MK-0767, MK-767, KRP-297
Chemical Name: 5-(2,4-Dioxothiazolidin-5-ylmethyl)-2-methoxy-N-[4-(trifluoromethyl)benzyl]benzamide
CAS No. 185808-55-3
项目整合开发状态: Discontinued
项目研究机构: Kyorin (Originator), Merck & Co. (Licensee), Banyu (Codevelopment)
合成路线:1) The Knoevenagel condensation of aldehyde (I) with rhodanine (II) using NH4OAc and AcOH afforded benzylidene- thiazolidine (III).The methyl ester group of (III) was hydrolyzed with HCl in AcOH,and the resulting carboxylic acid (IV) was coupled to 4-(trifluoromethyl)benzylamine (V) in the presence of diethyl phosphorocyanidate and Et3N to produce amide (VI).Subsequent hydrogenation of the olefinic double bond of (VI) over Pd/C provided the target benzylthiazolidine.
合成路线:2) An alternative method starting from aniline (VII) employed the Meerwein arylation of methyl acrylate (IX) with the intermediate diazonium salt (VIII) in the presence of cuprous oxide.The resulting bromoester (X) was cyclized with thiourea (XI) in Et2O,followed by hydrolysis with HCl in sulfolane to afford (XIII).Finally,acid (XIII) was coupled to benzylamine (V) in the presence of (EtO)2POCN and Et3N.
📌 参考资料/链接:
参考文献标题:(3-Substituted benzyl)thiazolidine-2,4-diones as structurally new antihyperglycemic agents
文献作者:Nomura,M.; Kinoshita,S.; Satoh,H.; Maeda,T.; Murakami,K.; Tsunoda,M.; Miyachi,H.; Awano,K.
参考来源:Bioorg Med Chem Lett 1999,9(4),533