CAS: 38240-21-0; 3-Aminopyridine-2(1H)-Thione

该化合物是有机化合物,其特点是其环结构,代之以氨基环形结构,与氨基基环状和硫磷功能组相替代,该化合物通常具有氮和含硫乙烯环状物的特性,在室温下是一种黄到褐的固体,由于氨基组的存在,可以从事氢结合,因此溶于水和酒精等极溶剂中,该产品具有溶解性,硫化物组有助于其再活动,使其得以参与各种化学反应,包括核细胞代用品和与金属离子的协调.3-亚敏性丙胺-2(1H)-硫磷也可能展示生物活动,使之对医药化学和药理具有兴趣,分子结构允许在制药,农用化学品以及协调化学中的潜在应用.应当参考安全数据,以便处理和储存,与任何化学物质一样,确保采取适当的预防措施.

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合成工艺路线路线简述

    📜3-硝基-2-吡啶硫醇置于盐酸,Tin(Ll) Chloride体系中,化学反应生成2-巯基-3-氨基吡啶
    参考文献:Takahashi; Maki,Yakugaku Zasshi/journal Of The Pharmaceutical Society Of Japan,1958,Vol. 78,P. 417,420
    标题:Takahashi; Maki,Yakugaku Zasshi/journal Of The Pharmaceutical Society Of Japan,1958,Vol. 78,P. 417,420

    海关参考信息

    专利信息


    专利号:US-4171438-A
    优先权日:1975-07-23
    标 题:0-2-Isocephem-4-carboxylic acid derivatives as antibacterial agents
    发明人:DOUGLAS JAMES L; HORNING DONALD E; MORRIS LEESON R
    权利人:BRISTOL MYERS CO
    摘要:There is described the stereoselective total synthesis of novel DELTA 2,3-1,4-morpholine-2-carboxylic acids possessing a fused beta -lactam ring in the 1,6-position and carrying a substituent cis to carbon 5 in the 7-position of the fused ring system represented by the general formula I wherein X is acylamino and Z represents optionally substituted C1-C6 alkyl, aryl or aralkyl. Also included in the invention are compounds of the above formula in which the carboxyl group at the 2-position is protected as by an easily cleavable ester group and salts of both the free acids and carboxyl-protected compounds. The compounds are potent antibacterial agents.

    专利号:US-4118566-A
    优先权日:1975-07-23
    标 题:Δ2,3 -1,4-Morpholine-2-carboxylic acid derivatives as antibacterial agents
    发明人:HORNING DONALD E; MORRIS LEESON R; DOUGLAS JAMES L
    权利人:BRISTOL MYERS CO
    摘要:There is described the stereoselective total synthesis of novel DELTA 2,3-1,4-morpholine-2-carboxylic acids possessing a fused beta -lactam ring in the 1,6-position and carrying a substituent cis to carbon 5 in the 7-position of the fused ring system represented by the general formula I wherein X is amino, azido or acylamido and Z represents optionally substituted C1-C6 alkyl, aryl, aralkyl or heterocyclic. Also included in the invention are compounds of formula I in which the carboxyl group at the 2-position is protected as by an easily cleavable ester group and salts of both the free acids and carboxyl-protected compounds of formula I. The compounds of formula I are potent antibacterial agents or are of use as intermediates in the preparation of such antibacterial agents.

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    合成参考文献


    摘要:Ulrich, H., Science of Synthesis, (2002) 11, 841.
    摘要:Ulrich, H., Science of Synthesis, (2004) 17, 192.
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