合成目标产物 (Trifluoromethyl)Trimethylsilane 主要起始原料 Chlorotrimethylsilane And Bromotrifluoromethane
75-77-4 + 426-58-4 = 81290-20-2 反应条件:1.1 Reagents: Magnesium Solvents: Dimethylformamide; 2 Min,0 °C1.2 Solvents: Dimethylformamide; 2 H,0 °C -> Rt 标题:Preparation Of Tri- And Difluoromethylsilanes Via An Unusual Magnesium Metal-Mediated Reductive Tri- And Difluoromethylation Of Chlorosilanes Using Tri- And Difluoromethyl Sulfides,Sulfoxides,And Sulfones 作者:Prakash,G. K. Surya; Et Al 参考文献:Journal Of Organic Chemistry 日期:2003 卷标:68(11) 页码:4457-4463]
75-77-4 + 703-18-4 = 81290-20-2 反应条件:1.1 Reagents: Magnesium Solvents: Dimethylformamide; 2 Min,0 °C1.2 Solvents: Dimethylformamide; 30 Min,0 °C; 1.5 H,Rt 标题:Preparation Of Tri- And Difluoromethylsilanes Via An Unusual Magnesium Metal-Mediated Reductive Tri- And Difluoromethylation Of Chlorosilanes Using Tri- And Difluoromethyl Sulfides,Sulfoxides,And Sulfones 作者:Prakash,G. K. Surya; Et Al 参考文献:Journal Of Organic Chemistry 日期:2003 卷标:68(11) 页码:4457-4463]
75-77-4 + 31270-13-0 = 81290-20-2 反应条件:1.1 Solvents: Tetrahydrofuran; 10 Min,Rt 标题:Borazine-Cf3- Adducts For Rapid,Room Temperature,And Broad Scope Trifluoromethylation 作者:Geri,Jacob B.; Et Al 参考文献:Angewandte Chemie 日期:2018 卷标:57(5) 页码:1381-1385]
2314-97-8 + 75-77-4 = 81290-20-2 [标题:Reaction Conditions 标题:Trifluoroiodomethane - First Update To Document Cited In Ca149:287755 作者:Burton,Donald J.; Et Al 参考文献:E-Eros Encyclopedia Of Reagents For Organic Synthesis 日期:2007]
75-77-4 = 81290-20-2 反应条件:1.1 Reagents: Tetrabutylammonium Bromide Solvents: Dimethylformamide 标题:An Efficient Inexpensive Electrochemical Preparation Of Ruppert'S Reagent 作者:Aymard,Frederic; Et Al 参考文献:Tetrahedron Letters 日期:1994 卷标:35(46) 页码:8623-4]
109111-29-7 = 81290-20-2 反应条件:1.1 Reagents: Methylmagnesium Bromide Solvents: Butyl Ether1.2 Reagents: Hydrochloric Acid Solvents: Water 标题:Synthesis And Properties Of (Trifluoromethyl)Trichlorosilane,A Versatile Precursor For (Trifluoromethyl)Silyl Compounds 作者:Beckers,H.; Et Al 参考文献:Journal Of Organometallic Chemistry 日期:1986 卷标:316(1-2) 页码:41-50]
402-31-3 = 81290-20-2 反应条件:1.1 Reagents: Cyclohexene Solvents: Tetrahydrofuran; 40 Min,45 °C 标题:Mechanism Of The Rhodium-Catalyzed Silylation Of Arene C-H Bonds 作者:Cheng,Chen; Et Al 参考文献:Journal Of The American Chemical Society 日期:2014 卷标:136(34) 页码:12064-12072]
= 81290-20-2 反应条件:1.1 Reagents: Trimethylsilyl Triflate Solvents: Toluene; Rt; 12 H,60 °C 标题:Siladifluoromethylation And Difluoromethylation Onto C(Sp3),C(Sp2),And C(Sp) Centers Using Ruppert-Prakash Reagent And Fluoroform 作者:Aikawa,Kohsuke; Et Al 参考文献:Organic Letters 日期:2016 卷标:18(14) 页码:3354-3357]
75-77-4 = 81290-20-2 反应条件:1.1 Reagents: Potassium Bis(Trimethylsilyl)Amide Solvents: Toluene; 30 Min,-85 °C; 5 H,-85 °C; -85 °C -> 33 °C; 3 H,31 - 33 °C 标题:Nhc Catalysed Trimethylsilylation Of Terminal Alkynes And Indoles With Ruppert'S Reagent Under Solvent Free Conditions 作者:Arde,Panjab; Et Al 参考文献:Rsc Advances 日期:2014 卷标:4(91) 页码:49775-49779]
