CAS: 54585-47-6; 4,6-Dimethyl-2-Thioxo-1,2-Dihydropyridine-3-Carbonitrile

该化合物是一种七环有机化合物,以甲型,硫基和硝基功能组取代了核心,其分子结构的特点是存在电脱钩和电饱和组,使其成为有机合成的多功能中间体,特别是在制药和农用化学制剂的制作方面.该化合物的再活性通过硫醇组得到增强,为建造含硫衍生物提供了选择性的修改.该化合物在标准条件下的稳定性和高纯度使其适合于精确的合成应用.研究人员认为该化合物在开发生物活性分子(包括潜在的治疗剂和催化性树脂)方面的作用是其具有价值的.

结构式图片

欧盟法规

C&L通报

上下游产品

CAS号7357-70-2 2-氰基硫代乙酰胺 | CAS号123-54-6 乙酰丙酮 | CAS号6623-21-8 4,6-二甲基烟腈 | CAS号5875-28-5 Thi°Cyanic acid... | CAS号129224-51-7 2-氰基-2-环亚戊基乙烷硫代酰胺 | CAS号129224-53-9 2-cyano-2-cyclo... | CAS号63913-42-8 (E)-4-morpholin... | CAS号52505-42-7 1-(3-氨基-4,6-二甲基... | CAS号58327-76-7 3-氨基-4,6-二甲基噻吩并... | CAS号41601-44-9 4,6-二甲基-3-氨基吡唑并... | CAS号128918-28-5 3-氨基-4,6-二甲基噻吩[... | CAS号128918-14-9 2-[(3-amino-4,6... | CAS号52505-56-3 Thieno[2,3-b]py... | CAS号14237-71-9 2-氯-3-氰基-4,6-二甲基吡啶 | CAS号72456-86-1 4,6-dimethyl-2-... | CAS号67795-42-0 3-氨基-4,6-二甲基噻吩[... | CAS号835626-21-6 (3-azido-4,6-di...

合成工艺路线路线简述

    📜2-氯-3-氰基-4,6-二甲基吡啶置于硫脲体系中,用 乙醇 作为反应溶剂,以83 %的收率获得产物3-氰基-4,6-二甲基-2-硫基吡啶
    参考文献:通过砜的配体偶联反应进行 N-杂芳族氟烷基化
    标题:通过砜的配体偶联反应进行 N-杂芳族氟烷基化
    摘要:通过格氏试剂促进的形式so 2挤出反应,由氟烷基2-氮杂杂芳基砜有效合成氟烷基化n-杂芳烃.该反应通过五配位硫(Vi)中间体的配体偶联进行,并表现出独特的氟效应.
    DOI:10.1002/anie.202401091

    海关参考信息

    专利信息


    专利号:US-6531470-B1
    优先权日:1998-01-23
    标题:Oxazolidinone combinatorial libraries, compositions and methods of preparation
    发明人:GORDEEV MIKHAIL F; LUEHR GARY W; PATEL DINESH V; NI ZHI-JIE; GORDON ERIC
    权利人:UPJOHN CO
    摘要:Oxazolidinones and methods for their synthesis are provided. Also provided are combinatorial libraries comprising oxazolidinones, and methods to prepare the libraries. Further provided are methods of making biologically active oxazolidinones as well as pharmaceutically acceptable compositions comprising the oxazolidinones. The methods of library preparation include the attachment of oxazolidinones to a solid support. The methods of compound preparation in one embodiment involve the reaction of an iminophosphorane with a carbonyl containing polymeric support.

    专利号:CN-111699248-A
    优先权日:2018-01-31
    标题:Biocatalysts and methods for the synthesis of mixed disulfide conjugates of thienopyridine compounds

    专利号:US-12188069-B2
    优先权日:2018-01-31
    标 题 :Biocatalyst and methods for synthesizing mixed disulfide conjugates of thienopyridine compounds
    发明人:ZHANG HAOMING
    权利人:UNIV MICHIGAN REGENTS
    摘要:The present invention relates to methods for synthesizing mixed disulfide conjugates of thienopyridine compounds with a genetically engineered variant of cytochrome P450 BM3 or CYP102A1 as a catalyst, and belongs to the field of chemical synthesis.

    专利号:US-6562844-B2
    优先权日:1998-01-23
    标 题:Oxazolidinone combinatorial libraries, compositions and methods of preparation
    发明人:GORDEEV MIKHAIL F; LUEHR GARY W; PATEL DINESH V; NI ZHI-JIE; GORDON ERIC
    权利人:UPJOHN CO
    摘要:Oxazolidinones and methods for their synthesis are provided. Also provided are combinatorial libraries comprising oxazolidinones, and methods to prepare the libraries. Further provided are methods of making biologically active oxazolidinones as well as pharmaceutically acceptable compositions comprising the oxazolidinones. The methods of library preparation include the attachment of oxazolidinones to a solid support. The methods of compound preparation in one embodiment involve the reaction of an iminophosphorane with a carbonyl containing polymeric support.

    专利号:US-9056876-B2
    优先权日:2011-09-16
    标 题:Substituted 1H-pyrazolo[3′,4′,4,5]thieno[2,3-b]pyridin-3-amine analogs as positive allosteric modulators of the muscarinic acetylcholine receptor M4
    发明人:CONN JEFFREY P; LINDSLEY CRAIG W; WOOD MICHAEL R; HOPKINS COREY R; SALOVICH JAMES M; MELANCON BRUCE J
    权利人:UNIV VANDERBILT
    摘要:In one aspect, the invention relates to substituted 1H-pyrazolo[3′,4′:4,5]thieno[2,3-b]pyridin-3-amine analogs, derivatives thereof, and related compounds, which are useful as positive allosteric modulators of the muscarinic acetylcholine receptor M 4 (mAChR M 4 ); synthesis methods for making the compounds; pharmaceutical compositions comprising the compounds; and methods of treating neurological and psychiatric disorders associated with muscarinic acetylcholine receptor dysfunction using the compounds and compositions. This abstract is intended as a scanning tool for purposes of searching in the particular art and is not intended to be limiting of the present invention.

    专利号:US-7002020-B1
    优先权日:1998-01-23
    标题:Oxazolidinone combinatorial libraries, compositions and methods of preparation
    发明人:GORDEEV MIKHAIL F; LUEHR GARY W; PATEL DINESH V
    权利人:UPJOHN CO
    摘要:Oxazolidinones and methods for their synthesis are provided. Also provided are combinatorial libraries comprising oxazolidinones, and methods to prepare the libraries. Further provided are methods of making biologically active oxazolidinones as well as pharmaceutically acceptable compositions comprising the oxazolidinones. The methods of library preparation include the attachment of oxazolidinones to a solid support. The methods of compound preparation in one embodiment involve the reaction of an iminophosphorane with a carbonyl containing polymeric support.

    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

    合成参考文献


    摘要:Pharmaceutical Chemistry Journal, 19(313), 1985
    📝 需求与反馈
    尽可能描述清楚需求与问题信息
    ×

    通知