专利号:US-7314843-B2 优先权日:2004-01-29 标 题:Method for synthesis of lamellar solids from an amino-alcohol-type organic structuring agent 发明人:BAREA EVA; FORNES VICENTE; CORMA AVELINO; BOURGES PATRICK; GUILLON EMMANUELLE 权利人:INST FRANCAIS DU PETROLE 摘要:The invention relates to a process for synthesis of lamellar solids based on silicates comprising:n i) a mixing stage, during which a mixture that comprises an alkaline metal, a silica source, water and an organic structuring agent is prepared, and ii) a crystallization stage during which this mixture is kept under conditions allowing the formation of a crystalline solid. nn The organic structuring agent that is used in this process comprises an alcohol group and an amine group that are separated by a hydrocarbon chain.
专利号:WO-2012020271-A1 优先权日:2010-08-11 标题 :Process for the preparation of montelukast sodium 发明人:BODI JOZSEF; FARAGO JANOS; SZOEKE KATALIN; UJVARI VIKTOR; TEMESVARI KRISZTINA; ARANYI ANTAL; SANTA ZSUZSANNA; NAGY MELINDA MAGDOLNA 权利人:RICHTER GEDEON NYRT; BODI JOZSEF; FARAGO JANOS; SZOEKE KATALIN; UJVARI VIKTOR; TEMESVARI KRISZTINA; ARANYI ANTAL; SANTA ZSUZSANNA; NAGY MELINDA MAGDOLNA 摘要:The present invention relates to a process for the synthesis of Montelukast sodium of formula I the chemical name of which is [(R)-(E)]-1-[[[1-[3-[2-(7-chloro-2- quinolinyl)ethenyl]phenyl] -3 - [2-( 1 -hydroxy- 1 -methylethyl)phenyl]propyl] thio]methyl] - -cyclopropaneacetic acid sodium salt. The present invention further provides compounds of general formulae V, VI, VIb and VIII as new intermediates.
专利号:US-5174980-A 优先权日:1991-10-04 标题 :Synthesis of crystalline ZSM-35 发明人:HELLRING STUART D; STRIEBEL RANDY F 权利人:MOBIL OIL CORP 摘要:This invention relates to a new form of crystalline material identified as having the structure of ZSM-35, to a new and useful method for synthesizing said crystalline material and to use of said crystalline material prepared in accordance herewith as a catalyst for organic compound, e.g. hydrocarbon compound, conversion.
专利号:US-7115737-B2 优先权日:2003-05-05 标题:Solid phase synthesis of novel biaryl triazine library by suzuki cross coupling 发明人:CHANG YOUNG-TAE 权利人:UNIV NEW YORK 摘要:Two methods are used to produce diaryl trisubstituted triazines. In the first method, cyanuric chloride is first reacted with a 4-alkoxybenzylamine. The product of this reaction is then reacted with a resin-bound amine, such as 4-alkoxybenzylamine, to ensure that the final compound will be bound to a resin. The product of this reaction is then reacted with boronic acid to produce a trisubstituted diaryl triazine. In the second method, cyanuric chloride is reacted with a benzenealkanethiol. The product of this reaction is then reacted with a resin-bound amine, such as 4-alkoxybenzylamine, to ensure that the final compound will be bound to a resin. The product of this reaction is then reacted with m-CPBA to form a sulfone, which is then reacted with a 4-alkoxybenzylamine to form the desired trisubstituted biaryltriazine.
专利号:US-2005192265-A1 优先权日:2003-03-20 标 题:Cycloalkyl, lactam, lactone and related compounds, pharmaceutical compositions comprising same, and methods for inhibiting beta-amyloid peptide release and/or its synthesis by use of such compounds 发明人:THOMPSON RICHARD C; WILKIE STEPHEN; STACK DOUGLAS R; VANMETER ELDON E; SHI QING; BRITTON THOMAS C; AUDIA JAMES E; REEL JON K; MABRY THOMAS E; DRESSMAN BRUCE A; CWI CYNTHIA L; HENRY STEVEN S; MCDANIEL STACEY L; STUCKY RUSSELL D; PORTER WARREN J 摘要:Disclosed are compounds which inhibit β-amyloid peptide release and/or its synthesis, and, accordingly, have utility in treating Alzheimer's disease. Also disclosed are pharmaceutical compositions that include a compound which inhibits β-amyloid peptide release and/or its synthesis as well as methods for treating Alzheimer's disease both prophylactically and therapeutically with such pharmaceutical compositions.