专利号:WO-2009152051-A1 优先权日:2008-06-12 标题:Synthesis of a macrocyclic hcv protease inhibitor 发明人:WANG PENG 权利人:PHENOMIX CORP; WANG PENG 摘要:The present invention provides a method of synthesis of a macrocyclic compound known as a potent inhibitor of a protease produced by the hepatitis C virus (HCV). Inhibition of the viral protease blocks assembly of mature viral particles in an infected mammalian host. The method of synthesis involves a ring-closing metathesis step using a ruthenium catalyst. Hydrogenation and boronate deprotection provide the HCV protease-inhibitory product.
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:US-8163430-B2 优先权日:2000-01-18 标 题:Synthesis of metal compounds under carbothermal conditions 发明人:BARKER JEREMY; SAIDI YAZID; DONG MING; SWOYER JEFFREY 权利人:BARKER JEREMY; SAIDI YAZID; DONG MING; SWOYER JEFFREY; VALENCE TECHNOLOGY INC 摘要:Active materials of the invention contain at least one alkali metal and at least one other metal capable of being oxidized to a higher oxidation state. Preferred other metals are accordingly selected from the group consisting of transition metals (defined as Groups 4-11 of the periodic table), as well as certain other non-transition metals such as tin, bismuth, and lead. The active materials may be synthesized in single step reactions or in multi-step reactions. In at least one of the steps of the synthesis reaction, reducing carbon is used as a starting material. In one aspect, the reducing carbon is provided by elemental carbon, preferably in particulate form such as graphites, amorphous carbon, carbon blacks and the like. In another aspect, reducing carbon may also be provided by an organic precursor material, or by a mixture of elemental carbon and organic precursor material.
专利号:US-4894385-A 优先权日:1985-01-16 标 题:Imidazole derivatives as inhibitors of TXA2 synthesis 发明人:KAWAMOTO ISAO; ENDO ROKURO; MATSUDA KEIICHI; USHIYAMA SHIGERU; OSHIMA TAKESHI 权利人:SANKYO CO 摘要:Compounds of formula (I): ##STR1## (wherein n is 0, 1 or 2 and R 1 , R 2 , R 4 , R 5 , R 6 , X, Y and Z are a variety of groups and atoms) have the ability to inhibit the synthesis of thromboxane A 2 and hence are useful in the treatment or prophylaxis of thrombotic conditions.
专利号:US-2014199585-A1 优先权日:2013-01-17 标 题 :Low Symmetry Molecules And Phosphonium Salts, Methods Of Making And Devices Formed There From 发明人:RUPERT BENJAMIN L; BEER LEANNE 权利人:ESIONIC ES INC 摘要:Synthesis of molecules and salts is disclosed having low average symmetry and their use in many applications, including but not limited to: as electrolytes in electronic devices such as memory devices including static, permanent and dynamic random access memory, as electrolytes in energy storage devices such as batteries, electrochemical double layer capacitors (EDLCs) or supercapacitors or ultracapacitors, electrolytic capacitors, as electrolytes in dye-sensitized solar cells (DSSCs), as electrolytes in fuel cells, as a heat transfer medium, high temperature reaction and/or extraction media, among other applications. In particular, synthesis methods and processes to form molecules and salts having low average symmetry using mixed Grignard reagents are disclosed.
专利号:US-2023391818-A1 优先权日:2020-11-05 标 题:Peptide synthesis method for suppressing defect caused by diketopiperazine formation 发明人:NOMURA KENICHI; KAGE MIRAI; TAMIYA MINORU; KANAZAWA JUNICHIRO 权利人:CHUGAI PHARMACEUTICAL CO LTD 摘要:Solid-phase synthesis of a peptide has a problem that a desired elongation reaction is prevented from proceeding by diketopiperazine and a 6-membered diamine skeleton compound formed when a protective group at the N-terminal is removed. The present inventors have found that when in production of a peptide by a solid-phase method, a peptide in which an amino group at the N-terminal is protected with a protective group having an Fmoc skeleton is treated in a specific solvent with a base having a pKa of 23 or more in acetonitrile as a conjugate acid, and a peptide chain is then elongated, it is possible to solve the problem described above.
参考标题:Mechanism Of Formation Of Organic Carbonates From Aliphatic Alcohols And Carbon Dioxide Under Mild Conditions Promoted By Carbodiimides. Dft Calculation And Experimental Study 作者:Michele Aresta,Angela Dibenedetto,Elisabetta Fracchiolla,Potenzo Giannoccaro,Carlo Pastore,Imre Pápai,Gábor Schubert |发布日期:2005.8.1 摘要:Into A Carbamate And A Secondary Amine, While In The Presence Of Co2, The Dialkyl Carbonate, (Ro)2Co, Is Formed Together With Urea [cyhn−co−nhcy]. The Reaction Has Been Tested With Various Aliphatic Alcohols Such As Methanol, Ethanol, And Allyl Alcohol. It Results In Being A Convenient Route To The Synthesis Of Diallyl Carbonate, In Particular. O-Methyl-N,N'-Dicyclohexyl Isourea Also Reacts With Phenol
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