-1 at submicromolar concentrations (from 0.046 to 9.59 mu M). Compounds 21, 23 and 24 were also tested on seven NNRTI-resistant HIV-1 strains, and all exhibited inhibitory effects with fold changes in IC50 ranging from 2.6 to 111, which were better than those of nevirapine (15.6-fold-371-fold). Docking simulations of compound 24 revealed a reasonable mechanism for the binding mode, and three-dimensional quantitative structure activity relationship (3-DQSAR) studies on this novel series of TST further elucidated the structure-activity relationship (SAR). The results suggested the great potential of TSTs as a novel class of NNRTIs with antiviral efficacy and a good resistance profile. (C) 2014 Elsevier Masson SAS. All rights reserved.

  DOI：

  10.1016/j.ejmech.2014.07.072
• 作为产物：
  描述：

  2,4-二氯苯乙酮 在 偶氮二异丁腈 、 三正丁基氢锡 、 potassium hydroxide 作用下， 以 乙醇 、 苯 为溶剂， 反应 7.0h， 生成 1-(2,4-二氯苯基)-3-苯基-1-丙酮
  参考文献：
  名称：

  通过自由基介导的分子内环化有效合成 3-Aryl-5-chloroindan-1-ones

  摘要：

  摘要 一种有效的自由基介导的分子内环化策略已被开发用于合成 3-aryl-5-chloroindan-1-ones。在自由基条件下分子内环化后，不同取代的 2,4-二氯烯酮以定量产率提供 3-芳基-5-氯茚满-1-酮。图形概要

  DOI：

  10.1080/00397911.2013.813053

文献信息

• Synthesis and oral antifungal activity of novel azolylpropanolones and related compounds
  作者：Masaru Ogata、Hiroshi Matsumoto、Kimio Takahashi、Sumio Shimizu、Shiro Kida、Akira Murabayashi、Motoo Shiro、Katsuya Tawara

  DOI：10.1021/jm00389a016

  日期：1987.6

  their antifungal activities in vitro by evaluation of broth dilution MIC values against three species of fungi and the inhibitory effect on pseudomycelium of Candida albicans, and they were examined for oral efficacy in vivo against subacute systemic candidiasis in mice and superficial dermatophytosis in guinea pigs. Compounds 2, 12, 38, 39, and 92 exhibited strong oral antifungal activity. An asymmetric

  为了找到口服活性抗真菌剂，合成了新的咪唑基-和1,2,4-三唑基丙醇酮I和相关化合物II-IV。化合物I衍生自酮V（方法A），α-二酮IX（方法B），α-羟基酮X（方法C），α-氯酮XII（方法D）和烯酮VI（方法E）。使用N，N'-羰基二咪唑，亚硫酰氯，N，N'-（硫代羰基）二咪唑，溴氯甲烷，2,2-二甲氧基丙烷和环己酮将由I与NaBH4合成的二元醇II环化为五元环状化合物III。二甲基缩酮。通过Grignard反应（方法F），X的羟甲基化（方法G）和酮XXI与1-[（（三甲基甲硅烷基）甲基] -1，2，4-三唑（方法H）的反应，由I合成二元醇IV。通过评价肉汤对三种真菌的稀释MIC值和对白色念珠菌假菌丝体的抑制作用，检查了化合物I-IV的体外抗真菌活性，并在小鼠和小鼠体内检查了它们对亚急性系统性念珠菌病的口服药效。豚鼠浅表皮肤癣菌病。化合物2、12、38、39和92表现出较强的口服抗真
• 2,4,5-Trisubstituted thiazole derivatives: A novel and potent class of non-nucleoside inhibitors of wild type and mutant HIV-1 reverse transcriptase
  作者：Zhongliang Xu、Mingyu Ba、Hua Zhou、Yingli Cao、Chaojun Tang、Ying Yang、Ricai He、Yu Liang、Xuemei Zhang、Zhenzhong Li、Lihong Zhu、Ying Guo、Changbin Guo

  DOI：10.1016/j.ejmech.2014.07.072

  日期：2014.10

  Novel 2,4,5-trisubstituted thiazole derivatives (TSTs) were designed and synthesized as HIV-1 non-nucleoside reverse transcriptase inhibitors (NNRTIs). Among the thirty-eight synthesized target compounds, thirty TSTs showed potent inhibition against HIV-1 replication in wild type HIV-1 at submicromolar concentrations (from 0.046 to 9.59 mu M). Compounds 21, 23 and 24 were also tested on seven NNRTI-resistant HIV-1 strains, and all exhibited inhibitory effects with fold changes in IC50 ranging from 2.6 to 111, which were better than those of nevirapine (15.6-fold-371-fold). Docking simulations of compound 24 revealed a reasonable mechanism for the binding mode, and three-dimensional quantitative structure activity relationship (3-DQSAR) studies on this novel series of TST further elucidated the structure-activity relationship (SAR). The results suggested the great potential of TSTs as a novel class of NNRTIs with antiviral efficacy and a good resistance profile. (C) 2014 Elsevier Masson SAS. All rights reserved.
• Efficient Synthesis of 3-Aryl-5-chloroindan-1-ones via Free Radical–Mediated Intramolecular Cyclization
  作者：Aeysha Sultan、Abdul Rauf Raza

  DOI：10.1080/00397911.2013.813053

  日期：2014.2

  Abstract An efficient free radical–mediated intramolecular cyclization strategy has been developed for the synthesis of 3-aryl-5-chloroindan-1-ones. Variously substituted 2,4-dichloroenones afforded 3-aryl-5-chloroindan-1-ones in quantitative yields upon intramolecular cyclization under free radical conditions. GRAPHICAL ABSTRACT

  摘要 一种有效的自由基介导的分子内环化策略已被开发用于合成 3-aryl-5-chloroindan-1-ones。在自由基条件下分子内环化后，不同取代的 2,4-二氯烯酮以定量产率提供 3-芳基-5-氯茚满-1-酮。图形概要