3863-11-4 = 847685-01-2 反应条件:1.1 Reagents: Iodine Chloride Solvents: Acetic Acid; 0.5 H,Rt 标题:Highly Convergent Synthesis Of A Rebeccamycin Analog With Benzothioeno(2,3-A)Pyrrolo(3,4-C)Carbazole As The Aglycone 作者:Wang,Jianji; Soundarajan,Nachimuthu; Liu,Nian; Zimmermann,Kurt; Naidu,B. Narasimhulu 参考文献:Tetrahedron Letters 日期:2005 卷标:46(6) 页码:907-910]
3863-11-4 = 847685-01-2 反应条件:1.1 Reagents: Imidazole,Potassium Tert-Butoxide Solvents: Water; 1 Min,Rt; 30 Min,20 °C 标题:Structure-Based Optimization Of Orally Active & Reversible Metap-2 Inhibitors Maintaining A Tight 'Molecular Budget' 作者:Hirst,David J.; Brandt,Martin; Bruton,Gordon; Christodoulou,Erica; Cutler,Leanne; Et Al 参考文献:Bioorganic & Medicinal Chemistry Letters 日期:2020 卷标:30(21)]
3863-11-4 = 847685-01-2 反应条件:1.1 Reagents: Sodium Bicarbonate,Iodine Solvents: Water; 3 H,70 °C 标题:Synthesis Of Polyfluorinated Ortho-Alkynylanilines 作者:Politanskaya,Larisa V.; Chuikov,Igor P.; Kolodina,Ekaterina A.; Shvartsberg,Mark S.; Shteingarts,Vitalij D. 参考文献:Journal Of Fluorine Chemistry 日期:2012 卷标:135 页码:97-107]
3863-11-4 = 847685-01-2 反应条件:1.1 Reagents: Acetic Acid,N-Iodosuccinimide; 1 H,Rt 标题:New Indolo[1,2-C]Quinazolines For Single-Crystal Field-Effect Transistor: A United Experimental And Theoretical Studies 作者:Puli,Venkat Swamy; Kilaru,Suresh; Bhongiri,Yadagiri; Marri,Sreenath Reddy; Tripathi,Anuj; Et Al 参考文献:Journal Of Physical Organic Chemistry 日期:2021 卷标:34(12)]
3863-11-4 = 847685-01-2 [标题:Reaction Conditions 标题:Palladium-Catalyzed Chloroimination Of Imidoyl Chlorides To A Triple Bond: An Intramolecular Reaction Leading To 4-Chloroquinolines 作者:Isobe,Akira; Takagi,Jun; Katagiri,Toshimasa; Uneyama,Kenji 参考文献:Organic Letters 日期:2008 卷标:10(13) 页码:2657-2659
专利号:US-12152038-B2 优先权日:2017-09-05 标 题:Vasopressin receptor antagonists and products and methods related thereto 发明人:JONES ROBERT M; URBANO MARIANGELA; BRANDT GARY; CHAMBERS MARK; HARDICK DAVID; KNIGHT CHRIS; TIERNEY JASON; LOCK CHRIS 权利人:NEUMORA THERAPEUTICS INC 摘要:Compounds are provided that antagonize vasopressin receptors, particularly the V1a receptor products containing such compounds, as well as to methods of their use and synthesis. Such compounds have the structure of Formula (I), or a pharmaceutically acceptable isomer, racemate, hydrate, solvate, isotope, or salt thereof:wherein Q1, Q2, Q3, R2a, R2b, R3 and X are as defined herein.
专利号:WO-2010001220-A1 优先权日:2008-07-01 标 题 :New 1,2,4-triazine derivatives and biological applications thereof 发明人:DESROY NICOLAS; DENIS ALEXIS; GERUSZ VINCENT; OLIVEIRA CHRYSTELLE; VONGSOUTHI VANIDA; MOREAU FRANCOISE; ESCAICH SONIA 权利人:MUTABILIS SA; DESROY NICOLAS; DENIS ALEXIS; GERUSZ VINCENT; OLIVEIRA CHRYSTELLE; VONGSOUTHI VANIDA; MOREAU FRANCOISE; ESCAICH SONIA 摘要:The invention relates to new 1,2,4-triazine derivatives of formula (I): wherein A, B, R2 and Y are defined in the application, their preparation and intermediates, their use as drugs and pharmaceutical compositions and associations containing them. The compounds of formula (I) are capable of inhibiting bacterial heptose synthesis.
参考文献:10.1055/s-0036-1591504 摘要:Politanskaya L, Tretyakov E. p-Toluenesulfonic Acid Induced Conversion of Fluorinated Trimethylsilylethynylanilines into Aminoacetophenones: Versatile Precursors for the Synthesis of Benzoazaheterocycles. Synthesis. 2017 Oct 25;50(03):555–64. doi: 10.1055/s-0036-1591504.