3,6-dimethyl-2-(4-methylphenyl)pyrano<4,3-c>pyrazol-4(2H)-one | 106089-53-6

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 唑类
• 英文名称: 3,6-dimethyl-2-(4-methylphenyl)pyrano<4,3-c>pyrazol-4(2H)-one
• 英文别名: 3,6-dimethyl-2-(4-methylphenyl)pyrano[4,3-c]pyrazol-4(2H)-one；3,6-dimethyl-2-(4-methylphenyl)pyrano[4,3-c]pyrazol-4-one
• CAS: 106089-53-6
• 化学式: C₁₅H₁₄N₂O₂
• 分子量: 254.288
• InChiKey: RSISXOGVDYGNHQ-UHFFFAOYSA-N

物化性质

• 熔点：
  172-173 °C(Solv: methanol (67-56-1))
• 沸点：
  416.7±45.0 °C(Predicted)
• 密度：
  1.23±0.1 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  3.1
• 重原子数：
  19
• 可旋转键数：
  1
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.2
• 拓扑面积：
  44.1
• 氢给体数：
  0
• 氢受体数：
  3

反应信息

• 作为产物：
  描述：

  去氢乙酸 在 sodium acetate 、 三氯氧磷 作用下， 以 甲醇 为溶剂， 反应 66.0h， 生成 3,6-dimethyl-2-(4-methylphenyl)pyrano<4,3-c>pyrazol-4(2H)-one
  参考文献：
  名称：

  Pyrano[4,3-c]PYRAZOL-4(1H)-ONES 和 -4(2H)-ONES 的合成和结构的明确分配

  摘要：

  描述了吡喃并吡唑啉酮的清洁合成。4-氯-3-(1-氯乙烯基)-6-甲基-2-吡喃酮与芳基肼的反应产生吡喃并[4,3-c]吡唑-4(2H)-酮作为唯一确定的产物。然而，当使用烷基肼时，已分离出异构吡喃并 [4,3-c] 吡唑-4(1H)-酮。通过同核 1H{1H} NOE 测定可以实现结构的明确分配。

  DOI：

  10.1246/cl.1986.295

文献信息

• Synthesis of Pyrano[4,3-<i>c</i>]pyrazol-4(1<i>H</i>)-ones and -4(2<i>H</i>)-ones from Dehydroacetic Acid. Homo- and Heteronuclear Selective NOE Measurements for Unambiguous Structure Assignment
  作者：Albert Cantos、Pedro de March、Marcial Moreno-Mañas、Anna Pla、Francisco Sanchez-Ferrando、Albert Virgili

  DOI：10.1246/bcsj.60.4425

  日期：1987.12

  Cyclization of dehydroacetic acid N-substituted hydrazones furnished 1-substituted 3,6-dimethylpyrano[4,3-c]pyrazol-4(1H)-ones, together with varying amounts of N,N′-disubstituted 5-hydroxy-3-methyl-4-(3-methyl-1H-pyrazol-5-yl)-1H-pyrazoles. The same pyranopyrazolones were obtained regioselectively without side reactions from N-alkylhydrazines and 4-chloro-3-(1-chlorovinyl)-6-methyl-2H-pyran-2-one

  脱氢乙酸 N-取代腙环化得到 1-取代 3,6-二甲基吡喃并[4,3-c]吡唑-4(1H)-酮，以及不同数量的 N,N'-二取代 5-羟基-3-甲基-4-(3-甲基-1H-吡唑-5-基)-1H-吡唑。N-烷基肼和 4-氯-3-（1-氯乙烯基）-6-甲基-2H-吡喃-2-酮（“脱氢乙酰氯”）在没有副反应的情况下区域选择性地获得了相同的吡喃并吡唑啉酮，而 N-芳基肼得到了2-芳基-3,6-二甲基吡喃并[4,3-c]吡唑-4(2H)-酮。NMR NOE 方法，包括远程选择性异核 13C1H}NOE 增强测量，允许明确区​​分 -4(1H)-ones 和 -4(2H)-ones。
• Design, synthesis, computational and biological evaluation of some new hydrazino derivatives of DHA and pyranopyrazoles
  作者：Ajay Kumar、Poonam Lohan、Deepak K. Aneja、Girish Kumar Gupta、Dhirender Kaushik、Om Prakash

  DOI：10.1016/j.ejmech.2012.01.042

  日期：2012.4

  Two series of compounds namely, 4-aryl/heteroaryl hydrazino-3-acetyl-6-methyl-2H-pyran-2-ones (4a-4j) and pyrano[4,3-c]pyrazoles (6a-6e and 6g) were synthesized starting from 3-acetyl-4-chloro-6-methyl-2H-pyran-2-one (2). Estimation of pharmacotherapeutic potential, possible molecular mechanism of action, toxic/side effects and interaction with drug-metabolizing enzymes were made for the synthesized compounds on the basis of prediction of activity spectra for substances (PASS) prediction results and their analysis by PharmaExpert software. COX inhibition predicted by PASS was confirmed by experimental evaluation and validated via docking studies. Out of all the compounds, compounds 4h, 4j, 6e, 6g exhibited good anti-inflammatory activity, whereas compounds 4b, 4c, 4h, 4i, 4j, 6b, 6e, 6g showed excellent analgesic activity compared with standard drug Diclofenac sodium. (C) 2012 Elsevier Masson SAS. All rights reserved.
• CANTOS, A.;DE, MARCH, P.;MORENO-MANAS, M.;PLA, A.;SANCHEZ-FERRANDO, F.;VI+, CHEM. LETT., 1986, N 3, 295-298
  作者：CANTOS, A.、DE, MARCH, P.、MORENO-MANAS, M.、PLA, A.、SANCHEZ-FERRANDO, F.、VI+

  DOI：——

  日期：——
• CANTOS, ALBERT;MARCH, PEDRO DE;MORENO-MANAS, MARCIAL;PLA, ANNA;SANCHEZ-FE+, BULL. CHEM. SOC. JAP., 60,(1987) N 12, # 4425-4431
  作者：CANTOS, ALBERT、MARCH, PEDRO DE、MORENO-MANAS, MARCIAL、PLA, ANNA、SANCHEZ-FE+

  DOI：——

  日期：——