📜2-Diazo-3-Hydroxypropanoic Acid Ethyl Ester置于rhodium(II) Acetate Dimer体系中,用 二氯甲烷 用作溶剂,化学反应生成3-氧代丙酸乙酯 参考文献:Catalyzed Insertion Reactions Of Substituted α-Diazoesters. A New Synthesis Of Cis-Enoates 标题:Catalyzed Insertion Reactions Of Substituted α-Diazoesters. A New Synthesis Of Cis-Enoates 摘要: Doi:10.1016/s0040-4039(01)82093-1
专利号:WO-2012100419-A1 优先权日:2011-01-26 标 题 :Process for synthesis of 3-(n,n-disubstituted-amino)-2- substituted acrylate 发明人:GU HAINING; LI XIAOLING; ZHANG PENGFEI; ZHANG XIKUN; CHEN LIANG 权利人:HANGZHOU GREAT FOREST BIOMEDICAL LTD; GU HAINING; LI XIAOLING; ZHANG PENGFEI; ZHANG XIKUN; CHEN LIANG 摘要:Disclosed is a process for synthesis of 3-(N,N-disubstituted-amino)-2-substituted acrylate, which comprises carrying out amine-substitution reaction and elimination reaction for 2-substituted formylacetate alkali metal salt represented by formula (III) and amine complex represented by formula (II) in organic solvent 1 to obtain 3-(N,N-disubstituted-amino)-2-substituted acrylate represented by formula (I). The process uses N,N-disubstituted amine and carbon dioxide, or a liquid complex obtained by N,N-disubstituted amine and carbon dioxide as raw material, thereby it doesn't produce a side product influencing environment. The process has the advantages of reacting simply and operating easily.
专利号:US-8742118-B2 优先权日:2011-10-27 标题 :Methods for preparing intermediates of perampanel 发明人:FONTANA FRANCESCO; STABILE PAOLO 权利人:F I S —FABBRICA ITALIANA SINT S P A 摘要:Methods for the synthesis of 2-alkoxy-5-(pyridin-2-yl)pyridine of formula I n nor salts thereof are provided.
专利号:US-4171439-A 优先权日:1975-04-11 标 题 :Antibacterial analogs of isocephalosporins 发明人:CONWAY TERRY T; LIM GARY M F; MENARD MARCEL 权利人:BRISTOL MYERS CO 摘要:There is described the stereoselective total synthesis of novel DELTA 2,3-1,4-morpholine-2-carboxylic acids possessing a fused beta -lactam ring in the 1,6-position and carrying a substituent cis to carbon 5 in the 7-position of the fused ring system represented by the general formula I wherein Z is halo or hydroxyl and X is acylamino. Also included in the invention are compounds of the above formula in which the carboxyl group at the 2-position is protected as by an easily cleavable ester group and salts of both the free acids and carboxyl-protected compounds. The compounds are potent antibacterial agents.
专利号:US-5852180-A 优先权日:1997-11-17 标题:Chemical synthesis of 6-O-alkyl erythromycin A 发明人:PATEL HEMANTKUMAR H 权利人:ABBOTT LAB 摘要:A process of preparing 6-O-alkyl erythromycin A is provided. The process includes the steps of protecting the oxime hydroxyl of 9-oxime erythromycin A with a benzoyl protecting group, protecting the 2'-hydroxyl group and optionally the 4'-hydroxyl group with an O-protecting group, alkylating the 6-hydroxyl, removing the benzoyl and O-protecting groups and deoximating the 9-oxime.
专利号:US-7384964-B2 优先权日:2002-08-23 标题:Synthesis of epothilones, intermediates thereto, analogues and uses thereof 发明人:DANISHEFSKY SAMUEL J; RIVKIN ALEXEY; YOSHIMURA FUMIHIKO; CHOU TING-CHAO; GABARDA ANA E; DONG HUAJIN; WU KAIDA; MOORE MALCOLM A S; DORN DAVID 权利人:SLOAN KETTERING INST CANCER 摘要:The present invention provides compounds of formula (I): n nas described generally and in classes and subclasses herein. The present invention additionally provides pharmaceutical compositions comprising compounds of formula (I) and provides methods of treating cancer comprising administering a compound of formula (I).
专利号:US-9527855-B2 优先权日:2011-06-29 标题:Process for preparing chiral dipeptidyl peptidase-IV inhibitors 发明人:ZACUTO MICHAEL J; DUNN ROBERT F; MOMENT AARON J; JANEY JACOB M; LIEBERMAN DAVID; SHEEN FAYE; BREMEYER NADINE; SCOTT JEREMY; KUETHE JEFFREY T; TAN LUSHI; CHEN QINGHAO 权利人:MERCK SHARP & DOHME; MERCK SHARP & DOHME 摘要:A process for the preparation of pyrazolopyrolidines of structural formula I: n nand W isn n nor P, wherein in P is an amine protecting group. These compounds are useful in the synthesis of dipeptidyl peptidase-IV inhibitors for the treatment of Type 2 diabetes. Also provided are useful intermediates obtained from the process.