5-methoxy-2-(4-methoxyphenyl)-3-phenyl-2H-indazole | 848142-79-0

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 唑类
• 英文名称: 5-methoxy-2-(4-methoxyphenyl)-3-phenyl-2H-indazole
• 英文别名: 5-Methoxy-2-(4-methoxyphenyl)-3-phenylindazole
• CAS: 848142-79-0
• 化学式: C₂₁H₁₈N₂O₂
• 分子量: 330.386
• InChiKey: JTYBKVBJXJESAD-UHFFFAOYSA-N

物化性质

• 熔点：
  138-140 °C(Solv: ethyl acetate (141-78-6); hexane (110-54-3))
• 沸点：
  408.4±37.0 °C(Predicted)
• 密度：
  1.16±0.1 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  4.8
• 重原子数：
  25
• 可旋转键数：
  4
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.1
• 拓扑面积：
  36.3
• 氢给体数：
  0
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  5-methoxy-2-(4-methoxyphenyl)-3-phenyl-2H-indazole 在 三氟二甲基硫醚络合物 作用下， 以 二氯甲烷 为溶剂， 反应 48.0h， 以77%的产率得到2-(4-Hydroxyphenyl)-3-phenylindazol-5-ol
  参考文献：
  名称：

  Indazole Estrogens:  Highly Selective Ligands for the Estrogen Receptor β

  摘要：

  The estrogen receptors, ERalpha and ERbeta, are important pharmaceutical targets. To develop ERbeta-selective ligands, we synthesized a series of nonsteroidal compounds having a phenyl-2H-indazole core with different groups at C-3. Several of these show high affinity and good ERbeta selectivity, especially those with polar and/or polarizable substituents at this site (halogen, CF3, nitrile); the best compounds have affinities for ERbeta comparable to estradiol, with ERbeta affinity selectivity > 100. This potency and ERbeta selectivity is also seen in cell-based transcriptional assays, where several compounds showed ERbeta efficacies equivalent to that of estradiol with ERbeta potency selectivities of 100. These compounds might prove useful as selective pharmacological probes to study the biological actions of estrogens mediated through ERP, and they might lead to the development of useful pharmaceuticals. These findings also contribute to an evolving pharmacophore that characterizes certain nonsteroidal ligands having high ERbeta subtype affinity and potency selectivity.

  DOI：

  10.1021/jm049223g
• 作为产物：
  描述：

  4-甲氧基苯肼盐酸盐 在 1,1'-双(二苯基膦)二茂铁 、 palladium diacetate 、 tris(dibenzylideneacetone)dipalladium (0) 、 溴 、 sodium hexamethyldisilazane 、 溶剂黄146 、 三(邻甲基苯基)磷 、 sodium t-butanolate 作用下， 以 四氢呋喃 、 N,N-二甲基甲酰胺 、 甲苯 为溶剂， 反应 32.25h， 生成 5-methoxy-2-(4-methoxyphenyl)-3-phenyl-2H-indazole
  参考文献：
  名称：

  Indazole Estrogens:  Highly Selective Ligands for the Estrogen Receptor β

  摘要：

  The estrogen receptors, ERalpha and ERbeta, are important pharmaceutical targets. To develop ERbeta-selective ligands, we synthesized a series of nonsteroidal compounds having a phenyl-2H-indazole core with different groups at C-3. Several of these show high affinity and good ERbeta selectivity, especially those with polar and/or polarizable substituents at this site (halogen, CF3, nitrile); the best compounds have affinities for ERbeta comparable to estradiol, with ERbeta affinity selectivity > 100. This potency and ERbeta selectivity is also seen in cell-based transcriptional assays, where several compounds showed ERbeta efficacies equivalent to that of estradiol with ERbeta potency selectivities of 100. These compounds might prove useful as selective pharmacological probes to study the biological actions of estrogens mediated through ERP, and they might lead to the development of useful pharmaceuticals. These findings also contribute to an evolving pharmacophore that characterizes certain nonsteroidal ligands having high ERbeta subtype affinity and potency selectivity.

