3-(4-Methylsulfanylphenyl)-1-(3-nitrophenyl)prop-2-en-1-one | 121646-10-4

• 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
• 英文名称: 3-(4-Methylsulfanylphenyl)-1-(3-nitrophenyl)prop-2-en-1-one
• CAS: 121646-10-4
• 化学式: C₁₆H₁₃NO₃S
• 分子量: 299.35
• InChiKey: SZXXHUPKVVISFF-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4
• 重原子数：
  21
• 可旋转键数：
  4
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.06
• 拓扑面积：
  88.2
• 氢给体数：
  0
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  异烟肼 、 3-(4-Methylsulfanylphenyl)-1-(3-nitrophenyl)prop-2-en-1-one 以 neat (no solvent) 为溶剂， 以92%的产率得到(5-(4-(methylthio)phenyl)-3-(3-nitrophenyl)-4,5-dihydro-1H-pyrazol-1-yl)(pyridin-4-yl)methanone
  参考文献：
  名称：

  一种用于吡唑啉区域选择性合成的权宜之计、一锅法、逐步顺序方法

  摘要：

  通过使用查耳酮和吡啶-4-碳酰肼的单锅、逐步、顺序方法，描述了一种合成吡唑啉/吡唑系吡啶基甲酮的有效方法。

  DOI：

  10.1177/1747519820977165
• 作为产物：
  描述：

  4-(甲基巯基)苯甲醛 、 间硝基苯乙酮 在 alkali hydroxide 作用下， 以 乙醇 为溶剂， 反应 4.0h， 生成 3-(4-Methylsulfanylphenyl)-1-(3-nitrophenyl)prop-2-en-1-one
  参考文献：
  名称：

  一种用于吡唑啉区域选择性合成的权宜之计、一锅法、逐步顺序方法

  摘要：

  通过使用查耳酮和吡啶-4-碳酰肼的单锅、逐步、顺序方法，描述了一种合成吡唑啉/吡唑系吡啶基甲酮的有效方法。

  DOI：

  10.1177/1747519820977165

文献信息

• Novel 1,3,5-triphenyl-2-pyrazolines as anti-infective agents
  作者：P.M. Sivakumar、S. Prabhu Seenivasan、Vanaja Kumar、Mukesh Doble

  DOI：10.1016/j.bmcl.2010.03.083

  日期：2010.5

  Sixteen 1,3,5-triphenyl-2-pyrazolines were synthesized and their anti-infective activities (against Mycobacterium tuberculosis H(37)Rv, six bacterial and four fungal strains) were tested. Only compound with SO(2)CH(3) in the para position of the A-ring was active against the tubercular strain at 100 mu g/ml concentration. All compounds showed good anti infective activity against Escherichia coli and poor activity against Staphylococcus aureus. Compounds 4, 12, 13 and 14 exhibited reasonable activity against all the organisms tested (<0.309 mu M except against S. aureus. The activity of these compounds correlated with their lipophilic/hydrophilic nature. Compounds 4, 10 and 16 showed very good activity (>88% reduction) against four fungi studied at 2 mg/ml. All these compounds possess halogen substitutions. Compound 11 showed very high activity (>90%) against three fungi. Majority of the compounds showed more than 90% inhibition against one or two fungi. Since pyrazolines are reported to inhibit the activity of p-glycoprotein, they may prevent drug resistance developed by microorganism. (C) 2010 Elsevier Ltd. All rights reserved.
• Synthesis, antioxidant evaluation, and quantitative structure–activity relationship studies of chalcones
  作者：P. M. Sivakumar、P. K. Prabhakar、M. Doble

  DOI：10.1007/s00044-010-9342-1

  日期：2011.5

  Synthesis, antioxidant activity, and quantitative structure-activity relationship (QSAR) of 25 of chalcone derivatives is reported here. They were synthesized by Claisen-Schmidt reaction and were characterized by FTIR, NMR, and mass spectroscopy. Antioxidant activity is evaluated through four different methods namely, superoxide radical-scavenging, hydrogen peroxide scavenging, reducing power, and DPPH radical-scavenging assays. Generally, compounds with -SCH3 and -OCH3 in the para position of the A-ring and -OH in the B-ring were more active than others. In few cases some of the compounds were more active than ascorbic acid or butylated hydroxytoluene. QSAR was developed correlating the antioxidant activity with the structural features of the compounds and the predictive capability of the models was estimated using internal and external validation methods. All the predictions were within the 99% confidence level. Spatial, structural, and lipophilic properties of the compounds determine their antioxidant properties.
• An expedient, one-pot, stepwise sequential approach for the regioselective synthesis of pyrazolines
  作者：Suresh Ganesan、Muniraj Sarangapani、Mukesh Doble

  DOI：10.1177/1747519820977165

  日期：2021.3

  An efficient approach for the synthesis of pyrazoline/pyrazole-tethered pyridinyl methanones is described via a one-pot, stepwise, sequential methodology using chalcones and pyridine-4-carbohydrazi...

  通过使用查耳酮和吡啶-4-碳酰肼的单锅、逐步、顺序方法，描述了一种合成吡唑啉/吡唑系吡啶基甲酮的有效方法。