CAS: 66946-81-4; 3-Fluoro-1H-Indole

该化合物是用于制药和农用化学研究中广泛使用的一种杂交芳香化合物Indole的氟化衍生物.在3级引入氟原子会增强其反应性和潜力,作为生物活性分子的构件.该化合物在药用化学中特别宝贵,因为氟化常常能提高代谢稳定性,亲性性和结合性.其结构特征使它成为合成非单质药物或离心类的氟化类似物的多功能中间体.3-氟-1H-蛋白的纯性和一致性对于合成应用中可复制的结果至关重要.建议适当处理和储存,因为其对光和湿度敏感.

结构式图片

上下游产品

3,3-difluoro-1,3-dihydro-2H-indol-2-one indole-2,3-dione 1H-indole-3-carboxylic acid

合成工艺路线路线简述

    📜3-吲哚甲酸置于lithium Acetate,Selectfluor体系中,用 水,乙酸乙酯 作为反应溶剂,化学反应 15.0H,以14%的收率获得产物3-氟吲哚
    参考文献:Selectfluor对富含电子的杂芳族羧酸进行脱羧氟化
    标题:Selectfluor对富含电子的杂芳族羧酸进行脱羧氟化
    摘要:富电子的五元杂芳族化合物(包括呋喃,吡唑,异恶唑,噻吩,吲哚,苯并呋喃和吲唑羧酸)与selectfluor的无过渡金属脱羧氟化反应得到了报道.观测到氟化二聚体产物中含氮杂芳族羧酸,例如吲哚和吡唑.已经开发出有效的方法,以在低温下以li 2 Co 3为碱合成2-和3-氟吲哚的单体.
    DOI:10.1021/acs.Orglett.7B00335

    海关参考信息

    专利信息


    专利号:US-2023010886-A1
    优先权日:2019-09-23
    标 题 :Shp2 inhibitors and uses thereof
    发明人:XIE YINONG; BABISS LEE E
    权利人:SUZHOU PUHE BIOPHARMA CO LTD
    摘要:Compounds of Formula 1 as inhibitors of protein tyrosine phosphatase SHP2 are disclosed. The pharmaceutical compositions comprising compounds of Formula 1, methods of synthesis of these compounds, methods of treatment for diseases associated with the aberrant activity of SHP2 such as cancer using these compounds or compositions containing these compounds are also disclosed.

    专利号:US-10561655-B2
    优先权日:2018-03-21
    标 题 :SHP2 inhibitors and uses thereof
    发明人:XIE YINONG; BABISS LEE E
    权利人:SYNBLIA THERAPEUTICS INC
    摘要:Compounds of Formula 1 as inhibitors of protein tyrosine phosphatase SHP2 are disclosed. The pharmaceutical compositions comprising compounds of Formula 1, methods of synthesis of these compounds, methods of treatment for diseases associated with the aberrant activity of SHP2 such as cancer using these compounds or compositions containing these compounds are also disclosed.

    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

    合成参考文献


    摘要:Semeniuk, T.; Hamel, J.-D., Science of Synthesis: Modern Strategies in Organofluorine Chemistry, (2025) 2.
    📝 需求与反馈
    尽可能描述清楚需求与问题信息
    ×

    通知