  DOI：

  10.1021/jm049223g

文献信息

• Rhenium-Catalyzed [4 + 1] Annulation of Azobenzenes and Aldehydes via Isolable Cyclic Rhenium(I) Complexes
  作者：Xiaoyu Geng、Congyang Wang

  DOI：10.1021/acs.orglett.5b00938

  日期：2015.5.15

  The first Re-catalyzed [4 + 1] annulation of azobenzenes with aldehydes was developed to furnish 2H-indazoles via isolable and characterized cyclic ReI-complexes. For the first time, the acetate-acceleration effect is showcased in Re-catalyzed C–H activation reactions. Remarkably, mechanistic studies revealed an irreversible aldehyde-insertion step, which is in sharp contrast to those of previous Rh-

  首次开发了用醛对偶氮苯进行再催化的[4 +1]环合反应，以通过可分离和表征的环状Re I-络合物提供2 H-吲唑。在重新催化的C–H活化反应中，乙酸促进作用首次显示出来。值得注意的是，机理研究表明，醛的插入步骤不可逆，这与以前的Rh和Co体系的形成强烈反差。
• Rh(III)-Catalyzed [4 + 1]-Annulation of Azoxy Compounds with Alkynes: A Regioselective Approach to 2<i>H</i>-Indazoles
  作者：Zhen Long、Yudong Yang、Jingsong You

  DOI：10.1021/acs.orglett.7b00982

  日期：2017.6.2

  A rhodium-catalyzed regioselective C–H activation/cyclization of azoxy compounds with alkynes has been disclosed to construct a variety of 2H-indazoles. A [4 + 1]-cycloaddition rather than a normal [4 + 2] mode is observed in the process of cyclative capture along with an oxygen-atom transfer and a C≡C triple bond cleavage. This protocol features a broad substrate scope, a good functional group tolerance

  铑催化炔烃对偶氮化合物的区域选择性C–H活化/环化反应已被证实可构建多种2 H-吲唑。在循环捕获的过程中观察到[4 +1]-环加成而不是正常的[4 +1]模式，以及氧原子转移和C≡C三键裂解。该协议具有广泛的底物范围，良好的官能团耐受性和独特的区域选择性。
• Tosyl Hydrazine-Promoted Tandem Condensation and Cyclization of Acyl Azobenzenes Enabling Access to 2<i>H</i> -Indazoles under Metal-Free Aerobic Conditions
  作者：Jeong-Yu Son、Hyunseok Kim、Yonghyeon Baek、Kyusik Um、Gi Hoon Ko、Gi Uk Han、Sang Hoon Han、Kooyeon Lee、Phil Ho Lee

  DOI：10.1002/adsc.201801055

  日期：2018.11.16

  Tosyl hydrazine‐promoted tandem condensation and cyclization of 2‐acyl azobenzenes under metal‐free aerobic conditions was demonstrated to give 2‐aryl‐2H‐indazoles having alkyl‐ or aryl groups at the 3‐position in quantitative yields through the release of water, molecular nitrogen, and sulfinic acid. All of the examples produced the corresponding 2H‐indazoles in quantitative yields. The present reaction

  甲苯磺酰肼促进的串联缩合反应和2-酰基偶氮苯在无金属的好氧条件下的环化反应可通过释放水以定量收率得到在3位具有烷基或芳基的2-芳基2 H-吲唑，分子氮和亚磺酸。所有实施例均以定量产率产生了相应的2 H-吲唑。确定本反应具有宽的底物范围和良好的官能团耐受性。
• Direct Access to Acylated Azobenzenes via Pd-Catalyzed C–H Functionalization and Further Transformation into an Indazole Backbone
  作者：Hongji Li、Pinhua Li、Lei Wang

  DOI：10.1021/ol303434n

  日期：2013.2.1

  Azobenzenes were readily acylated at the 2-position through a Pd-catalyzed C-H functionalization from simple aromatic azo compounds and aldehydes in good yields. The obtained acylated azobenzenes could be efficiently converted into the corresponding indazole derivatives in nearly quantitative yields.
• Indazole Estrogens:  Highly Selective Ligands for the Estrogen Receptor β
  作者：Meri De Angelis、Fabio Stossi、Kathryn A. Carlson、Benita S. Katzenellenbogen、John A. Katzenellenbogen

  DOI：10.1021/jm049223g

  日期：2005.2.1

  The estrogen receptors, ERalpha and ERbeta, are important pharmaceutical targets. To develop ERbeta-selective ligands, we synthesized a series of nonsteroidal compounds having a phenyl-2H-indazole core with different groups at C-3. Several of these show high affinity and good ERbeta selectivity, especially those with polar and/or polarizable substituents at this site (halogen, CF3, nitrile); the best compounds have affinities for ERbeta comparable to estradiol, with ERbeta affinity selectivity > 100. This potency and ERbeta selectivity is also seen in cell-based transcriptional assays, where several compounds showed ERbeta efficacies equivalent to that of estradiol with ERbeta potency selectivities of 100. These compounds might prove useful as selective pharmacological probes to study the biological actions of estrogens mediated through ERP, and they might lead to the development of useful pharmaceuticals. These findings also contribute to an evolving pharmacophore that characterizes certain nonsteroidal ligands having high ERbeta subtype affinity and potency selectivity.