3-(pivaloxymethyl)pyridine | 859842-81-2

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 吡啶及其衍生物
• 英文名称: 3-(pivaloxymethyl)pyridine
• 英文别名: 2,2-bimethylpropionic acid pyridin-3-ylmethyl ester；Pyridin-3-ylmethyl 2,2-dimethylpropanoate
• CAS: 859842-81-2
• 化学式: C₁₁H₁₅NO₂
• mdl: MFCD27930221
• 分子量: 193.246
• InChiKey: SSFZZSXZIBPJFB-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.9
• 重原子数：
  14
• 可旋转键数：
  4
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.454
• 拓扑面积：
  39.2
• 氢给体数：
  0
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  3-(pivaloxymethyl)pyridine 在 盐酸 、 碳酸氢钠 作用下， 以 甲醇 、 水 、 乙腈 为溶剂， 60.0 ℃ 、1.6 kPa 条件下， 反应 51.0h， 生成 (+)-3,5-diacetoxy-4-N-acetylamino-5-(pivaloxymethyl)cyclopent-1-ene
  参考文献：
  名称：

  Pyridinium Salt Photochemistry in a Concise Route for Synthesis of the Trehazolin Aminocyclitol, Trehazolamine

  摘要：

  A strategy for the concise synthesis of trehazolamine, the aminocyclitol core of the potent trehalase inhibitor trehazolin, has been developed. The methodology takes advantage of photocyclization reaction of 1-methoxyethoxymethyl-3-pivaloxymethylpyridinium perchlorate to generate a bicyclicaziridine intermediate, which is transformed under aziridine ring opening conditions to the key intermediate, 3,5-diacetoxy-3-pivaloxymethyl-4-(N-acetylamino)cyclopentene. In addition, the strategy is used in an enantio-divergent sequence for preparation of the natural (+)-trehazolamine and its unnatural (-)-enantiomer. In this route, the chiral auxiliary containing 1-(tetracetyl-alpha-D-glucosyl)-3-pivaloxymethylpyridinium perchlorate undergoes photocyclization to generate separable, diastereomeric bicyclic-aziridines, which are then independently transformed to enantiomeric 3,5diacetoxy-3-pivaloxymethyl-4-(N-acetylamino)cyclopentenes.

  DOI：

  10.1021/jo050589q
• 作为产物：
  描述：

  3-吡啶甲醇 、 三甲基乙酰氯 在 三乙胺 作用下， 以 二氯甲烷 为溶剂， 生成 3-(pivaloxymethyl)pyridine
  参考文献：
  名称：

  Ni通过C-O键裂解催化芳基酯的甲氧基化

  摘要：

  描述了一种通过空气 裂解对水和不敏感的甲硅烷基锡烷基转移试剂进行镍催化的芳基酯的锡烷基化反应。该协议的特点是适用范围广，包括具有挑战性的组合，因此可以访问通用的构建基块和正交的C-杂原子键形成。

  DOI：

  10.1002/anie.201611720

文献信息

• Substituted Nicotinamide Compounds
  申请人：Hamblett Christopher

  公开号：US20090105264A1

  公开（公告）日：2009-04-23

  The present invention relates to a novel class of substituted nicotinamides. These compounds can inhibit histone deacetylase and are suitable for use in selectively inducing terminal differentiation, and arresting cell growth and/or apoptosis of neoplastic cells, thereby inhibiting proliferation of such cells. Thus, the compounds of the present invention are useful in treating a patient having a tumor characterized by proliferation of neoplastic cells. The compounds of the invention may also be useful in the prevention and treatment of TRX-mediated diseases, such as autoimmune, allergic and inflammatory diseases, and in the prevention and/or treatment of diseases of the central nervous system (CNS), such as neurodegenerative diseases. The present invention further provides pharmaceutical compositions comprising the compounds of the instant invention and safe dosing regimens of these pharmaceutical compositions, which are easy to follow, and which result in a therapeutically effective amount of these compounds in vivo.

  本发明涉及一类新型的替代烟酰胺化合物。这些化合物可以抑制组蛋白去乙酰化酶，适用于选择性诱导终末分化，并阻止肿瘤细胞的生长和/或凋亡，从而抑制这些细胞的增殖。因此，本发明的化合物在治疗具有以肿瘤细胞增殖为特征的患者方面是有用的。本发明的化合物还可能在预防和治疗TRX介导的疾病方面有用，如自身免疫、过敏和炎症性疾病，以及预防和/或治疗中枢神经系统（CNS）疾病，如神经退行性疾病。本发明还提供了包含本发明化合物的药物组合物，以及这些药物组合物的安全用药方案，易于遵循，并在体内产生这些化合物的治疗有效量。
• Oxymethyl Boron Compounds
  申请人：Tanaka Keigo

  公开号：US20080242859A1

  公开（公告）日：2008-10-02

  The present invention provides compounds which are useful as safe substitutes for the organotin reagent used in coupling reaction for the oxymethylation of aromatic rings, such as alkoxymethylation or hydroxymethylation, with a palladium catalyst and which can dispense with chromatographic purification with silica gel in the production and are suitable for mass production; and compounds applicable even to the oxymethylation of aromatic ring substrates which do not permit coupling reaction by conventional technique or have low reactivity.

  本发明提供了一些化合物，可用作在钯催化下进行含氧甲基化反应（如烷氧甲基化或羟基甲基化）的偶联反应中，有机锡试剂的安全替代品。这些化合物可在生产中省去硅胶色谱纯化步骤，并适用于大规模生产；并且这些化合物适用于那些传统技术无法进行偶联反应或反应活性较低的芳环基底物的含氧甲基化反应。
• Condition optimization and kinetic evaluation of Novozym 435-catalyzed synthesis of aroma pyridine esters
  作者：Qianrui Zhao、Xi Zhang、Meng Zhou、Miao Lai、Dingxia Zhou、Yake Wang、Fang Liu、Mingqin Zhao

  DOI：10.1016/j.mcat.2023.113532

  日期：2023.11

  A new method for rapid synthesis of pyridine esters without stirring based on Novozym 435 catalysis had been reported, which was from pyridine methanols and vinyl esters. Based on single factor experiment, the optimization of the enzymatic transesterification was received by response surface methodology (RSM). The high yield of 82% was still reached when Novozym 435 had been recycled 12 times. Under

  报道了一种基于Novozym 435催化、无需搅拌、以吡啶甲醇和乙烯基酯为原料快速合成吡啶酯的新方法。在单因素实验的基础上，采用响应面法（RSM）对酶促酯交换反应进行优化。Novozym 435 循环使用 12 次后，仍能达到 82% 的高产率。在最佳条件下，共合成了22种吡啶酯。通过酶法建立了Novozym 435催化乙酸乙烯酯与3-吡啶甲醇酯交换反应的动力学模型。发现该反应遵循Ping-Pong Bi-Bi机理，并且3-吡啶甲醇抑制该反应。采用气相色谱-质谱-嗅觉测定法（GC-MS-O）分析合成的吡啶酯，3e )、吡啶-3-基甲基肉桂酸酯( 3i )和2-(吡啶-2-基)乙基乙酸酯(3s)具有强烈且优异的香气。通过热重 (TG) 分析发现这三种风味化合物（3e、3i和 3s）在指定温度下具有良好的稳定性。
• HYDROXYMETHYLBORON COMPOUNDS
  申请人：Eisai R&D Management Co., Ltd.

  公开号：EP1867650B1

  公开（公告）日：2012-06-27
• US7696347B2
  申请人：——

  公开号：US7696347B2

  公开（公告）日：2010-04-13