新产品编号:1569853
Chemical Name: N-Cyclohexyl-N-methyl-L-leucyl-4-O-(benzyl)-L-tyrosine tert-butylamide
项目整合开发状态: Preclinical
项目研究机构: Elan (Originator), Pfizer (Originator)
合成路线:Coupling of N-Boc-O-benzyl-L-tyrosine (I) with tert-butylamine by means of O-benzotriazol-1-yl-N,N,N',N'-tetramethyluronium hexafluorophosphate (HBTU) afforded amide (II).Subsequent acid cleavage of the Boc group of (II) gave O-benzyltyrosine tert-butyl amide (III).
合成路线:N-Methyl-L-leucine (IV) was converted to tert-butyl ester (V) by treatment with isobutylene and H2SO4.Formation of the N,N-dialkyl derivative (VIII) was achieved by either alkylation of (V) with p-tert-butylbenzyl bromide (VI) or by reductive condensation of (V) with p-tert-butylbenzaldehyde (VII) and NaBH(OAc)3.Deprotection of the tert-butyl ester of (VIII) with trifluoroacetic acid gave amino acid (IX),which was activated as the mixed anhydride (X) upon treatment with isobutyl chloroformate and a polymer-supported morpholine base.Coupling of (X) with tyrosine amide (III) then afforded the title dipeptide amide.Unreacted starting materials were captured by the addition of polymer-supported polyamine and isocyanate resins.
合成路线:The precursor amino acid derivatives were obtained as follows:The condensation of N-Boc-O-benzyltyrosine (I) with tert-butylamine using O-benzotriazol-1-yl-N,N,N',N'-tetramethyluronium hexafluorophosphate (HBTU) gave amide (II).Subsequent deprotection of the Boc group of (II) by means of trifluoroacetic acid provided O-benzyltyrosine tert-butyl amide (III).N-Methyl leucine benzyl ester (IV) was alkylated with 3-bromocyclohexene (V),yielding the cyclohexenyl amine (VI).Hydrogenation of the olefinic double bond of (VI) with concomitant benzyl ester hydrogenolysis in the presence of Pd/C furnished N-cyclohexyl-N-methylleucine (VII).The title dipeptide was finally obtained by HBTU-promoted coupling of amino acids (III) and (VII).
合成路线:Alternatively,the compound was prepared using polymer-supported resins.Dialkyl leucine (VII) was first treated with isobutyl chloroformate and morpholine resin,tyrosine derivative (III) was added,and was then treated with isocyanate resin and tris(2-aminomethyl)amine resin.Filtration of the insoluble resins provided a solution of pure dipeptide derivative.
📌 参考资料/链接:
参考文献标题:Substd.peptidylamine calcium channel blockers
文献作者:Szoke,B.G.; Rafferty,M.F.; Silva,D.F.; Song,Y.; Malone,T.C.; Hu,L.-Y.; Urge,L.; Nadasdi,L.; Ryder,T.R.(Neurex Corp.; Pfizer Inc.)
参考来源:WO 9854123
📄 详细内容
合成路线:The precursor amino acid derivatives were obtained as follows:The condensation of N-Boc-O-benzyltyrosine (I) with tert-butylamine using O-benzotriazol-1-yl-N,N,N',N'-tetramethyluronium hexafluorophosphate (HBTU) gave amide (II).Subsequent deprotection of the Boc group of (II) by means of trifluoroacetic acid provided O-benzyltyrosine tert-butyl amide (III).N-Methyl leucine benzyl ester (IV) was alkylated with 3-bromocyclohexene (V),yielding the cyclohexenyl amine (VI).Hydrogenation of the olefinic double bond of (VI) with concomitant benzyl ester hydrogenolysis in the presence of Pd/C furnished N-cyclohexyl-N-methylleucine (VII).The title dipeptide was finally obtained by HBTU-promoted coupling of amino acids (III) and (VII).
参考文献标题:N,N-dialkyl-dipeptidylamines as novel N-type calcium channel blockers
文献作者:Hu,L.-Y.; Ryder,T.R.; Rafferty,M.F.; Cody,W.L.; Lotarski,S,M.; Miljanich,G.P.; Millerman,E.; Rock,D.M.; Song,Y.; Stoehr,S.J.; Taylor,C.P.; Weber,M.l.; Szoke,B.G.; Vartanian,M.G.
参考来源:Bioorg Med Chem Lett 1999,9(6),907