CAS: 41995-30-6; 3,5-Dimethylpyridin-2-Amine

该化合物是环3和5个位置上的氨基有机化合物,在2个位置和甲基替代组群的甲状腺素环3和5个位置上形成一个氨基有机化合物.这种结构具有独特的反应性,使它在制药和农用化学合成中成为有价值的中间体.其电子丰富的基有利于核生殖替代和金属催化联动反应,从而能够制造复杂的分子.该化合物的高度纯度和稳定性确保了在诸如离心设计和活性药物成分开发等应用方面的一致性能.其定义明确的晶体形式可以精确处理和储存,并符合严格的工业标准.

结构式图片

相似化合物

1603-40-3 183428-91-3 863479-77-0

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上下游产品

CAS号92992-85-3 2-溴-3,5-二甲基吡啶 | CAS号591-22-0 3,5-二甲基吡啶 | CAS号3718-65-8 3,5-二甲基吡啶N-氧化物

合成工艺路线路线简述

    📜3,5-二甲基吡啶置于sodium Amide体系中,用 Various Solvent(S) 作为反应溶剂,以36%的收率获得产物3,5-二甲基吡啶-2-胺
    参考文献:Siegl,Walter O.,Journal Of Heterocyclic Chemistry,1981,Vol. 18,P. 1613-1618
    标题:Siegl,Walter O.,Journal Of Heterocyclic Chemistry,1981,Vol. 18,P. 1613-1618

    海关参考信息

    专利信息


    专利号:US-2023303611-A1
    优先权日:2022-01-21
    标题:Synthesis of an antiviral azasugar triphosphate
    发明人:KOTIAN PRAVIN L; Dang zhao; WU MINWAN
    权利人:BIOCRYST PHARM INC
    摘要:Provided are methods of making the active 5′-triphosphate form of galidesivir (compound 1) and the active 5′-triphosphate form of azasugar nucleoside analogues (compound 2):a potent anti-viral compound useful for broad spectrum treatment, suppression, and prevention of viral infections. The syntheses of compound 1 and compound 2 can be achieved via selective formation of protected intermediate 1b and protected intermediate 2b, respectively:

    专利号:US-7772246-B2
    优先权日:2007-08-01
    标题:Pyrazole compounds as RAF inhibitors
    发明人:CUI JINGRONG JEAN; DEAL JUDITH GAIL; GU DANLIN; GUO CHUANGXING; JOHNSON MARY CATHERINE; KANIA ROBERT STEVEN; KEPHART SUSAN ELIZABETH; LINTON MARIA ANGELICA; MCALPINE INDRAWAN JAMES; PAIRISH MASON ALAN; PALMER CYNTHIA LOUISE
    权利人:PFIZER
    摘要:The present invention is directed to compounds of Formula (I), n nand to pharmaceutically acceptable salts thereof, their synthesis, and their use as Raf inhibitors.

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    📌 第三方产品分析报告

    ✅ COA系统入驻 | 共享模式

    合成参考文献


    参考文献:10.1016/s0960-894x(00)00389-9
    摘要:Hagmann WK, Caldwell CG, Chen P, Durette PL, Esser CK, Lanza TJ, Kopka IE, Guthikonda R, Shah SK, MacCoss M, Chabin RM, Fletcher D, Grant SK, Green BG, Humes JL, Kelly TM, Luell S, Meurer R, Moore V, Pacholok SG, Pavia T, Williams HR, Wong KK. Substituted 2-aminopyridines as inhibitors of nitric oxide synthases. Bioorganic & Medicinal Chemistry Letters. 2000 Sep;10(17):1975–8. doi: 10.1016/s0960-894x(00)00389-9.
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