phenyl(pyrimidin-5-yl)methanone | 92674-40-3

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: phenyl(pyrimidin-5-yl)methanone
• 英文别名: phenyl(5-pyrimidinyl)methanone
• CAS: 92674-40-3
• 化学式: C₁₁H₈N₂O
• mdl: MFCD13152939
• 分子量: 184.197
• InChiKey: WWYYPQVGITYPJB-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.5
• 重原子数：
  14
• 可旋转键数：
  2
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.0
• 拓扑面积：
  42.8
• 氢给体数：
  0
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  (3R)-3-ethynyl-1-azabicyclo[2.2.2]oct-3-yl methyl ether 、 phenyl(pyrimidin-5-yl)methanone 在 正丁基锂 作用下， 以 四氢呋喃 、 正己烷 为溶剂， 反应 0.17h， 生成 3-[(3R)-3-methoxy-1-azabicyclo[2.2.2]octan-3-yl]-1-phenyl-1-pyrimidin-5-ylprop-2-yn-1-ol
  参考文献：
  名称：

  Potent anti-muscarinic activity in a novel series of quinuclidine derivatives

  摘要：

  The synthesis and biological evaluation of a novel family of M-3 muscarinic antagonists are described. A systematic modification of the substituents to a novel alkyne-quinuclidine scaffold yielded original compounds displaying potent in vitro anticholinergic properties. (c) 2005 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2005.09.079
• 作为产物：
  描述：

  5-<1-Hydroxy-1-(phenyl)methyl>pyrimidine 在 manganese(IV) oxide 作用下， 以 二氯甲烷 为溶剂， 反应 24.0h， 生成 phenyl(pyrimidin-5-yl)methanone
  参考文献：
  名称：

  Aryl Diazinyl Ketoximes: Synthesis and Configurational Assignment

  摘要：

  Preparation of a series of new aryl diazinyl ketoximes (7a,b - 12a,b) required as synthetic building blocks is described. Separation of the E/Z-isomers obtained was achieved by means of chromatography, their configuration was assigned using nmr techniques. Moreover, procedures for the synthesis of the starting ketones (1b - 6b) are given.

  DOI：

  10.3987/com-95-7248

文献信息

• Carbonylative Hiyama coupling of aryl halides with arylsilanes under balloon pressure of CO
  作者：Sheng Chang、Ying Jin、Xiu Rong Zhang、Yong Bing Sun

  DOI：10.1016/j.tetlet.2016.02.058

  日期：2016.5

  An efficient protocol has been developed for the carbonylative Hiyama coupling of aryl halides using the cesium fluoride as a promoter by palladium-catalyzed in NMP. This protocol was applied to a wide variety of functionalized and hindered aryl iodides and bromides with arylsilanes, to afford the desired biaryl ketones in good to excellent yields.

  已经开发了一种有效的方案，用于将氟化铯作为促进剂，通过钯在NMP中催化，对芳基卤化物进行羰基化Hiyama偶联。该方案适用于各种带有芳基硅烷的官能化和受阻的芳基碘化物和溴化物，以良好至极佳的收率提供所需的联芳基酮。
• OLED材料中间体苯甲酰嘧啶类化合物的合 成方法
  申请人：棓诺(苏州)新材料有限公司

  公开号：CN108148003B

  公开（公告）日：2021-03-26

  本发明公开了一种苯甲酰嘧啶类化合物的合成方法，包括步骤：碱、溶剂Ⅰ以及作为原料的取代苯乙酮和草酸二酯混合后进行反应，得中间体Ⅰ；中间体Ⅰ、溶剂Ⅱ以及作为原料的二胺类化合物和原甲酸三酯混合后进行反应，得中间体Ⅱ；中间体Ⅱ与乙醇、乙酸混合后进行反应，得中间体Ⅲ；中间体Ⅲ与乙醇水溶液混合后再加入碱进行反应，得中间体Ⅳ；中间体Ⅳ和溶剂Ⅲ混合后反应，得作为目标产物的苯甲酰嘧啶类化合物。本发明的苯甲酰嘧啶类化合物的合成方法，采用价廉、易得的原料，以简便、温和的条件合成苯甲酰嘧啶类化合物。
• Carbonylative coupling of aryl tosylates/triflates with arylboronic acids under CO atmosphere
  作者：Cheng Yi Hao、Dan Wang、Ya Wei Li、Lin Lin Dong、Ying Jin、Xiu Rong Zhang、He Yun Zhu、Sheng Chang

  DOI：10.1039/c6ra14678c

  日期：——

  The carbonylative Suzuki–Miyaura reaction between aryl tosylates/triflates with arylboronic acid is herein reported, using base-free conditions and a balloon pressure of carbon monoxide. Under these conditions, unsymmetrical biaryl ketones were obtained in modest to excellent yields. This method was adapted to the synthesis of oxybenzone and ketoprofen in good yields under mild conditions.

  本文报道了在无碱条件和一氧化碳的球囊压力下，芳基甲苯磺酸盐/三氟甲磺酸与芳基硼酸之间的羰基化Suzuki-Miyaura反应。在这些条件下，以中等至极好的收率获得了不对称的联芳基酮。该方法适合在温和条件下以高收率合成氧苯甲酮和酮洛芬。
• Quinuclidine derivatives processes for preparing them and their uses as m2 and/or m3 muscarinic receptor inhibitors
  申请人：Guyaux Michel

  公开号：US20050020660A1

  公开（公告）日：2005-01-27

  The invention concerns quinuclidine derivatives of formula I or II wherein the substituents are as defined in the specification, as well as their use as pharmaceuticals. The compounds of the invention_show high affinities for m3 and/or m2 muscarinic receptors and are particularly suited for treating urinary incontinence.

  本发明涉及式I或II的季铵盐衍生物，其中取代基如规范中所定义，以及它们作为药物的用途。本发明的化合物具有高亲和力m3和/或m2胆碱能受体，特别适用于治疗尿失禁。
• Suzuki coupling of aroyl-MIDA boronate esters – A preliminary report on scope and limitations
  作者：Samson Lai、Noah Takaesu、Wen Xuan Lin、David M. Perrin

  DOI：10.1016/j.tetlet.2021.153147

  日期：2021.6