3,4,5‐trimethyl‐1‐phenyl‐1H-pyrazole | 10252-57-0

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 唑类
• 英文名称: 3,4,5‐trimethyl‐1‐phenyl‐1H-pyrazole
• 英文别名: 3,4,5-trimethyl-1-phenyl-1H-pyrazole；3,4,5-trimethyl-1-phenylpyrazole；3,4,5-trimethyl-1-phenyl-1H-pyrazole；3,4,5-Trimethyl-1-phenyl-1H-pyrazol；1-Phenyl-3,4,5-trimethyl-pyrazol；3,4,5-Trimethyl-1-phenyl-pyrazol
• CAS: 10252-57-0
• 化学式: C₁₂H₁₄N₂
• mdl: MFCD00996109
• 分子量: 186.257
• InChiKey: UZHVNGNURWBNRG-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.1
• 重原子数：
  14
• 可旋转键数：
  1
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.25
• 拓扑面积：
  17.8
• 氢给体数：
  0
• 氢受体数：
  1

反应信息

• 作为反应物：
  描述：

  3,4,5‐trimethyl‐1‐phenyl‐1H-pyrazole 、 mercury(II) diacetate 在 LiCl 、 acetic acid 作用下， 以 乙醇 、 水 为溶剂， 以49%的产率得到chloro{2-(3',4',5'-trimethylpyrazol-1'-yl)phenyl}mercury(II)
  参考文献：
  名称：

  Black, David St. C.; Deacon, Glen B.; Edwards, Gavin L., Australian Journal of Chemistry, 1993, vol. 46, # 9, p. 1323 - 1336

  摘要：

  DOI：
• 作为产物：
  描述：

  2,4-dimethyl-6,7-benzo-1,5-diazepine 在 四氢呋喃 、 盐酸 、 氨 、 sodium amide 作用下， 生成 3,4,5‐trimethyl‐1‐phenyl‐1H-pyrazole
  参考文献：
  名称：

  Barltrop et al., Journal of the Chemical Society, 1959, p. 1132,1133

  摘要：

  DOI：

文献信息

• Small Molecule Library Synthesis Using Segmented Flow
  作者：Christina M. Thompson、Jennifer L. Poole、Jeffrey L. Cross、Irini Akritopoulou-Zanze、Stevan W. Djuric

  DOI：10.3390/molecules16119161

  日期：——

  Flow chemistry has gained considerable recognition as a simple, efficient, and safe technology for the synthesis of many types of organic and inorganic molecules ranging in scope from large complex natural products to silicon nanoparticles. In this paper we describe a method that adapts flow chemistry to the synthesis of libraries of compounds using a fluorous immiscible solvent as a spacer between reactions. The methodology was validated in the synthesis of two small heterocycle containing libraries. The reactions were performed on a 0.2 mmol scale, enabling tens of milligrams of material to be generated in a single 200 mL reaction plug. The methodology allowed library synthesis in half the time of conventional microwave synthesis while maintaining similar yields. The ability to perform multiple, potentially unrelated reactions in a single run is ideal for making small quantities of many different compounds quickly and efficiently.

  流动化学作为一种简便、高效且安全的合成技术，已获得广泛认可，适用于多种有机和无机分子的制备，其规模从复杂的大型天然产物到硅纳米颗粒不等。本文介绍了一种利用流动化学合成化合物库的方法，该方法采用氟烃不溶性溶剂作为反应间的间隔物。我们在合成两个含小杂环的化合物库中验证了该方法。反应规模为0.2毫摩尔，单次200毫升反应插件即可生成数十毫克的物质。与传统微波合成相比，该方法在保持相似产率的同时，将化合物库合成时间缩短了一半。能够在单次运行中进行多个潜在不相关的反应，这为快速高效地制备少量多种不同化合物提供了理想条件。
• HIV protease inhibiting compounds
  申请人：Flentge Charles A.

  公开号：US20110003827A1

  公开（公告）日：2011-01-06

  A compound of the formula is disclosed as an HIV protease inhibitor. Methods and compositions for inhibiting an HIV infection are also disclosed.

  公开了一种具有以下公式的化合物，作为HIV蛋白酶抑制剂。还公开了抑制HIV感染的方法和组合物。
• Cu_1.5 PMo₁₂ O₄₀ -catalyzed condensation cyclization for the synthesis of substituted pyrazoles
  作者：Guo-Ping Yang、Xing He、Bing Yu、Chang-Wen Hu

  DOI：10.1002/aoc.4532

  日期：2018.11

  A convenient and direct approach has been developed for the preparation of pyrazole derivatives by the condensation cyclization of hydrazines/hydrazide and 1,3‐diketones in the presence of Cu1.5PMo12O40 (0.33 mol%) under mild conditions (r.t.‐60 °C, 10–30 min). Notably, the reaction was found to be scalable as 99% yield was obtained when the reaction was performed at a 5‐mmol scale. This solvent‐free

  在温和的条件下（rt-60），在Cu 1.5 PMo 12 O 40（0.33 mol％）存在下，通过肼/酰肼和1,3-二酮的缩合环化反应，已经开发了一种方便直接的方法来制备吡唑衍生物。°C，10–30分钟）。值得注意的是，当反应在5 mmol规模下进行时，发现该反应可扩展，产率为99％。这种无溶剂和无卤素的催化体系代表了吡唑的一种有效的经济和环保方法。
• Efficient Copper-Catalyzed Synthesis of Substituted Pyrazoles at Room Temperature
  作者：Haifeng Wang、Xiangli Sun、Shuangling Zhang、Guanglu Liu、Chunjie Wang、Lili Zhu、Hui Zhang

  DOI：10.1055/s-0037-1610330

  日期：2018.12

  method for the synthesis of pyrazoles through a copper-catalyzed condensation reaction has been developed. The new catalytic system not only maintained a broad substrate scope but was also active under acid-free reaction conditions, overcoming the conventional requirement for an acid-catalyzed system. Furthermore, the copper catalyst enabled this reaction to be performed at room temperature and in a short

  已开发出一种通过铜催化缩合反应合成吡唑的有效方法。新的催化体系不仅保持了广泛的底物范围，而且在无酸反应条件下也具有活性，克服了对酸催化体系的传统要求。此外，铜催化剂使该反应能够在室温下和较短的反应时间内进行。
• Synthesis of Pyrazoles, Diazepines, Enaminones, and Enamino Esters Using 12-Tungstophosphoric Acid as a Reusable Catalyst in Water
  作者：Zhicai Shang、Jun Wu、Xiang Chen、Jin She、Haifeng Wu、Peizhi Zhang

  DOI：10.1055/s-0028-1083169

  日期：——

  12-Tungstophosphoric acid (H3PW12O40) is found to be an efficient and recyclable catalyst in promoting a chemo- and re­gioselective condensation of hydrazines/hydrazides, diamines, and primary amines with various 1,3-dicarbonyl compounds in pure water at room temperature to afford pyrazoles, diazepines, and enaminones/enamino esters, respectively, in high yields.

  发现12-磷钨酸（H3PW12O40）是一种高效且可循环利用的催化剂，能够在纯水条件下、室温下促进肼/酰肼、二胺及伯胺与多种1,3-二羰基化合物进行化学选择性和区域选择性的缩合反应，分别高产率地生成吡唑、二氮杂环庚烷和烯胺酮/烯胺酯化合物。