CAS: 153436-53-4; N-(3-Chlorophenyl)-6,7-Dimethoxyquinazolin-4-Amine

该化合物是一种化学化合物,其特点是五氯基核心结构,这是一种双环化合物,含有苯环,并附着于一个火林.这种具体的衍生物具有三氯基苯组和两个甲氧组,位于五氯基环的6和7个位置,有助于其独特的化学特性.氯原子的存在会加强其亲脂性,并可能影响其生物活动.甲氧基组可以参与氢结,影响化合物的溶性与再活动.这种化合物可能展示潜在的药理活动,使其对药用化学感兴趣.分子结构表明可能与生物目标发生相互作用,可以探索这些应用作为治疗用途.与许多五氯基苯基衍生物一样,可以对其在治疗各种疾病方面的作用进行调查,包括癌症和炎症.应当根据其化学性质来观察适当的处理和安全措施.

结构式图片

欧盟法规

ECHA物质C&L通报

上下游产品

ethyl 5-amino-1-phenyl-1H-pyrazole-4-carboxylate 4-chloro-1-(phenyl)-1H-pyrazolo[3,4-d]pyrimidine 3-chloro-aniline

合成工艺路线路线简述

    📜5-氨基-4-乙氧羰基-1-苯基吡唑置于三氯氧磷体系中,用 异丙醇 用作溶剂,化学反应 0.75H,反应生成4-(3-氯苯胺)-6,7-二甲氧基喹唑啉盐酸盐
    参考文献:Novel Dual Use Of Formamide-Pocl3 Mixture For The Efficient,One-Pot Synthesis Of Condensed 2H-Pyrimidin-4-Amine Libraries Under Microwave Irradiation
    标题:Novel Dual Use Of Formamide-Pocl3 Mixture For The Efficient,One-Pot Synthesis Of Condensed 2H-Pyrimidin-4-Amine Libraries Under Microwave Irradiation
    摘要:The Novel Dual Use Of Formamide-Pocl3 Mixture For The Incorporation Of A C-N Fragment To Form The Pyrimidine Nucleus And Its Subsequent Chlorination In An Efficient,One-Pot Synthesis Of Potentially Bioactive Condensed 2H-Pyrimidin-4-Amine Libraries Under Microwave Irradiation (Mwi) Is Reported. The One-Pot Microwave-Assisted Synthetic Protocol Is High-Yielding,Ecofriendly,Rapid,And Novel As Well As Eliminates Intermittent Work-Ups. The Protocol Can Be Adapted For The Library Synthesis Of Series Of A Condensed Pyrimidines.
    Doi:10.1080/00397911.2011.607934

    海关参考信息

    专利信息


    专利号:US-2025206743-A1
    优先权日:2022-03-25
    标 题:Tyk2 inhibitor synthesis and intermediates thereof
    发明人:MASSE CRAIG E; PHADKE AVINASH S; LAWSON JON P; LEVY STUART; YANG XIAOWEI; WU GUISHENG; FAN SHUFENG
    权利人:TAKEDA PHARMACEUTICALS CO
    摘要:Described herein are methods of synthesis of a tyrosine-protein kinase 2 (TYK2) inhibitor and to intermediate compounds of the synthesis and methods of making the intermediates. Also provided are pharmaceutically acceptable compositions including compounds prepared by the synthetic method and methods of treating disorders using the same.

