CAS: 156-81-0; Pyrimidine-2,4-Diamine

该化合物是一种有机化合物,其特点是其火水环结构,在2和4个位置上有两个氨基组,该化合物一般是白到白的晶状固体,在水和各种有机溶剂中可溶解,其分子式为C4H6N4,其分子重量相对较低. 2,4-Diminopyrimidine因其在合成药物和农用化学化学品,特别是在研制抗氟酸药物方面作为中间体的作用而著称.氨基氨基胺团体的存在使它成为有机合成的多用途建筑块,允许进行各种化学修改.此外,它展示了生物活动,导致其在药用化学方面进行调查.安全数据表明,应当谨慎地处理,因为它在接触时可能会对健康造成危害.

结构式图片

相似化合物

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CAS号1004-01-9 5-溴嘧啶-2,4-二胺 | CAS号73183-34-3 双戊酰二硼 | CAS号58243-08-6 反式-3-乙氧基丙烯腈 | CAS号50-01-1 盐酸胍 | CAS号3993-78-0 2-氨基-4-氯嘧啶 | CAS号2032-34-0 氰基乙醛缩二乙醇 | CAS号3934-20-1 2,4-二氯嘧啶 | CAS号156-83-2 2,4-二氨基-6-氯嘧啶 | CAS号14001-63-9 4-甲基-2-甲硫基嘧啶 | CAS号15640-40-1 Phenol,4,4'-met... | CAS号74638-76-9 2,4-二氨基嘧啶-3-氧化物 | CAS号462651-80-5 7-氨基咪唑并[1,2-A]嘧啶 | CAS号591227-12-2 2-phenylimidazo...

合成工艺路线路线简述

    2,4-二氨基-6-氯嘧啶置于溶剂黄146,锌体系中,化学反应生成2,4-二氨基嘧啶
    参考文献:Buettner,Chemische Berichte,1903,Vol. 36,P. 2234
    标题:Buettner,Chemische Berichte,1903,Vol. 36,P. 2234

    专利信息


    专利号:WO-2025101716-A1
    优先权日:2023-11-07
    标题:Processes for synthesis of trifunctionalized sulfur(vi) compounds
    发明人:LOPCHUK JUSTIN; SHULTZ ZACHARY; ATHAWALE PARESH
    权利人:H LEE MOFFITT CANCER CT & RES
    摘要:This disclosure describes processes for the asymmetric synthesis of trifunctionalized sulfur(VI) containing organic compounds of Formula I and Formula VI, as well as compounds of Formula I and Formula VI prepared by the processes described.

    专利号:US-2023220434-A1
    优先权日:2020-01-09
    标 题 :Composistions and methods for crispr enabled dna synthesis
    发明人:LYNCH MICHAEL DAVID; MOREB EIRIK ADIM; YANG TIAN
    权利人:UNIV DUKE
    摘要:Methods for CRISPR Enabled DNA Synthesis and compositions arising from the methods are provided. The methods may include ligation of partially single stranded DNA donor and acceptor oligonucleotides that are covalently linked to a subsequence of the target DNA to be sequenced followed by cleavage of the ligated product. In this manner the donor and acceptor oligonucleotides shuttle a growing subsequence of the target DNA with each cycle. A mutant Cpfl nuclease is missing non-specific ssDNA nuclease activity may be used for cleavage of the ligation product. Fourteen ligation/cleavage cycles can result in synthesis of ssDNA of greater than 10,000 bp in length.

    专利号:US-8825411-B2
    优先权日:2004-05-04
    标 题:Design, synthesis and assembly of synthetic nucleic acids
    发明人:GOVINDARAJAN SRIDHAR; MINSHULL JEREMY S; NESS JON E
    权利人:GOVINDARAJAN SRIDHAR; MINSHULL JEREMY S; NESS JON E; DNA TWOPOINTO INC
    摘要:Methods of synthesizing oligonucleotides with high coupling efficiency (>99.5%) are provided. Methods for purification of synthetic oligonucleotides are also provided. Instrumentation configurations for oligonucleotide synthesis are also provided. Methods of designing and synthesizing polynucleotides are also provided. Polynucleotide design is optimized for subsequent assembly from shorter oligonucleotides. Modifications of phosphoramidite chemistry to improve the subsequent assembly of polynucleotides are provided. The design process also incorporates codon biases into polynucleotides that favor expression in defined hosts. Design and assembly methods are also provided for the efficient synthesis of sets of polynucleotide variants. Software to automate the design and assembly process is also provided.

