CAS: 5053-43-0; 2-Methylpyrimidine

该化合物是一种具有分子式C5H6N2的七环有机化合物,其分子式为C5H6N2,其2位置为以甲基组替代的火利米丁环,由于其反应性火利米丁核心,该化合物是制药和农用化学合成的多用途中间体,其结构特性使得能够应用开发活性成分,包括抗病毒和抗硫剂.该甲基组增强了稳定性,调节电子效应,促进了选择性功能化. 2-甲基丙烯胺的特点是其高纯度和在诸如藻类,细胞化和核生殖器替代等反应中的一贯性能,在建立复杂的分子框架时,在研究和工业环境中通常使用该化合物的可靠性.

结构式图片

相似化合物

37972-24-0 14080-23-0 22868-76-4

欧盟法规

ECHA物质C&L通报

上下游产品

4-chloro-2-methylpyrimidine 2,4-dichloro-2-methylpyrimidine malonaldehydebis(dimethylacetal) acetamidine hydr°Chloride 2-(β-styryl)pyrimidine ethyl 2-oxo-3-(pyrimidin-2-yl)propanoate 2-methyl-1,4,5,6-tetrahydropyrimidine 2-methylpyrimidine 1-oxide

合成工艺路线路线简述

    2-甲基-1,4,5,6-四氢嘧啶置于palladium/alumina体系中,化学反应生成 2-甲基嘧啶
    参考文献:The Spectroscopic And Photophysical Effects Of The Position Of Methyl Substitution. Ii. 2‐methylpyrimidine
    标题:The Spectroscopic And Photophysical Effects Of The Position Of Methyl Substitution. Ii. 2‐methylpyrimidine
    摘要:Laser-Induced Fluorescence Excitation And Dispersed Fluorescence Spectra Of The First N-π* Transition Of Jet-Cooled 2-Methylpyrimidine Have Been Recorded And Analyzed. This Work Extends Our Earlier Study Of The Spectroscopic And Photophysical Effects Of Methyl Substitution In 4-And 5-Methylpyrimidine. An Unusual Fermi Resonance Involving The 6An0 Progression Forms The Focus Of The Present Study. The 6A10 Vibronic Transition Is Observed To Be Split Into A Triad Of Transitions. Dispersed Fluorescence Spectra Are Used To Identify The Dark Background State Responsible For The Fermi Resonance Coupling As The 16B1(3A''2) Vibration/internal Rotation Combination Level. This Level Is Selectively Coupled By Symmetry Constraints To 6A1(0A1),Leaving The 6A1(1E'') Level Unperturbed. The Positions And Intensities Of The Triad Of Peaks In The Excitation Spectrum Allow A Quantitative Determination Of The 6A1(0A'1)↔16B1(3A2) Coupling Matrix Element Of V=4.1 Cm−1. This Vibration/internal Rotation Fermi Resonance Is Thus Typical Of The New Types Of Routes To Vibrational State Mixing Which Are Opened By Methyl Substitution. Higher Members Of The 6An0 Progression Are Also Involved In Fermi Resonance Mixing. However,In Addition,These Levels Experience Weaker,Less State-Specific Coupling To A Bath Of Same-Symmetry States At That Energy. The Excitation Spectrum Provides An Estimate Of The Average Coupling Matrix Element Of This Second Tier Coupling Of ∼1 Cm−1.
    DOI:10.1063/1.462121

    专利信息


    专利号:US-9755163-B2
    优先权日:2010-04-30
    标 题:Synthesis of four coordinated palladium complexes and their applications in light emitting devices thereof
    发明人:LI JIAN; TURNER ERIC
    权利人:ARIZONA BOARD OF REGENTS ACTING FOR AND ON BEHALF OF ARIZONA STATE UNIV; ARIZONA BOARD OF REGENTS ACTING FOR OR ON BEHALF OF ARIZONA STATE UNIV
    摘要:Synthesis of four coordinated palladium complexes and their applications in light emitting devices thereof.

