CAS: 1122-74-3; 4-Iodo-2-Methylsulfanylpyrimidine

该化合物是一种七环有机化合物,其特征是4号位置用火利米丁环替换碘原子,2号位置用甲基硫基组,该化合物一般是固体,因其在医药化学中的潜在应用而闻名,特别是因其与生物目标相互作用的能力而在药品开发中的潜在应用;碘原子的存在可增强化合物的再活性和脂性,而甲基硫基组可能影响其电子特性和溶性. 4-Iodo-2-(甲基硫基)可以参与各种化学反应,包括核生殖器替代和联动反应,使其成为有机合成中有价值的中间体.其分子结构有助于其独特的化学行为,并且经常被研究其在复杂分子合成中的作用.与许多卤化化合物一样,在处理该物质时,由于潜在的毒性和环境影响,应采取安全防范措施.

结构式图片

相似化合物

1333077-61-4 2648368-66-3 107403-27-0

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上下游产品

4-Chloro-2-methylthiopyrimidine 2-(methylsulfanyl)pyrimidine 2-(methylsulfanyl)pyrimidine 2-(methylthio)-4-(tributylstannyl)pyrimidine 2-(methylthio)-4-(trifluoromethyl)pyrimidine 4-iodo-6-methyl-2-methylsulfanyl-pyrimidine

合成工艺路线路线简述

    📜2-甲硫基嘧啶置于四甲基乙二胺,Zinc(II) Chloride,碘体系中,用 四氢呋喃 用作溶剂,化学反应 2.0H,以77%的收率获得4-碘-2-甲基磺酰基嘧啶
    参考文献:Azine And Diazine Functionalization Using 2,2,6,6-Tetramethylpiperidino-Based Lithium-metal Combinations: Application To The Synthesis Of 5,9-Disubstituted Pyrido[3',2':4,5]Pyrrolo[1,2-C]Pyrimidines
    标题:Azine And Diazine Functionalization Using 2,2,6,6-Tetramethylpiperidino-Based Lithium-metal Combinations: Application To The Synthesis Of 5,9-Disubstituted Pyrido[3',2':4,5]Pyrrolo[1,2-C]Pyrimidines
    摘要:The Synthesis Of Triaryl Methanols Was Investigated By Reacting Different 4-Metalated 2-Substituted Pyrimidines With Diaryl Ketones,The Latter Being Generated By Deprotocupration-Aroylation Of Azine And Diazine Substrates. Cyclization Of The Triaryl Methanols Thus Obtained Afforded Pyrido[3,2:4,5]Pyrrolo[1,2-C]Pyrimidines,Which Were Evaluated For Kinase Inhibition And Antiproliferative Activities In Melanoma Cells.
    Doi:10.1055/s-0035-1560496

    海关参考信息

    专利信息


    专利号:US-6784190-B2
    优先权日:1997-12-17
    标 题 :Integrin receptor antagonists
    发明人:ASKEW BEN C; COLEMAN PAUL J; DUGGAN MARK E; HALCZENKO WASYL; HARTMAN GEORGE D; HUNT CECILIA A; HUTCHINSON JOHN H; MEISSNER ROBERT S; PATANE MICHAEL A; SMITH GARRY R; WANG JIABING
    权利人:MERCK & CO INC
    摘要:The present invention relates to compounds and derivatives thereof, their synthesis, and their use as integrin receptor antagonists. More particularly, the compounds of the present invention are antagonists of the integrin receptors alphavbeta3, alphavbeta5, and/or alphavbeta6 and are useful for inhibiting bone resorption, treating and preventing osteoporosis, and inhibiting vascular restenosis, diabetic retinopathy, macular degeneration, angiogenesis, atherosclerosis, inflammation, wound healing, viral disease, tumor growth, and metastasis.

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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, 390.
    摘要:von Angerer, S., Science of Synthesis Knowledge Updates, (2011) 1, 311.
    摘要:von Angerer, S., Science of Synthesis Knowledge Updates, (2011) 1, 360.
    摘要:von Angerer, S., Science of Synthesis Knowledge Updates, (2011) 1, 356.
    摘要:von Angerer, S., Science of Synthesis Knowledge Updates, (2011) 1, 394.
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