CAS: 485799-04-0; 4-(5-(4,4,5,5-Tetramethyl-1,3,2-Dioxaborolan-2-yl)Pyridin-2-yl)Morpholine

该化合物是一种化学化合物,其特点是其碳酸性能,这对药用化学和有机合成的应用至关重要.环的存在有助于其芳香特性,而环组则会增强其溶性及潜在的生物活动.由于极生酸多味和多液性芳烃和单磷酸成分的结合,该化合物通常具有中等极极极性.它经常用于交叉反应,特别是形成碳-碳结,使其在复杂的有机分子合成中具有价值.酸酯组在反应过程中保护酸,允许选择性转化.此外,该化合物的稳定性和再活性可能受到诸如pH和温度等环境因素的影响.

结构式图片

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904326-93-8 1356068-62-6 1684430-48-5

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CAS号73183-34-3 双戊酰二硼 | CAS号200064-11-5 5-溴-2-吗啉吡啶

合成工艺路线路线简述

    5-溴-2-氯吡啶置于1,1'-双(二苯膦基)二茂铁二氯化钯(II)二氯甲烷复合物,Potassium Acetate,Caesium Carbonate体系中,用 1,4-二氧六环,N,N-二甲基甲酰胺 作为反应溶剂,化学反应 14.0H,反应生成 6-(吗啉-4-基)吡啶-3-硼酸频哪醇酯
    参考文献:Wo2020081636A5
    标题:Wo2020081636A5

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    专利信息


    专利号:US-7638633-B2
    优先权日:2005-02-21
    标题 :Process for synthesis of proton pump inhibitors
    发明人:PATHI SRINIVAS LAXMINARAYAN; KANKAN RAJENDRA NARAYANRAO; RAO DHARMARAJ RAMACHANDRA
    权利人:CIPLA LTD
    摘要:A process for preparation of rabeprazole sodium comprising oxidation of wet or dry rabeprazole sulphide with sodium hypohalite in water or a mixture of water and water miscible solvent using alkali metal hydroxide and catalyst is disclosed herein. The present invention also discloses process for preparation of rabeprazole sulphide.

    专利号:EP-2354120-A1
    优先权日:2003-08-20
    标题 :Synthesis of acyloxyalkyl carbamate prodrugs and intermediates thereof
    发明人:GALLOP MARK A; YAO FENMEI; LUDWIKOW MARIA J; PHAN THU; PENG GE
    权利人:XENOPORT INC
    摘要:The present invention relates to acyloxyalkyl carbamate prodrugs of (±)-4-amino-3-(4-fluorophenyl)butanoic acid and analogs thereof, pharmaceutical compositions thereof, methods of making prodrugs of (±)-4-amino-3-(4-fluorophenyl)butanoic acid and analogs thereof, methods of using prodrugs of (±)-4-amino-3-(4-tluorophenyl)butanoic acid and analogs thereof, and pharmaceutical compositions thereof for treating or preventing common diseases and/or disorders such as spasticity and/or acid reflux disease. The present invention also relates to acyloxyalkyl carbamate prodrugs of (±)-4-amino-3-(4-fluorophenyl)butanoic acid and analogs thereof which are suitable for oral administration and to sustained release oral dosage forms thereof.

    专利号:AT-E473222-T1
    优先权日:2005-02-21
    标 题:NEW METHOD FOR SYNTHESIS OF PROTON PUMP INHIBITORS

    专利号:US-7935686-B2
    优先权日:2004-11-03
    标 题 :Acyloxyalkyl carbamate prodrugs, methods of synthesis, and use
    发明人:GALLOP MARK A
    权利人:XENOPORT INC
    摘要:Acyloxyalkyl carbamate prodrugs of 3-aminopropylphosphonous acid, 3-aminopropylphosphinic acid, and analogs thereof, pharmaceutical compositions comprising acyloxyalkyl carbamate prodrugs of 3-aminopropylphosphonous acid, 3-aminopropylphosphinic acid, and analogs thereof, methods of making prodrugs of 3-aminopropylphosphonous acid, 3-aminopropylphosphinic acid, and analogs thereof, methods of using prodrugs of 3-aminopropylphosphonous acid, 3-aminopropylphosphinic acid, and analogs thereof and pharmaceutical compositions thereof for treating or preventing diseases or disorders such as spasticity or gastroesophageal reflux disease are disclosed. Acyloxyalkyl carbamate prodrugs of 3-aminopropylphosphonous acid, 3-aminopropylphosphinic acid, and analogs thereof and sustained release oral dosage forms thereof, which are suitable for oral administration, are also disclosed.

    专利号:US-2008161579-A1
    优先权日:2005-02-21
    标题 :Process for Synthesis of Proton Pump Inhibitors

    专利号:US-7566738-B2
    优先权日:2004-11-03
    标题 :Acyloxyalkyl carbamate prodrugs of sulfinic acids, methods of synthesis, and use
    发明人:GALLOP MARK A
    权利人:XENOPORT INC
    摘要:Acyloxyalkyl carbamate prodrugs of 3-aminopropylsulfinic acid and analogs thereof, pharmaceutical compositions of 3-aminopropylsulfinic acid and analogs thereof, methods of making prodrugs of 3-aminopropylsulfinic acid and analogs thereof, methods of using prodrugs of 3-aminopropylsulfinic acid and analogs thereof, and pharmaceutical compositions thereof for treating or preventing diseases or disorders such as spasticity or gastroesophageal reflux disease are disclosed. Acyloxyalkyl carbamate prodrugs of 3-aminopropylsulfinic acid and analogs thereof and sustained release oral dosage forms thereof, which are suitable for oral administration, are also disclosed.
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    合成参考文献


    摘要:Mérour, J.-Y.; Joseph, B., Science of Synthesis Knowledge Updates, (2016) 3, 399.
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