📜7-溴-2,4-二甲基-喹啉置于lithium体系中,用 四氢呋喃 用作溶剂,化学反应 10.0H,以100%的收率获得2,4-二甲基喹啉 参考文献:Ultrasound-Promoted Coupling Of Aryl And Heteroaryl Halides In The Presence Of Lithium Wire 标题:Ultrasound-Promoted Coupling Of Aryl And Heteroaryl Halides In The Presence Of Lithium Wire 摘要:Although Sonochemical Reactions Of Bromobenzene And Of 2-,3-And 4-Halogenopyridines With Lithium Wire In Thf Solution Yield The Expected Dimers,Considerable Dehalogenation Also occurs,As Monitored By C-13-NMR Spectroscopy. A Pathway For The Unusual Formation Of 4,4'-Bipyridyl From The 2-Halogenopyridines Is Proposed. No Dimers Were Detected From The Reactions With 2-Bromo-4-Methylquinoline And 7-Bromo-2,4-Dimethylquinoline. The Synthetic Potential Of Their Alternative Facile Sonochemical Dehalogenation Is Propounded. Doi:10.1007/bf00809805
专利号:US-11104702-B2 优先权日:2017-07-18 标题 :Process and intermediates for the synthesis of obeticholic acid and derivatives thereof 发明人:HERRÃ?IZ SIERRA IGNACIO; FERNÃ?NDEZ SAINZ YOLANDA; CORDOVILLA LOSADA CARLOS; PÉREZ ENCABO ALFONSO; TURIEL HERNANDEZ JOSÉ ANGEL 权利人:CRYSTAL PHARMA SAU 摘要:A process for the preparation of obeticholic acid and derivatives thereof by:(a) hydrogenation of the double bond and reductive opening of the epoxide of a compound of formula (II) or a salt or solvate thereofto obtain a compound of formula (IIIa) and/or (IIIb), or salts or solvates thereofand(b) conversion of a compound of formula (IIIa) and/or a compound of formula (IIIb), or a salt or solvate thereof, into a compound of formula (I), or a salt or solvate thereof
专利号:US-2007060558-A1 优先权日:2004-07-30 标 题 :Hybrid molecules QA where Q is an aminoquinoline and A is an antibiotic residue, the synthesis and uses thereof as antibacterial agents 发明人:SANCHEZ MURIEL; MEUNIER BERNARD 权利人:CENTRE NAT RECH SCIENT 摘要:The invention concerns an aminoquinoline-antibiotic hybrid compound of general formula (I): Q—(Y 1 ) p —(U) p —(Y 2 ) p -A: wherein Q represents an aminoquinoline, (Y 1 ) p (U) p —(Y 2 ) p″ is an optional spacer and A is an antibiotic residue. The invention enables the antibiotic residue activity to be unexpectedly enhanced.
专利号:EP-3431486-A1 优先权日:2017-07-18 标题 :Process and intermediates for the synthesis of obeticholic acid and derivatives thereof
专利号:WO-2019015914-A1 优先权日:2017-07-18 标 题 :METHODS AND INTERMEDIATES FOR THE SYNTHESIS OF OBETICHOLIC ACID AND DERIVATIVES THEREOF
专利号:US-2020165289-A1 优先权日:2017-07-18 标 题 :Process and intermediates for the synthesis of obeticholic acid and derivatives thereof
专利号:EP-3655419-A1 优先权日:2017-07-18 标题 :Process and intermediates for the synthesis of obeticholic acid and derivatives thereof