75-77-4 + 426-58-4 = 81290-20-2 [标题:Reaction Conditions 标题:Ortho Acid Derivatives. Trihalomethyl Compounds 作者:Prakash,G. K. S.; Et Al 参考文献:Science Of Synthesis 日期:2005 卷标:22 页码:617-668]
75-77-4 + 703-18-4 = 81290-20-2 反应条件:1.1 Reagents: Magnesium Solvents: Dimethylformamide 标题:Trifluoromethyltrimethylsilane - First Update To Document Cited In Ca149:287793 作者:Olah,George A.; Et Al 参考文献:E-Eros Encyclopedia Of Reagents For Organic Synthesis 日期:2007]
2314-97-8 + 75-77-4 = 81290-20-2 [标题:Reaction Conditions 标题:Tetrahetero-Substituted Methanes With A Carbon-Halogen Bond 作者:Il'Chenko,A. Y. 参考文献:Science Of Synthesis 日期:2005 卷标:18 页码:1135-1201]
3385-94-2 + 135039-77-9 = 81290-20-2 反应条件:1.1 Catalysts: Tetrabutylammonium Fluoride Solvents: Tetrahydrofuran 标题:Synthetic Methods. 197. Facile Preparation Of (Trifluoromethyl)Tributyltin And Transtrifluoromethylation Of Disilyl Sulfides To The Corresponding Trifluoromethylsilanes 作者:Surya Prakash,G. K.; Et Al 参考文献:Synlett 日期:1996 卷标:(2) 页码:151-3]
75-77-4 = 81290-20-2 反应条件:1.1 Reagents: Potassium Bis(Trimethylsilyl)Amide Solvents: Toluene; -85 °C; 20 Min,-85 °C1.2 98 Min,-85 °C; 5 H,-85 °C; -85 °C -> Rt; 2 H,Rt 标题:Taming Of Fluoroform: Direct Nucleophilic Trifluoromethylation Of Si,B,S,And C Centers 作者:Prakash,G. K. Surya; Et Al 参考文献:Science (Washington 日期:2012 卷标:338(6112) 页码:1324-1327]
75-77-4 + 456-56-4 = 81290-20-2 反应条件:1.1 Reagents: Magnesium Solvents: Dimethylformamide; 2 Min,0 °C1.2 Solvents: Dimethylformamide; 4 H,Rt 标题:Preparation Of Tri- And Difluoromethylsilanes Via An Unusual Magnesium Metal-Mediated Reductive Tri- And Difluoromethylation Of Chlorosilanes Using Tri- And Difluoromethyl Sulfides,Sulfoxides,And Sulfones 作者:Prakash,G. K. Surya; Et Al 参考文献:Journal Of Organic Chemistry 日期:2003 卷标:68(11) 页码:4457-4463]
402-31-3 + 1873-88-7 = 81290-20-2 反应条件:1.1 Reagents: Cyclohexene Catalysts: (Sp-5-23)-[1,1′-[(1R)-6,6′-Dimethoxy[1,1′-Biphenyl]-2,2′-Diyl]Bis[1,1-Bis(3,4,5-...; 50 °C 标题:Mechanism Of The Rhodium-Catalyzed Silylation Of Arene C-H Bonds 作者:Cheng,Chen; Et Al 参考文献:Journal Of The American Chemical Society 日期:2014 卷标:136(34) 页码:12064-12072
专利号:WO-2012047907-A9 优先权日:2010-10-04 标题 :Synthesis of c5-substituted tetracyclines, uses thereof, and intermediates thereto 发明人:MYERS ANDREW G; WRIGHT PETER M; HECKER EVAN 权利人:HARVARD COLLEGE; MYERS ANDREW G; WRIGHT PETER M; HECKER EVAN 摘要:The tetracycline class of antibiotics has played a major role in the treatment of infectious diseases for the past 50 years. However, the increased use of the tetracyclines in human and veterinary medicine has led to resistance among many organisms previously susceptible to tetracycline antibiotics. The recent development of a modular synthesis of tetracycline analogs through a chiral enone intermediate has allowed for the efficient synthesis of novel tetracycline analogs never prepared before. The present invention provides more efficient routes for preparing the enone intermediate and allows for a wide variety of substituents at position 5 of the tetracycline ring system.