    专利号:US-12060343-B2
    优先权日:2018-10-22
    标题 :Substituted 1,2,4-triazoles as intermediates in the synthesis of TYK2 inhibitors

    专利号:US-2023391751-A1
    优先权日:2018-10-22
    标题 :Substituted 1,2,4-triazoles as intermediates in the synthesis of tyk2 inhibitors

    专利号:US-11406709-B2
    优先权日:2014-09-15
    标 题 :Therapeutic and research application of PDCL3
    发明人:RAHIMI NADER
    权利人:UNIV BOSTON
    摘要:Described herein are novel compositions comprising, for example, PDCL3 polypeptides having VEGFR-2 inhibitory activity, inhibitory PDCL3 antibodies and PDCL3-binding fragments thereof, or PDCL3 inhibitory nucleic acid molecules, and methods of their use in anti-angiogenesis and anti-tumor proliferation and invasiveness therapies, such as the treatment of cancer, as well as the treatment of those vascular diseases where pathological angiogenesis plays a role, such as in carotid artery disease, macular degeneration, and plaque neovascularization. Also described herein are novel compositions comprising engineered PDCL3 polypeptides having enhanced chaperone activity, recombinant cells comprising such engineered PDCL3 polypeptides having enhanced chaperone activity, and methods thereof for therapeutic protein production and in vitro protein synthesis.

    专利号:BR-112015021965-B1
    优先权日:2013-03-13
    标题 :Pyrrolobenzodiazepine conjugates and compounds, pharmaceutical composition, use thereof for the treatment of a proliferative disease and method of synthesis of said compounds

    专利号:US-7052692-B1
    优先权日:1997-09-02
    标题:Role of tyrosine phosphorylation of a cellular protein in adeno-associated virus 2-mediated transgene expression
    发明人:SRIVASTAVA ARUN; QING KEYUN; WANG XU-SHAN; PONNAZHAGAN SELVARANGAN; BAJPAI ANIL
    权利人:ADVANCED RES & TECH INST
    摘要:The present invention identifies a protein, designated the D-sequence-binding protein (D-BP), is phosphorylated at tyrosine residues and blocks AAV-mediated transgene expression in infected cells by inhibiting the leading strand viral DNA synthesis. More particularly, the present invention demonstrates that D-BP is phosphorylated by EGF-R protein tyrosine kinase. Methods of increasing transcription and promoting replication of transgenes exploiting this information are disclosed herein.

    供应商参考报价(招募中)

    品牌试剂参考报价(招募中)

    📌 第三方产品分析报告

    ✅ COA系统入驻 | 共享模式

    主要参考文献


    1: Han Y, Caday CG, Nanda A, Cavenee WK, Huang HJ. Tyrphostin AG 1478 preferentially inhibits human glioma cells expressing truncated rather than wild-type epidermal growth factor receptors. Cancer Res. 1996 Sep 1;56(17):3859-61.
    164:128-32. doi: 10.1016/j.saa.2016.04.009. Epub 2016 Apr 12. 282(6):C1461-8. doi: 10.1152/ajpcell.00398.2001. 90(8):1145-9. doi: 10.1139/y2012-023. Epub 2012 May 30.
    5: Stekelenburg J, Klein BY, Ben-Bassat H, Rojansky N. Opposing effects of cyclosporin A and tyrphostin AG-1478 indicate a role for Src protein in the cellular control of mineralization. J Cell Biochem. 1998 Oct 1;71(1):116-26. doi: 10.1002/(sici)1097-4644(19981001)71:1<116::aid-jcb12>3.0.co;2-l. 342(2):292-9. doi: 10.1016/j.ab.2005.04.002. 131(4):1149-56. doi: 10.1378/chest.06-2031. 410(2-3):187-90. doi: 10.1016/s0014-5793(97)00580-2. 65(3):420-9. 166(1):87-94. doi: 10.1016/j.jss.2009.09.058. Epub 2009 Nov 11. 21(22):8434. doi: 10.3390/ijms21228434.

    合成参考文献


    参考文献:10.1016/j.tox.2011.06.016
    摘要:Carbonari D, Campopiano A, Ramires D, Strafella E, Staffolani S, Tomasetti M, Curini R, Valentino M, Santarelli L, Amati M. Angiogenic effect induced by mineral fibres. Toxicology. 2011 Oct 09;288(1-3):34–42. doi: 10.1016/j.tox.2011.06.016.
    📝 需求与反馈
    尽可能描述清楚需求与问题信息
    ×

    通知