CAS: 107264-09-5; 1-Fluoropyridin-1-Ium Tetrafluoroborate

该化合物是一种以有硅化物和四氟乙酸阴离子为特征的离子化合物; 酸盐的产物为丙烯酯,一种六人芳香环,内含一个氮原子,有助于其在极溶剂中的基本性和溶解性; 四氟乙酸酯阴离子是一种高度稳定且不协调的电离子(以其四氟原子结结为原子的强电密度而著称); 这种化合物通常用于有机合成,并在各种化学反应中用作试剂,特别是在氟化领域; 具有高热稳定性和低挥发性等特性,因此适合在实验室和工业环境中应用; 此外,由于氟化物的存在,它可能呈现出与其他类似的化合物相比独特的再活性模式. 在处理该物质时,应当采取安全防范措施,因为该物质可能具有集中形式的危险.

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CAS号110-86-1 吡啶 | CAS号372-48-5 2-氟吡啶 | CAS号1628-89-3 2-甲氧基吡啶 | CAS号4783-68-0 2-苯氧基吡啶 | CAS号21418-21-3 2-(氰基氨基)吡啶 | CAS号25700-14-5 2-咪唑-1-吡啶 | CAS号5231-96-9 2-乙酰氨基吡啶 | CAS号153653-00-0 METHYL 4-(PYRID... | CAS号3145-77-5 2-[(甲硫基)甲基]吡啶 | CAS号4589-12-2 N-(吡啶-2-基)苯甲酰胺 | CAS号33957-35-6 4H-Pyrido[1,2-a...

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    参考文献:Umemoto,Teruo;Harasawa,Kikuko;Tomizawa,Ginjiro;Kawada,Kosuke;Tomita,+,Bull. Chem. Soc. Jap.,64,(1991) N,C. 1081-1092
    标题:Umemoto,Teruo;Harasawa,Kikuko;Tomizawa,Ginjiro;Kawada,Kosuke;Tomita,+,Bull. Chem. Soc. Jap.,64,(1991) N,C. 1081-1092

    专利信息


    专利号:US-2023287032-A1
    优先权日:2020-08-14
    标 题:Synthesis of fluorinated nucleotides
    发明人:CHUNG CHEOL KEUN; LIU ZHIJIAN; MALIGRES PETER E; MAO EDNA; OBLIGACION JENNIFER V; PHILLIPS ERIC M; PIRNOT MICHAEL; POIRIER MARC; SONG ZHIGUO JAKE; WANG TAO
    权利人:CHUNG CHEOL KEUN; LIU ZHIJIAN; MALIGRES PETER E; MAO EDNA; OBLIGACION JENNIFER V; PHILLIPS ERIC M; PIRNOT MICHAEL; POIRIER MARC; SONG ZHIGUO JAKE; WANG TAO; MERCK SHARP & DOHME LLC
    摘要:The present invention relates to efficient processes useful in the preparation of fluorinated nucleosides, such as (O—{[(2R,3R,4S,5R)-5-(6-amino-9H-purin-9-yl)-4-fluoro-3-hydroxyoxolan-2-yl]methyl}O,O-dihydrogen phosphorothioate, also known as 2′-(S)-fluoro-thio-adenosine monophosphate or 2′-F-thio-AMP. Such fluorinated nucleosides may be useful as a biologically active compound and or as an intermediate for the synthesis of more complex biologically active compounds. The present invention also encompasses intermediates useful in the disclosed synthetic processes and the methods of their preparation.

