Cummins C H, Rutter E W, Fordyce W A
Dow Chemical Company, Midland, Michigan 48674.
Bioconjug Chem. 1991 May-Jun;2(3):180-6. doi: 10.1021/bc00009a007.
The bifunctional chelating agents N,N,N',N'',N''-pentakis(carboxymethyl)-1- [(4-aminophenyl)methyl]-diethylenetriamine and N,N,N',N'',N''-pentakis(carboxymethyl)-1-[(4-aminophenyl)methyl]-4- methyldiethylenetriamine were prepared in six-step syntheses in overall yields of 38% and 31%, respectively. The use of bromoacetate esters in the synthesis allowed large-scale flash chromatographic purification of reaction products. The synthesis of N,N,N',N'',N''-pentakis(carboxymethyl)-1- [(4-aminophenyl)-methyl]-4-methyldiethylenetriamine resulted in a mixture of two diastereomers. Chelation of yttrium-(III) with these bifunctional chelating agents resulted in 1:1 chelates. In the case of N,N,N',N'',N''-pentakis(carboxymethyl)-1-[4- aminophenyl)methyl]diethylenetriamine, two diastereomers were observed upon chelation, as expected. In the case of N,N,N',N'',N''- pentakis(carboxymethyl)-1-[(4-aminophenyl)-methyl]-4- methyldiethylenetriamine, only three of the four anticipated diastereomers were observed.
双功能螯合剂N,N,N',N'',N''-五(羧甲基)-1-[(4-氨基苯基)甲基]-二亚乙基三胺和N,N,N',N'',N''-五(羧甲基)-1-[(4-氨基苯基)甲基]-4-甲基二亚乙基三胺通过六步合成法制备,总产率分别为38%和31%。在合成中使用溴乙酸酯可对反应产物进行大规模快速柱色谱纯化。N,N,N',N'',N''-五(羧甲基)-1-[(4-氨基苯基)甲基]-4-甲基二亚乙基三胺的合成产生了两种非对映异构体的混合物。钇(III)与这些双功能螯合剂螯合生成1:1螯合物。对于N,N,N',N'',N''-五(羧甲基)-1-[(4-氨基苯基)甲基]二亚乙基三胺,螯合时观察到两种非对映异构体,正如预期的那样。对于N,N,N',N'',N''-五(羧甲基)-1-[(4-氨基苯基)甲基]-4-甲基二亚乙基三胺,只观察到了四种预期非对映异构体中的三种。