合成目标产物 2,2-Dimethyl-1,3-Dioxane-4,6-Dione 主要起始原料 Malonic Acid And Acetone
(文献来源)合成步骤主要原料 Malonic Acid 和 Acetone
6,6-二甲基-5,7-二氧杂-1,2-二氮杂螺[2.5]辛-1-烯-4,8-二酮置于二苯甲酮体系中,用 甲醇 用作溶剂,以93%的收率获得丙二酸环(亚)异丙酯 参考文献:重氮羰基化合物的化学:Xxvii.1,3-二恶烷-4,6-二酮衍生物二嗪类的热解和光解 标题:重氮羰基化合物的化学:Xxvii.1,3-二恶烷-4,6-二酮衍生物二嗪类的热解和光解 摘要:Photolysis Of Diazirines,1,3-Dioxane-4,6-Dione Derivatives,occurs In The Presence Of Methanol Or Dimethyl Sulfide As Carbene Traps Without A Formation Of Carbene Intermediates. It Was Established For The First Time That The Thermolysis And Photolysis Of Diazirines From The 1,3-Dioxane-4,6-Dione Series Led Mainly To Wolff Rearrangement With A Subsequent Formation Of 5-Oxo-1,3-Dioxolane-4-Carboxylic Acids Or Their Derivatives. The Data Obtained Show That The Alpha-Oxodiazirines Are The Key Intermediates In The Photolysis And Wolff Rearrangement Of Alpha-Diazocarbonyl Compounds. Doi:10.1134/s1070428006080197
专利号:US-2007259917-A1 优先权日:2006-04-24 标题 :Processes for the synthesis of 3-isobutylglutaric acid 发明人:KANSAL VINOD K; CHAURASIA BRIJNATH P; PATEL HITESH K; SHELKE SHIVAJI H; MORE YOGESH P 权利人:KANSAL VINOD K; CHAURASIA BRIJNATH P; PATEL HITESH K; SHELKE SHIVAJI H; MORE YOGESH P 摘要:Provided are processes for the synthesis of 3-isobutylglutaric acid, an intermediate in the synthesis of (S)-Pregabalin.
专利号:US-4287123-A 优先权日:1980-01-14 标题 :Synthesis of thienamycin via (3SR, 4RS)-3-((RS)-1-acyloxyethyl)-2-oxo-4-azetidineacetate 发明人:LIU THOMAS M H; MELILLO DAVID G; RYAN KENNETH M; SHINKAI ICHIRO; SLETZINGER MEYER 权利人:MERCK & CO INC 摘要:Disclosed is a process for the stereocontrolled total synthesis of thienamycin, which synthesis proceeds via intermediate II: II wherein R is a readily removable carboxyl protecting group; and is a readily removable acyl group.
专利号:US-10392361-B2 优先权日:2016-01-21 标题:Process for the synthesis of intermediates of Nebivolol 发明人:BARTOLI SANDRA; MANNUCCI SERENA; GRISELLI ALESSIO; STEFANINI ALESSIO 权利人:MENARINI INT OPERATIONS LUXEMBOURG SA 摘要:The present invention relates to a novel process for the synthesis of the intermediate compounds constituted by chromanyl haloketones of formula III and 6-fluoro-2-(oxiran-2-yl)chromans of formula I. n The intermediates thus obtained can be used for the synthesis of Nebivolol.
专利号:US-11840544-B2 优先权日:2018-07-02 标 题 :Intermediates in the synthesis of C3-substituted cephalosporins 发明人:MADELA KAROLINA 权利人:NORBROOK LAB LTD 摘要:Disclosed herein are novel and inventive methods for preparing intermediates in the synthesis of C3-substituted cephalosporins. One preferred C3-substituted cephalosporin of clinical interest is Cefovecin. Accordingly, the present invention provides for methods of preparing reactive halogen intermediates for use in the synthesis of C3-substituted cephalosporins, such as Cefovecin. In the case of Cefovecin the reactive intermediates are of the formula:
专利号:US-4269772-A 优先权日:1980-01-14 标 题 :Synthesis of thienamycin via trans-3-carboxymethylene-4-carboxy-5-methyl-Δ2 -isoxazoline 发明人:MELILLO DAVID G; RYAN KENNETH M 权利人:MERCK & CO INC 摘要:Disclosed is a process for the stereocontrolled total synthesis of thienamycin, which synthesis proceeds via intermediate II: II wherein R5 and R6 are removable protecting groups.
专利号:US-11459549-B2 优先权日:2018-05-10 标 题:Method for biocatalytic synthesis of Sitagliptin and intermediate thereof 发明人:WU FAHAO; YANG WEN; LI GANG; SHI HONGWEI; GAO YANGZHE; LIU LILI; YUAN ZHIFA 权利人:CHINA FORTUNE WAY COMPANY; NANJING REDWOOD FINE CHEMICAL CO LTD 摘要:Provided is a method for biocatalytic synthesis of Sitagliptin and intermediates thereof, in particular, provided are compounds of Formula (I) and Formula (II), or pharmaceutically acceptable salts thereof, a polypeptide capable of catalyzing conversion of a compound of Formula (I) to a compound of Formula (II), a nucleic acid encoding the polypeptide, a vector and a cell comprising the nucleic acid. In addition, also provided are a method for producing a compound of Formula (II) and Sitagliptin by using the polypeptide and the compound of Formula (I), and a method for preparing the polypeptide.
[参考文献]: Ahmad Shaabani, Et Al. A Novel One-Pot Three-(In Situ Five-)Component Condensation Reaction: An Unexpected Approach For The Synthesis Of Tetrahydro-2,4-Dioxo-1H-Benzo[参考文献]: Bo Jiang, Et Al. A New Domino Autocatalytic Reaction Leading To Polyfunctionalized Spiro[参考文献]: Davood Nematollahi, Et Al. Electrochemical Oxidation Of Catechols In The Presence Of Phenyl-Meldrum'S Acid. Synthesis And Kinetic Evaluation. Chem Pharm Bull (Tokyo). 2010 Jan;58(1):23-6. [参考文献]: Dipak Samanta, Et Al. Self-Assembled Pd6 Open Cage With Triimidazole Walls And The Use Of Its Confined Nanospace For Catalytic Knoevenagel- And Diels-Alder Reactions In Aqueous Medium. Chemistry. 2012 Sep 24;18(39):12322-9. [参考文献]: Harmeet S Sandhu, Et Al. Synthesis And Biological Evaluation Of Arylidene Analogues Of Meldrum'S Acid As A New Class Of Antimalarial And Antioxidant Agents. Bioorg Med Chem. 2010 Aug 1;18(15):5626-33.
合成参考文献
参考文献:10.1107/s1600536811014358 摘要:He YX, Wu JW, Tong RS, Shi JY. 2,2-Dimethyl-5-[(2-nitro-anilino)methyl-idene]-1,3-dioxane-4,6-dione. Acta Crystallogr Sect E Struct Rep Online. 2011 May 01;67(Pt 5):o1216. 参考文献:10.1107/s1600536811016497 摘要:Zeng WL. 5-(3,4-Dimethyl-benzyl-idene)-2,2-dimethyl-1,3-dioxane-4,6-dione. Acta Crystallogr Sect E Struct Rep Online. 2011 Jun 01;67(Pt 6):o1351.