    专利号:US-9126995-B2
    优先权日:2011-11-08
    标题:Method for catalytic asymmetric synthesis of optically active isoxazoline compound and optically active isoxazoline compound
    发明人:TOYAMA KEN-ICHI; MORIYAMA YUJI; MATOBA KAZUTAKA; YAOSAKA MANABU; IKEDA EITATSU
    权利人:NISSAN CHEMICAL IND LTD
    摘要:There is provided a method for catalytic asymmetric synthesis of optically active isoxazoline compound and an optically active isoxazoline compound. A method for catalytic asymmetric synthesis of optically active isoxazoline compound of a formula (6) including reacting an α,β-unsaturated carbonyl compound of a formula (1) and a hydroxylamine in a solvent in the presence of a base by adding a chiral phase transfer catalyst. An optically active isoxazoline compound of a formula (13) that can be synthesized by the method.

    专利号:WO-2024137329-A1
    优先权日:2022-12-20
    标 题:Methods for the synthesis of complement factor d inhibitors and intermediates thereof
    发明人:HASHIMOTO AKIHIRO; TIPPARAJU SURESH KUMAR
    权利人:ALEXION PHARMA INC
    摘要:The present disclosure provides methods for the synthesis of complement factor D inhibitors and intermediates thereof.

    专利号:US-9324957-B2
    优先权日:2010-04-30
    标 题:Synthesis of four coordinated gold complexes and their applications in light emitting devices thereof
    发明人:LI JIAN; TUMER ERIC
    权利人:LI JIAN; TUMER ERIC; UNIV ARIZONA STATE
    摘要:Synthesis of four coordinated gold complexes and their applications in light emitting devices thereof.

    专利号:WO-2021126118-A1
    优先权日:2019-12-20
    标 题:Synthesis of 2-(substitutedphenyl)-5-(substitutedheteroaryl)- 1h-benzimidazole derivatives and investigation of their biological effects
    发明人:KAPLANCIKLI ZAFER ASIM; ÖZKAY YUSUF; ACAR ÇEVİK ULVIYE; SAÄžLIK BEGÜM NURPELIN; OSMANİYE DERYA; LEVENT SERKAN; KAYA ÇAVUÅžOÄžLU BETÜL; ATLI EKLİOÄžLU ÖZLEM; KARADUMAN ABDULLAH BURAK
    权利人:ANADOLU UENIVERSITESI
    摘要:The invention is related to the synthesis of 2-((5-(2-(4-Substitutedphenyl)-1H-benzo[d]imidazole-6-yl)-1,3,4-oxadiazole-2-yl)thio)-1-(4substitutedpiperazine-1-yl)-ethane-1-one derivative compounds and investigation of their biological effects. Cytotoxicity of the obtained compounds on 5 different cancer cell lines was evaluated and their selectivity indices were calculated.

    专利号:US-9982005-B2
    优先权日:2013-04-04
    标 题 :Macrolides and methods of their preparation and use
    发明人:MYERS ANDREW G; SEIPLE IAN BASS; ZHANG ZIYANG
    权利人:HARVARD COLLEGE
    摘要:Provided herein are methods of preparing macrolides by the coupling of an eastern and western half, followed by macrocyclization, to provide macrolides, including both known and novel macrolides. Intermediates in the synthesis of macrolides including the eastern and western halves are also provided. Pharmaceutical compositions and methods of treating infectious diseases and inflammatory conditions using the inventive macrolides are also provided. A general diastereoselective aldol methodology used in the synthesis of the western half is further provided.
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    合成参考文献


    摘要:von Angerer, S., Science of Synthesis Knowledge Updates, (2011) 1, 353.
    摘要:von Angerer, S., Science of Synthesis Knowledge Updates, (2011) 1, 447.
    摘要:von Angerer, S., Science of Synthesis Knowledge Updates, (2011) 1, 445.
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