新产品编号:829477

Chemical Name: 5-(3',5'-Di-tert-butyl-2'-propoxybiphenyl-2-yl)-3-methyl-2,4-pentadienoic acid sodium salt
CAS No. 331248-51-2 (free acid)
项目整合开发状态: Preclinical
项目研究机构: Ligand (Originator), Lilly (Originator)
合成路线:Addition of methyllithium to 3,5-di-tert-butylsalicylic acid (I) affords ketone (II).Wittig condensation of the ortho-hydroxyacetophenone (II) with (carbethoxymethylene)triphenylphosphorane leads to the coumarin derivative (III).Subsequent reductive opening of the lactone ring of (III) by means of LiAlH4 provides diol (IV).The phenolic hydroxyl of (IV) is then alkylated by 1,1-difluoro-2-bromoethane (V) in the presence of CsF to furnish the difluoroethyl ether (VI).Oxidation of the allylic alcohol function of (VI) to aldehyde (VII) is accomplished by treatment with tetrapropylammonium perruthenate and N-methylmorpholine-N-oxide.Wadsworth-Emmons condensation of the unsaturated aldehyde (VII) with phosphonate (VIII) then provides the triene adduct (IX).The ethyl ester group of (IX) is finally hydrolyzed under alkaline conditions to the desired carboxylic acid.

合成路线:Alkylation of 2,4-di-tert-butyl-6-iodophenol (I) with bromopropane by means of NaH (1) or CsF (2) provides the corresponding propyl ether (II).Subsequent Suzuki coupling of aryl iodide (II) with 2-formylbenzeneboronic acid (III) leads to the biphenyl aldehyde (IV).This is then condensed with phosphonate (V) producing the dienoate ester (VI).Finally,the ethyl ester group of (VI) is hydrolyzed with LiOH to the target carboxylic acid (1,2).
📌 参考资料/链接:
参考文献标题:RXR modulators with improved pharmacologic profile
文献作者:Jones,T.K.; Ardecky,R.J.; Boehm,M.F.; Hamann,L.G.; Thompson,A.J.; Michellys,P.-Y.; Tyhonas,J.S.; Faulkner,A.L.; Mapes,C.M.; Chen,J.-H.(Ligand Pharmaceuticals,Inc.)
参考来源:EP 1216221; WO 0119770

📄 详细内容


合成路线:Alkylation of 2,4-di-tert-butyl-6-iodophenol (I) with bromopropane by means of NaH (1) or CsF (2) provides the corresponding propyl ether (II).Subsequent Suzuki coupling of aryl iodide (II) with 2-formylbenzeneboronic acid (III) leads to the biphenyl aldehyde (IV).This is then condensed with phosphonate (V) producing the dienoate ester (VI).Finally,the ethyl ester group of (VI) is hydrolyzed with LiOH to the target carboxylic acid (1,2).
参考文献标题:RXR modulators.Design and synthesis of new RXR-selective phenyl- and pyridine-locked dienoic acids for the treatment of type 2 diabetes
文献作者:Chen,J-H.; Michellys,P-Y.; Ardecky,R.J.; Tyhonas,J.S.; Leibowitz,M.D.; Liu,S.; Rungta,D.; D'Arrigo,J.; Mais,D.E.; Miller,A.; Grese,T.A.; Mapes,C.M.; Thompson,A.W.; Boehm,M.F.; Ogilvie,K.M.; Karanewsky,D.S.
参考来源:225th ACS Natl Meet (March 23 2003,New Orleans) 2003,Abst MEDI 262