CAS: 16357-69-0; 4-Aminopyrimidine-5-Carbonitrile

该化合物是一种七环有机化合物,其成分包括氨基氨基和环氨基亚的功能组群,其成分在湿米地骨上,这种结构使它成为制药和农用化学合成的多功能中间体,特别是用于开发活性成分.它的活性场所可以进行选择性的修改,方便复杂分子的构造.该化合物的高度纯度和稳定性确保核生殖替代和凝聚反应的可靠性能.它通常用于为医药化学应用,包括活性酶抑制剂和抗病毒剂,而基于比利米丁的肉类的肉食动物的准备中.它具有明确界定的化学特性,并且与各种反应条件相容,因此它成为研究和工业环境中的宝贵建筑.

结构式图片

相似化合物

20737-41-1 16357-83-8 109831-70-1

欧盟法规

ECHA物质C&L通报

上下游产品

thi°Carboxamide sodium ethanolate aminomethylene-malononitrile ethanol 4-aminopyrimido(5,5-d)pyrimidine 4-Amino-5-aminomethyl-pyrimidin 4-amino-pyrimidin-5-carboxylic acid 4-aminopyrimidine-5-carbothioamide

合成工艺路线路线简述

    📜3-Cyanamino-2-Cyanopropenenitrile Sodium Salt置于5% Pd On Active Carbon 盐酸,氢气,三乙胺体系中,用 甲醇 用作溶剂,25.0 °C,206.84 Kpa 条件下,反应 3.83H,反应生成4-氨基嘧啶-5-甲腈
    参考文献:Schmidt,Hans-Werner; Koitz,Gerald; Junek,Hans,Journal Of Heterocyclic Chemistry,1987,Vol. 24,P. 1305-1307
    标题:Schmidt,Hans-Werner; Koitz,Gerald; Junek,Hans,Journal Of Heterocyclic Chemistry,1987,Vol. 24,P. 1305-1307

    海关参考信息

    专利信息


    专利号:WO-2011116933-A1
    优先权日:2010-03-24
    标 题 :Process for the preparation of 2-substituted 4-amino-5-cyanopyrimidines
    发明人:DICK VIKTOR; HANSELMANN PAUL; KRAMER RAINER; LADNAK VIKTOR
    权利人:LONZA AG; DICK VIKTOR; HANSELMANN PAUL; KRAMER RAINER; LADNAK VIKTOR
    摘要:A compound of the formula (I), wherein R 1 is C 1-4 alkyl or phenyl, is prepared by reacting a dicyanomethanide of the formula: M r n + [CH(CN) 2 ] rÌ… n (II), wherein M is an alkali or alkaline earth metal and r is 1 or 2, with carbon monoxide to obtain a dicyanoethenolate of the formula: M r n + [(NC) 2 C=CH–O] rÌ… (III), which is acylated to obtain an acyloxymethylenemalononitrile of the formula: (NC) 2 C=CH–OCOR 2 (IV), wherein R 2 is C 1-4 alkyl, which in turn is reacted with an amidine of the formula (V) to obtain the 4-amino-5-cyanopyrimidine of the formula (I). The compound of formula (I), wherein R is methyl, is an intermediate in a synthesis of thiamin (vitamin B 1 ).

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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


    摘要:von Angerer, S., Science of Synthesis Knowledge Updates, (2011) 1, 133.
    摘要:von Angerer, S., Science of Synthesis Knowledge Updates, (2011) 1, 296.
    摘要:D.J. Brown and M.N. Padden-Row. J. Chem. Soc., C 1966, 164.
    参考文献:10.1021/acsinfecdis.1c00432
    摘要:Charoensutthivarakul S, Thomas SE, Curran A, Brown KP, Belardinelli JM, Whitehouse AJ, Acebrón-García-de-Eulate M, Sangan J, Gramani SG, Jackson M, Mendes V, Floto RA, Blundell TL, Coyne AG, Abell C. Development of Inhibitors of SAICAR Synthetase (PurC) from Mycobacterium abscessus Using a Fragment-Based Approach. ACS Infect. Dis. 2022 Jan 17;8(2):296–309. doi: 10.1021/acsinfecdis.1c00432.
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