    专利号:US-2023174567-A1
    优先权日:2020-05-22
    标题:Synthesis of fluorinated nucleotides
    发明人:ARMIGER TRAVIS; BELYK KEVIN M; BENKOVICS TAMAS; CHUNG CHEOL K; JI CHEN YINING; JOHNSON HEATHER CLAIRE; KLAPARS ARTIS; LIU ZHIJIAN; LIU ZHUQING; MOORE JEFFREY C; NEEL ANDREW J; PENG FENG; RUMMELT STEPHAN M; SALEHI MARZUARANI NASTARAN; SHERRY BENJAMIN D; SONG ZHIGUO JAKE; TURNBULL BEN WILLIAM HULME; WANG LU; XU FENG
    权利人:MERCK SHARP & DOHME LLC
    摘要:The present invention relates to efficient processes useful in the preparation of fluorinated nucleosides, such as (2S,3R,4S,5R)-5-(2-amino-6-oxo-1,6-dihydro-9H-purin-9-yl)-3-fluoro-4-hydroxy-2-(mercaptomethyl)tetrahydrofuran-3-yl dihydrogen phosphate, also known as 3′-fluoro-thio-guanosine monophosphate or 3′-F-thio-GMP. Such fluorinated nucleosides may be useful as a biologically active compound and or as an intermediate for the synthesis of more complex biologically active compounds. The present invention also encompasses intermediates useful in the disclosed synthetic processes and the methods of their preparation. (I)

    专利号:US-2024239924-A1
    优先权日:2021-04-30
    标题:Synthesis of sulfonyl halide terminated polyethylene
    发明人:BROONER RACHEL E M; SENECAL TODD D; KEAN ZACHARY S
    权利人:DOW GLOBAL TECHNOLOGIES LLC
    摘要:Methods for preparing end-functionalized polyolefin, The methods include polymerizing one or more olefin monomers in the presence of an aluminum chain transfer agent to produce a polymeryl aluminum species; treating the polymeryl aluminum species with sulfur oxide compound at a reactor temperature to form a polymeryl sulfinate; and oxidizing the polymeryl sulfinate; wherein the end-functionalized polyolefin comprises a polymer backbone having at least 30 carbon atoms; and the end-functionalized polyolefin comprises a sulfur containing group,

    专利号:EP-1422235-B1
    优先权日:2001-07-26
    标题 :Stereoselective method of producing 6alpha-fluoropregnanes and intermediaries
    发明人:MURILLO GARRIDO JOSE VICENTE; SILVA GUISASOLA LUIS OCTAVIO; MARTIN JUAREZ JORGE
    权利人:RAGACTIVES SL
    摘要:6 alpha -fluorpregnanes (I), where the dotted line between positions 1 and 2 represents a single or double bond; R1 is OH, OCOR2, X, SO3R3, or an (R7)(R8)(R9)SiO- group, where X is halogen, R2 and R3 are C1-6 alkyl or phenyl optionally substituted by C1-4 alkyl, and R7, R8 and R9, equal or different, are C1-6 alkyl or phenyl optionally substituted by C1-4 alkyl, can be obtained by means of a high stereoselectivity process comprising reacting a 3-(trisubstituted)silyloxy-pregna-3,5-diene (IV) with a fluorinating agent selected among N-fluorosulfonimides and N-fluorosulfonamides. The 6 alpha -fluorpregnanes (I) are intermediates for the synthesis of steroids useful as anti-inflammatory and anti-asthmatic agents.

    专利号:WO-2022035917-A1
    优先权日:2020-08-14
    标题:Synthesis of fluorinated nucleotides

    专利号:WO-2022232500-A1
    优先权日:2021-04-30
    标题:Synthesis of sulfonyl halide terminated polyethylene
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    合成参考文献


    摘要:McMurtrey, K. B.; Sanford, M. S., Science of Synthesis: Cross Coupling and Heck-Type Reactions, (2012) 2, 558.
    摘要:van der Puyl, V.; Shenvi, R. A., Science of Synthesis: Base-Metal Catalysis, (2023) 2, 639.
    摘要:Wang, X.; Hu, J., Science of Synthesis: Modern Strategies in Organofluorine Chemistry, (2025) 2.
    摘要:Ruskin, J.; Lectka, T., Science of Synthesis: Modern Strategies in Organofluorine Chemistry, (2025) 2.
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