环己醇置于三(三甲基硅基)硅烷,三乙胺,1,1'-偶氮(氰基环己烷)体系中,用 四氢呋喃,苯 作为反应溶剂,化学反应 90.0H,反应生成 二苯基环己基膦 参考文献:Radical Phosphination Of Organic Halides And Alkyl Imidazole-1-Carbothioates 标题:Radical Phosphination Of Organic Halides And Alkyl Imidazole-1-Carbothioates 摘要:Taking Advantage Of A Radical-Based Methodology,Mild And Chemoselective Phosphination Reactions Of Organic Halide And Alkyl Imidazole-1-Carbothioates Have Been Developed. The Mild Reaction Conditions Allow Labile Functional Groups To Survive During The Reaction. DOI:10.1021/ja058783H
专利号:US-10889599-B2 优先权日:2018-02-27 标 题:1,1-diborylalkyl-1-metal compounds, preparation method thereof, and their applications toward synthesis of 1,1-diboronate ester compounds 发明人:CHO SEUNG HWAN; LEE YEOSAN 权利人:POSTECH ACAD IND FOUND 摘要:The present invention relates to a 1,1-diborylalkyl-1-metal compound including one metal group together with two identical boron groups at the sp3 carbon center, and its use. Specifically, the present invention relates to development of novel organic reactions, synthesis of functional molecules, and synthesis of new drugs by applying the novel 1,1-diboryl-1-metal substituted alkyl compounds to various molecular libraries which could not be synthesized by conventional methodologies.
专利号:US-2023286918-A1 优先权日:2020-07-02 标 题:Manufacturing process for 3,5-dichloropicolinonitrile for synthesis of vadadustat 发明人:JURKAUSKAS VALDAS; JUNG YOUNG CHUN; KWON TAESOO; KANNAN ARUNACHALAM; GONDI VIJAYA BHASKER 权利人:AKEBIA THERAPEUTICS INC 摘要:Disclosed herein are methods and processes of preparing vadadustat or a pharmaceutically acceptable salts thereof, and intermediates (e.g., a compound of Formula (I), (I-F), (II), or (IV), or a pharmaceutically acceptable salts thereof) useful for the synthesis of vadadustat.
专利号:WO-2021033165-A1 优先权日:2019-08-21 标 题:Process for synthesis of pyrazolidinone compounds 发明人:MATHUR SUCHET SARAN; MHATRE HRIDAYNATH VISHWANATH; PEDHAVI VISHAL PARSHURAM 权利人:GHARDA CHEMICALS LTD 摘要:The present disclosure relates to a process for the synthesis of pyrazolidinone, particularly alkyl 2-(3-chloropyridin-2-yl)-5-oxo-pyrazolidine-3-carboxylate (pyrazolidinone) compound. The process of the present disclosure is simple, economical, and produces alkyl 2-(3-5 chloropyridin-2-yl)-5-oxo-pyrazolidine-3-carboxylate with a comparatively high yields.
专利号:US-12049470-B2 优先权日:2021-02-01 标 题 :MK2 inhibitors, the synthesis thereof, and intermediates thereto 发明人:RUCHELMAN ALEXANDER L; COOMBS JOHN R; ZHU KEMING; LIM DANIEL; JOE CANDICE LEE; GEORGE DAVID T; ZHENG BIN; LIN DONG 权利人:CELGENE CORP 摘要:The present disclosure provides novel synthetic intermediates useful in the synthesis of MK2 kinase inhibitors.
专利号:WO-2025024449-A1 优先权日:2023-07-24 标 题:Processes and intermediates for synthesis of mrtx1133 发明人:GHARBAOUI TAWFIK; SCATTOLIN THOMAS; CHEN CHENG 权利人:MIRATI THERAPEUTICS INC 摘要:The present invention relates to new synthetic routes of synthesizing MRTX1133. The invention also provides intermediates used in the provided synthetic routes.
专利号:US-2022056025-A1 优先权日:2018-09-25 标 题:Synthesis of pyrido[2,3-d]pyrimidin-7(8h)-ones 发明人:BROWN ADAM ROSS; DESROSIERS JEAN-NICOLAS; DUAN SHENGQUAN; HAWKINS JOEL MICHAEL; HAYWARD CHERYL MYERS; MALONEY MARK THOMAS; MONFETTE SEBASTIEN; PERFECT HAHDI HAKIMIOUN; WIDLICKA DANIEL WILLIAM 权利人:PFIZER 摘要:This invention relates to novel methods to prepare substituted pyrido[2,3-d]pyrimidin-7(8H)-ones, and salts and stereoisomers thereof, as well as intermediates useful for the preparation of such compounds.
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