专利号:US-2009177008-A1 优先权日:2005-12-28 标题:Novel process for synthesis of itopride and its novel intermediate n-(4-hydroxybenzyl)- 3,4-dimethoxybenzamide 发明人:KHAMAR BAKULESH MAFATLAL; MODI INDRAVADAN AMBALAL; VENKATRAMAN JAYARAMAN; RAVI PONNAIAH; NORI DIVAKARA SOMAYAJULU; GAJULA MADHUSUDANA RAO; RENUGADEVI GURUSAMY; SHASHIKALA KUNJARU N; RUDRAMUNI SANTOSH M 权利人:CADILA PHARMACEUTICALS LTD 摘要:The present invention relates to a novel and improved process for the preparation of N-[4-[2-(dimethylamino)ethoxy]benzyl]-3,4-dimethoxybenzamide—known as Itopride, via a novel intermediate N-(4Ëœhydroxybenzyl)-3,4-dimethoxybenzamide.
专利号:US-2025259704-A1 优先权日:2022-06-24 标 题:Systems and methods for cell-free iterative site saturation mutagenesis and its application for the directed evolution of enzymes catalyzing unnatural reactions 发明人:JEWETT MICAHEL C; BOGART JONATHAN W; LANDWEHR GRANT M; Karim Ashty Stephen 权利人:UNIV NORTHWESTERN 摘要:Disclosed are methods, compositions, systems, and protein compounds for the directed evolution of enzymes and proteins. The method comprising generating variant protein with a desired functionality, comprising one or more DNA expression templates comprising nucleic acid sequences encoding a variant protein, expressing the variant protein using cell-free protein synthesis; and analyzing one or more parameters associated with the variant protein.
专利号:WO-2007074386-A9 优先权日:2005-12-28 标 题 :A novel process for synthesis of itopride and it’s novel intermediate-n-(4-hydroxybenzyl)-3,4-dimethoxybenzamide
专利号:WO-2007074386-A2 优先权日:2005-12-28 标题 :A novel process for synthesis of itopride and it’s novel intermediate-n-(4-hydroxybenzyl)-3,4-dimethoxybenzamide
参考标题:Ex Situ Generation Of Stoichiometric And Substoichiometric 12Co And 13Co And Its Efficient Incorporation In Palladium Catalyzed Aminocarbonylations 作者:Philippe Hermange,Anders T. Lindhardt,Rolf H. Taaning,Klaus Bjerglund,Daniel Lupp,Troels Skrydstrup |发布日期:2011.4.20 摘要:Co-Precursor Led To The Development Of A New Solid, Stable, And Easy To Handle Source Of Co For Chemical Transformations. The Synthesis Of This Co-Precursor Also Provided An Entry Point For The Late Installment Of An Isotopically Carbon-Labeled Acid Chloride For The Subsequent Release Of Gaseous [(13)C]Co. In Combination With Studies Aimed Toward Application Of Co As The Limiting Reagent, This Method Provided