专利号:US-2011245503-A1 优先权日:2008-11-28 标题 :Enantioselective synthesis of asymmetric beta-carboline intermediates 发明人:SANTOS LEONARDO; ESPINOZA MORAGA MARLENE; SHANKARAJAH NAGULA 权利人:UNIV TALCA 摘要:Described herein is a new asymmetric synthesis of imines to obtain β-carboline derivatives useful as key intermediate compounds for the synthesis of phosphodiesterase inhibitors using a new process with palladium or ruthenium hydride and/or nickel boride to reduce chiral intermediates. The use of chloroformate chiral auxiliaries is further described for the reduction and asymmetric hydrogenation of imines to obtain β-carboline derivatives and intermediate compounds used in the preparation thereof.
专利号:US-5059709-A 优先权日:1990-11-13 标题 :Process for the synthesis of α-[(dialkylamino)substituted-methylene]-β-oxo-(substituted)propanentriles 发明人:DUSZA JOHN P; CHURCH ROBERT F 权利人:AMERICAN CYANAMID CO 摘要:A novel process for producing α-[(dialkylamino) substituted-methylene]β-oxo-(substituted) propanenitriles of the formula: ##STR1## where R, R 1 and R 2 are defined in the specification by reacting a substituted isoxazole with a diaklylamide dimethylacetal is provided.
专利号:US-7910775-B2 优先权日:2003-04-18 标题 :Synthesis of 2-Hydroxy-N,N-dimethyl-3-[[2-[[1(R)-(5-methyl-2-furanyl)propyl]amino]-3,4-dioxo-1-cyclobuten-1-yl]amino]benzamide 发明人:YIN JIANGUO; FU XIAOYONG; ZHANG SHUYI; MCALLISTER TIMOTHY L; KIM-MEADE AGNES S; WINTERS JASON L; SUDHAKAR ANANTHA; SCHUMACHER DORIS P 权利人:SCHERING CORP 摘要:Disclosed is a process for making the compound of formula I: n nusing the compounds of formulas II, Q, and XI or XII:n n nwherein A is selected from the group consisting of Br, Cl and I (with Br being preferred); and R represents (C 1 -C 10 )alkyl. Also disclosed are intermediate compounds that are made in the disclosed process.
专利号:US-2006205961-A1 优先权日:2003-04-18 标 题:Synthesis of 2-hydroxy-N,N-dimethyl-3-[[2-(1(R)-(5-methyl-2-furany)propyl]amino]-3,4-dioxo-1-cyclobuten-1-yl]amino]benzamide
专利号:US-2009048458-A1 优先权日:2003-04-18 标题:Synthesis of 2-hydroxy-n,n-dimethyl-3-[[2-[[1(r)-(5-methyl-2-furanyl)propyl]amino]-3,4-dioxo-1-cyclobuten-1-yl]amino]benzamide
专利号:US-9868712-B2 优先权日:2013-08-30 标 题 :Synthesis of alkylfurans 发明人:MASCAL MARK; DUTTA SAIKAT 权利人:UNIV CALIFORNIA 摘要:The invention provides a method for preparing a 2,5-dialkyl furan. The method includes forming a reaction mixture containing a catalyst, a hydrogen source, and 2-haloalkylfuran starting material under conditions sufficient to form the 2,5-dialkyl furan. The 2-haloalkylfuran starting material can be derived from biomass, and the 2,5-dialkyl furan product can be used as a biofuel or as a chemical feedstock.
[参考文献]: Fu-Chi Chen, Et Al. Antitubercular Constituents From The Stem Wood Of Cinnamomum Kotoense. J Nat Prod. 2005 Sep;68(9):1318-23. [参考文献]: J Jodynis-Liebert, Et Al. Metabolism Of 5-Methyl-2-Furaldehyde In Rat. Iii. Identification And Determination Of 5-Methyl-2-Furylmethylketone. Xenobiotica. 1988 Aug;18(8):887-92. [参考文献]: P S Sujatha, Et Al. Monitoring Cytotoxic Potentials Of Furfuryl Alcohol And 2-Furyl Methyl Ketone In Mice. Food Chem Toxicol. 2008 Jan;46(1):286-92.
合成参考文献
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