CAS: 887266-99-1; 3-Fluoro-4-Iodobenzonitrile

该化合物是一个氟化和碘化芳烃硝酸盐化合物,在合成有机化学方面有很大作用,其独特的结构包括苯硝酸盐的氟和碘替代物,它使它成为交织反应的多用途中间体,如铃木-米亚乌拉和Sonogashira的联动.电镀硝酸盐组增强了核分裂生物替代反应的再活性,而碘原子则成为进一步功能化的处理器.该复合物在制造复杂分子的制药和农用化学研究中特别有用. 它在标准条件下的高度纯度和稳定性确保了要求合成应用的可靠性能.

结构式图片

欧盟法规

ECHA物质C&L通报

上下游产品

CAS号1150114-77-4 4-氰基-2-氟苯基硼酸

合成工艺路线路线简述

  • 63069-50-1 = 887266-99-1
    反应条件:1.1 Reagents: Sodium Nitrite,Potassium Iodide Catalysts: P-Toluenesulfonic Acid Solvents: Acetonitrile; 2 H,0 °C -> Rt
    标题:Discovery Of 5-(2-Chloro-4'-(1H-Imidazol-1-Yl)-[1,1'-Biphenyl]-4-Yl)-1H-Tetrazole As Potent And Orally Efficacious S-Nitrosoglutathione Reductase (Gsnor) Inhibitors For The Potential Treatment Of Copd
    作者:Muthukaman,Nagarajan; Deshmukh,Sanjay; Tondlekar,Shital; Tambe,Macchindra; Pisal,Dnyandeo; Et Al
    参考文献:Bioorganic & Medicinal Chemistry Letters 日期:2018 卷标:28(23-24) 页码:3766-3773
3-氟-4-氨基苯腈置于对甲苯磺酸,Potassium Iodide,Sodium Nitrite体系中,用 乙腈,水 作为反应溶剂,化学反应 5.0H,以4.0 G的收率获得产物3-氟-4-碘苯腈
参考文献: Alkyne Compounds As S-Nitrosoglutathione Reductase Inhibitors[fr] Composés De Type Alcyne En Tant Qu'Inhibiteurs De La S-Nitrosoglutathione Réductase
标题: Alkyne Compounds As S-Nitrosoglutathione Reductase Inhibitors[fr] Composés De Type Alcyne En Tant Qu'Inhibiteurs De La S-Nitrosoglutathione Réductase
摘要:提供的是式(Ia)的化合物及其药学上可接受的盐,其中a,B,R1,R2,M和n如本文所定义,这些化合物作为s-硝基谷胱甘肽还原酶(Gsnor)的抑制剂具有活性.这些化合物可以预防,抑制或抑制gsnor的作用,因此在治疗gsnor介导的疾病,疾病,综合征或病症方面具有用处,例如肺动脉高压,急性呼吸窘迫综合征(Ards),哮喘,支气管痉挛,咳嗽,肺炎,肺纤维化,间质性肺疾病,囊性纤维化和慢性阻塞性肺疾病(Copd).

海关参考信息

专利信息


专利号:WO-2025128848-A1
优先权日:2023-12-12
标题:Heterocyclic compounds as triggering receptor expressed on myeloid cells 2 agonists and methods of use
发明人:HOUZE JONATHAN B; PANDYA BHAUMIK
权利人:VIGIL NEUROSCIENCE INC
摘要:The present disclosure provides compounds of Formula (I), useful for the activation of Triggering Receptor Expressed on Myeloid Cells 2 ('TREM2'). This disclosure also provides pharmaceutical compositions comprising the compounds, uses of the compounds, and compositions for treatment of, for example, a neurodegenerative disorder. Further, the disclosure provides intermediates useful in the synthesis of compounds of Formula (I).

专利号:US-9868746-B2
优先权日:2012-02-23
标题:Substituted 5-aminothieno[2,3-C]pyridazine-6-carboxamide analogs as positive allosteric modulators of the muscarinic acetylcholine receptor M4
发明人:LINDSLEY CRAIG W; CONN P JEFFREY; WOOD MICHAEL R; MELANCON BRUCE J; TARR JAMES C; SALOVICH JAMES M; POSLUSNEY MICHAEL S
权利人:UNIV VANDERBILT
摘要:In one aspect, the invention relates to substituted 5-aminothieno[2,3-c]pyridazine-6-carboxamide analogs, derivatives thereof, and related compounds, which are useful as positive allosteric modulators of the muscarinic acetylcholine receptor M 4 (mAChR M 4 ); synthesis methods for making the compounds; pharmaceutical compositions comprising the compounds; and methods of treating neurological and psychiatric disorders associated with muscarinic acetylcholine receptor dysfunction using the compounds and compositions. This abstract is intended as a scanning tool for purposes of searching in the particular art and is not intended to be limiting of the present invention.

专利号:US-8344010-B2
优先权日:2008-12-26
标 题 :Fused imidazole derivatives as TRPV3 antagonist
发明人:LINGAM V S PRASADARAO; THOMAS ABRAHAM; PHATANGARE SHANTARAM KASHINATH; MINDHE AJIT SHANKAR; KHATIK JAVED YUSUF; KHAIRATKAR-JOSHI NEELIMA; KATTIGE VIDYA GANAPATI
权利人:GLENMARK PHARMACEUTICALS SA; LINGAM V S PRASADARAO; THOMAS ABRAHAM; PHATANGARE SHANTARAM KASHINATH; MINDHE AJIT SHANKAR; KHATIK JAVED YUSUF; KHAIRATKAR-JOSHI NEELIMA; KATTIGE VIDYA GANAPATI
摘要:The present invention provides transient receptor potential vanilloid (TRPV) modulators of formula (I). In particular, compounds described herein are useful for treating or preventing diseases, conditions and/or disorders modulated by TRPV3. Also provided herein are processes for preparing compounds described herein, intermediates used in their synthesis, pharmaceutical compositions thereof, and methods for treating or preventing diseases, conditions and/or disorders modulated by TRPV3.
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