专利号:US-2006167025-A1 优先权日:2004-12-22 标 题:Tricyclic amino alcohols, processes for synthesis of same and use of same as anti-inflammatory drugs 发明人:BERGER MARKUS; SCHMEES NORBERT; SCHAECKE HEIKE; BAURLE STEFAN; REHWINKEL HARTMUT; MENGEL ANNE; KROLIKIEWICZ KONRAD; GROSSBACH DANJA; VOIGTLAENDER DAVID 权利人:BERGER MARKUS; SCHMEES NORBERT; SCHAECKE HEIKE; BAURLE STEFAN; REHWINKEL HARTMUT; MENGEL ANNE; KROLIKIEWICZ KONRAD; GROSSBACH DANJA; VOIGTLAENDER DAVID 摘要:The invention relates to tricyclic amino alcohols of general formula (I) n nmethod for synthesis of same and use of same as anti-inflammatory agents.
专利号:US-2015336866-A1 优先权日:2013-01-01 标题:Synthesis of difluoromethyl ethers and sulfides 发明人:HARTWIG JOHN; FIER PATRICK 权利人:UNIV CALIFORNIA 摘要:The synthesis of difluoromethyl ethers and sulfides with a simple, non-ozone-depleting reagent is described. The difluoromethylation of phenols with this reagent occurs at room temperature within minutes with exceptional functional group tolerance. The mild conditions makes possible tandem processes for the conversion of aryl boronic acids, aryl halides and arenes to difluoromethyl ethers. Mechanistic studies support a reaction pathway involving nucleophilic attack of the phenolate to difluorocarbene.
专利号:US-7507843-B2 优先权日:2003-10-16 标题:Stereoselective synthesis of certain trifluoromethyl-substituted alcohols 发明人:SONG JINHUA J; TAN ZHULIN; XU JINGHUA; YEE NATHAN K; SENANAYAKE CHRIS H 权利人:BOEHRINGER INGELHEIM PHARMA 摘要:A process for stereoselective synthesis of compounds of Formula X wherein: R1 is an aryl or heteroaryl group, each optionally independently substituted with one to three substituent groups, wherein each substituent group of R1 is independently C1-C5 alkyl, C2-C5 alkenyl, C2-C5 alkynyl, C3-C8 cycloalkyl, heterocyclyl, aryl, heteroaryl, C1-C5 alkoxy, C2-C5 alkenyloxy, C2-C5 alkynyloxy, aryloxy, C1-C5 alkanoyloxy, C1-C5 alkanoyl, aroyl, trifluoromethyl, trifluoromethoxy, or C1-C5 alkylthio, wherein each substituent group of R1 is optionally independently substituted with one to three substituent groups selected from methyl, methoxy, fluoro, chloro, hydroxy, oxo, cyano, or amino; and R2 and R3 are each independently hydrogen or C1-C5 alkyl, or R2 and R3 together with the carbon atom they are commonly attached to form a C3-C8 spiro cycloalkyl ring.
专利号:US-2025129021-A1 优先权日:2023-09-19 标 题:Small molecule protein synthesis modulators 发明人:GYGI DAVID; BAHMANYAR SOGOLE SAMI; HAMANN LAWRENCE 权利人:INTERDICT BIO INC 摘要:The present disclosure provides compounds of the formulae herein (e.g., Formula (I), Formula (V)), and pharmaceutically acceptable salts thereof, which are useful for modulating protein synthesis (e.g., modulating synthesis of BCL-2, MYC, CCND1, MCL-1, ALK, KRAS-G12D). The present disclosure also provides pharmaceutical compositions and kits comprising the compounds, or pharmaceutically acceptable salts thereof, and methods of treating or preventing diseases or disorders (e.g., diseases or disorders associated with BCL-2, MYC, CCND1, MCL-1, ALK, KRAS-G12D) by administering to a subject in need thereof the compounds, or pharmaceutically acceptable salts thereof, or pharmaceutical compositions thereof.
专利号:US-2025091989-A1 优先权日:2023-09-19 标 题 :Small molecule protein synthesis modulators 发明人:GYGI DAVID; BAHMANYAR SOGOLE SAMI; HAMANN LAWRENCE 权利人:INTERDICT BIO INC 摘要:The present disclosure provides compounds of the formulae herein (e.g., Formula (I)), and pharmaceutically acceptable salts thereof, which are useful for modulating protein synthesis (e.g., modulating synthesis of BCL-2, MYC, CCND1, MCL-1, ALK, KRAS-G12D). The present disclosure also provides pharmaceutical compositions and kits comprising the compounds, or pharmaceutically acceptable salts thereof, and methods of treating or preventing diseases or disorders (e.g., diseases or disorders associated with BCL-2, MYC, CCND1, MCL-1, ALK, KRAS-G12D) by administering to a subject in need thereof the compounds, or pharmaceutically acceptable salts thereof, or pharmaceutical compositions thereof.