CAS: 18088-01-2; (2,6-Dimethylpyridin-4-yl)Methanol

该化合物是一种衍生物,在2个和6个位置的4个位置和替代单位的4个位置上形成一个羟基甲基功能组和甲基替代组,该化合物是有机合成的多用途中间体,特别是在制药,农用化学品和协调综合体的准备中.该化合物的固态阻力核心增强了稳定性,而氢氧甲基组则为进一步功能化提供了一个反应场所,如酯化或氧化.该化合物的固定结构和纯度使其适合在药用化学和催化中精确应用.其在普通有机溶剂中的溶解性有利于在合成工作流程中进行处理.建议在惰性条件下进行储存以保持稳定性.

结构式图片

相似化合物

54221-93-1 18206-06-9 142896-15-9

上下游产品

CAS号1073-23-0 2,6-二甲基吡啶 N-氧化物 | CAS号108-48-5 2,6-二甲基吡啶 | CAS号18206-06-9 2,6-二甲基吡啶-4-甲醛 | CAS号120739-87-9 2,6-二甲基-4-氯甲基吡啶 | CAS号79313-02-3 4-(溴甲基)-2,6-二甲基吡啶

合成工艺路线路线简述

  • 合成目标产物 (2,6-Dimethylpyridin-4-yl)Methanol 主要起始原料 Methanol And Ethanamine, N-[(3,5-Dichlorophenyl)Methylene]-2,2-Diethoxy-
  • (文献来源)合成步骤主要原料 Methanol 和 Ethanamine, N-[(3,5-Dichlorophenyl)Methylene]-2,2-Diethoxy-
📜2,6-二甲基吡啶 N-氧化物置于dipotassium Peroxodisulfate体系中,用 二氯甲烷,水 用作溶剂,化学反应 6.0H,反应生成2,6-二甲基-3-羟甲基吡啶
参考文献:Selective Photosensitization Through An And Logic Response: Optimization Of The Ph And Glutathione Response Of Activatable Photosensitizers
标题:Selective Photosensitization Through An And Logic Response: Optimization Of The Ph And Glutathione Response Of Activatable Photosensitizers
摘要:一个分子and逻辑门,即一种可激活的光敏剂,需要超过阈值的酸性(ph)和gsh才能发挥全部活性.
Doi:10.1039/c5Cc01261A

海关参考信息

专利信息


专利号:US-5736535-A
优先权日:1992-04-16
标 题:1-pyrimidinylacetamide compounds which are inhibitors of human leukocyte elastase
发明人:BERNSTEIN PETER ROBERT; EDWARDS PHILIP DUKE; SHAW ANDREW; SHENVI ASHOKKUMAR BHIKKAPPA; THOMAS ROYSTON MARTIN; VEALE CHRIS ALLAN; WARNER PETER; WOLANIN DONALD JOHN
权利人:ZENECA LTD
摘要:The present invention relates to certain novel substituted derivatives which are 1-pyrimidinylacetamide derivatives of formula I, ##STR1## which are inhibitors of human leukocyte elastase (HLE), also known as human neutrophil elastase (HNE), making them useful whenever such inhibition is desired, such as for research tools in pharmacological, diagnostic and related studies and in the treatment of diseases in mammals in which HLE is implicated. The invention also includes intermediates useful in the synthesis of these substituted derivatives, processes for preparing the substituted derivatives, pharmaceutical compositions containing such substituted derivatives and methods for their use.

专利号:US-5254558-A
优先权日:1991-08-15
标 题:Substituted 1,3-diazines as leukocyte elastase inhibitors
发明人:BERNSTEIN PETER R; EDWARDS PHILIP D; THOMAS ROYSTON M; VEALE CHRIS A; WARNER PETER; WOLANIN DONALD J
权利人:ICI PLC
摘要:The present invention relates to certain novel substituted heterocycles which are 1-pyrimidinylacetamide compounds of formula I, set out herein, which are inhibitors of human leukocyte elastase (HLE), also known as human neutrophil elastase (HNE), making them useful whenever such inhibition is desired, such as for research tools in pharmacological, diagnostic and related studies and in the treatment of diseases in mammals in which HLE is implicated. The invention also includes intermediates useful in the synthesis of these substituted heterocycles, processes for preparing the substituted heterocycles, pharmaceutical compositions containing such substituted heterocycles and methods for their use.

专利号:US-5521179-A
优先权日:1991-04-18
标题 :Heterocyclic amides
发明人:BERNSTEIN PETER R; SHAW ANDREW; THOMAS ROYSTON M; WARNER PETER; WOLANIN DONALD J
权利人:ZENECA LTD
摘要:The present invention relates to certain novel heterocyclic amides which are 1-pyridylacetamide compounds of formula I, set out herein, which are inhibitors of human leukocyte elastase (HLE), also known as human neutrophil elastase (HNE), making them useful whenever such inhibition is desired, such as for research tools in pharmacological, diagnostic and related studies and in the treatment of diseases in mammals in which HLE is implicated. The invention also includes intermediates useful in the synthesis of these heterocyclic amides, processes for preparing the heterocyclic amides, pharmaceutical compositions containing such heterocyclic amides and methods for their use.

供应商参考报价(招募中)

品牌试剂参考报价(招募中)

📌 第三方产品分析报告

✅ COA系统入驻 | 共享模式
📝 需求与反馈
尽可能描述清楚需求与问题信息
×

通知