    专利号:US-7105666-B2
    优先权日:2002-06-27
    标 题:Synthesis of purine derivatives
    发明人:HAMMARSTROEM LARS G J; KRAUSS NANCY ELISABTH; LABADIE SHARADA SHENVI; SMITH DAVID BERNARD; TALAMAS FRANCISCO XAVIER
    权利人:ROCHE PALO ALTO LLC
    摘要:The present invention provides a method for producing 2-, 6-, 8- and 9-substituted purine compounds from 4,6-dihalo-5-nitro-2-alkyl-pyrimidine compounds in solution or by solid phase techniques. The present process provides for the sequential introduction of amine substituents at the 4- and 6-positions, displacement of an alkylsulfony group at the 2-position of the pyrimidine, reduction of the nitro group and formation of the imidazole portion of the purine compound. Furthermore, the methods of the present invention are ideally suited to the preparation of a library of purine compounds.

    专利号:US-7256197-B2
    优先权日:2001-10-12
    标 题 :Methods for synthesis of diarylmethanes
    发明人:ROSOWSKY ANDRE; CHEN HAN
    权利人:DANA FARBER CANCER INST INC
    摘要:The present invention relates to dihydrofolate reductase inhibitors having an aromatic group and a heteroaromatic group linked by a methylene group; methods of preparation of dihydrofolate reductase inhibitors that include metal mediated cross coupling of an aromatic halide or heteroaromatic halide with an organozinc reagent; and methods of treatment and pharmaceutical compositions that utilize or comprise one or more of such dihydrofolate reductase inhibitors.

    专利号:US-6232462-B1
    优先权日:1994-08-30
    标题:Reduction of nonspecific hybridization by using novel base-pairing schemes
    发明人:COLLINS MARK L; HORN THOMAS; SHERIDAN PATRICK J; WARNER BRIAN D; URDEA MICHAEL S
    权利人:BAYER AG
    摘要:Methods are provided for substantially reducing background signals encountered in nucleic acid hybridization assays. The method is premised on the elimination or significant reduction of the phenomenon of nonspecific hybridization, so as to provide a detectable signal which is produced only in the presence the target polynucleotide of interest. In addition, a novel method for the chemical synthesis of isoguanosine or 2′-deoxy-isoguanosine is provided. The invention also has applications in antisense and aptamer therapeutics and drug discovery.
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    主要参考文献

    [参考文献]: Brian D Herman, Et Al. The Acyclic 2,4-Diaminopyrimidine Nucleoside Phosphonate Acts As A Purine Mimetic In Hiv-1 Reverse Transcriptase Dna Polymerization. J Biol Chem. 2010 Apr 16;285(16):12101-8.
    [参考文献]: Fatima Tamtam, Et Al. Ultra Performance Liquid Chromatography Tandem Mass Spectrometry Performance Evaluation For Analysis Of Antibiotics In Natural Waters. Anal Bioanal Chem. 2009 Mar;393(6-7):1709-18.
    [参考文献]: Ilya Lebeau, Et Al. Inhibitory Activities Of Three Classes Of Acyclic Nucleoside Phosphonates Against Murine Polyomavirus And Primate Simian Virus 40 Strains. Antimicrob Agents Chemother. 2007 Jun;51(6):2268-73.
    [参考文献]: Luke Mercer, Et Al. 2,4-Diaminopyrimidines As Potent Inhibitors Of Trypanosoma Brucei And Identification Of Molecular Targets By A Chemical Proteomics Approach. Plos Negl Trop Dis. 2011 Feb 8;5(2):E956.
    [参考文献]: Mary J Carroll, Et Al. Evidence For Dynamics In Proteins As A Mechanism For Ligand Dissociation. Nat Chem Biol. 2012 Jan 15;8(3):246-52.

    合成参考文献


    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, 323.
    摘要:B. Roth and J.Z. Strelitz. J. Org. Chem. 34, 821 (1969).
    摘要:G.B. Barlin and W. Pfleiderer. J. Chem. Soc., B 1971.
    参考文献:10.4315/0362-028x-65.4.688
    摘要:Gong PS, Jeng SL, Hsu YF, Lin CC, Lin SY. Development of a method for the determination of pyrimethamine concentrations in feeds by ion-pairing high-performance liquid chromatography. J Food Prot. 2002 Apr;65(4):688–91. doi: 10.4315/0362-028x-65.4.688.
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