CAS: 3690-12-8; (4-Amino-2-Methoxypyrimidin-5-yl)Methanol

该化合物是有机化合物,其特点是其有糖浆环结构,即六人组成的芳香环,含有位于1号阵地和3号阵地的两个氮原子;该化合物的特点是一个氨基组(-NH2)和一个附属于此颗星环的甲氧基组 (-OCH3),以及一个水氧化硫组( - CH2OH),该组有助于其在极地溶剂中的再活性和溶性;该组通常是白色到白色的,从白到白的固体,由于存在极地功能组而溶于水和有机溶剂中;该复合体可能展示生物活动,使其对药物研究感兴趣,特别是针对各种疾病的药物研制具有兴趣;其特性,如熔点,沸点和特定的再活性,可因纯度和环境条件而不同而不同;与许多有机化合物一样,在处理时应采取安全防范措施,包括使用适当的个人防护设备.

结构式图片

上下游产品

4-氨基-2-甲氧基-5-嘧啶甲腈 4-Amino-2-Methoxy-Pyrimidine-5-Carbonitrile 6964-55-2
2-羟基-4-氨基-5-羟甲基嘧啶 5-Hydroxymethylcytosine 1123-95-1

合成工艺路线路线简述

    📜4-氨基-2-甲氧基-5-嘧啶甲腈置于palladium On Activated Charcoal 硫酸,氢气体系中,化学反应 3.0H,以53%的收率获得产物4-氨基-2-甲氧基-5-嘧啶甲醇
    参考文献:由氨基嘧啶甲醛合成吡啶并[2,3-D]嘧啶
    标题:由氨基嘧啶甲醛合成吡啶并[2,3-D]嘧啶
    摘要:2-甲氧基-4-氨基-5-Pyrimidinecarbaldehyde(2A),以及它的6-甲基2B和6-苯基衍生物2C中通过还原相应的aminopyrimidinecarbonitriles制备1.1A,1B的催化加氢得到5-羟甲基嘧啶3A,3B; N = 1.在相同条件下1C得到5-氨基甲基嘧啶4.2与带有-Ch 2 Co-部分的腈,酮和多官能羰基化合物缩合,得到吡啶并[2,3-D]嘧啶和嘧啶并-[4,5-B]喹啉衍生物.
    DOI:10.1002/jhet.5570350226

    海关参考信息

    专利信息


    专利号:WO-2022146324-A1
    优先权日:2020-12-29
    标 题 :Synthesis of pyrimidine-4(lh)-one derivatives from new hydrazineylidene
    发明人:SARIPINAR EMIN; BURCU HILAL JANSET; KEKEÇMUHAMMED HÜSEYIN; TAPERA MICHAEL
    权利人:T C ERCIYES UENIVERSITESI
    摘要:This invention relates to the synthesis of pyrimidine-4 (1H)-one derivatives from Meldrum's acid, carbonyl compounds (aldehyde/ketone), and guanylhydrazone derivatives and tautomers, enantiomers, and salts thereof.

    专利号:TR-2021011437-A2
    优先权日:2020-12-29
    标题 :SYNTHESIS OF PYRIMIDIN-4(1H)-ON DERIVATIVES FROM NEW HYDRAZINELIAN

    专利号:US-2009209554-A1
    优先权日:2004-03-24
    标题 :Thiazoliums as transketolase inhibitors
    发明人:BOYD STEVEN A; CONDROSKI KEVIN R; DE MEESE JASON; GONZALES STEPHEN S; GUNAWARDANA INDRANI W; KAPLAN TOMAS; HUEROU YVAN LE; LYSSIKATOS JOSEPH; ROMOFF TODD T; SULLIVAN FRANCIS X; THOMAS ALLEN
    权利人:ARRAY BIOPHARMA INC
    摘要:The present invention provides N-3′-pyridyl-methyl or N-2′-pyrazinylmethyl thiazolium derivatives of formula (I) which are useful as transketolase inhibitors wherein R 1 , R 2 , R 3 , Y, R 5 -R 9 , R a -R d , n and X − are as defined herein. The present invention also provides pharmaceutical compositions comprising the compounds of formula (I). The invention provides methods for inhibiting transketolase activity, reducing cellular ribose-5-phosphate levels, inhibiting nucleic acid synthesis, inhibiting cell proliferation and tumor cell growth in vitro and in vivo, stimulating apoptosis in tumor cells and treating cancer by administering a compound of formula (I) or a pharmaceutical composition thereof.

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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, 103.
    摘要:Journal of Antibiotics, Series A., 15(191), 1962
    参考文献:10.1016/s0960-894x(01)00373-0
    摘要:Reddick JJ, Saha S, Lee J, Melnick JS, Perkins J, Begley TP. The mechanism of action of bacimethrin, a naturally occurring thiamin antimetabolite. Bioorganic & Medicinal Chemistry Letters. 2001 Sep;11(17):2245–8. doi: 10.1016/s0960-894x(01)00373-0.
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