摘要
在KOH存在下,1,4,7,10-四氮杂环十二烷与溴乙酸发生N-羧甲基化反应,得N,N’,N”,N-四乙酸-1,4,7,10-四氮杂环十二烷(DOTA,1),产率88.1%。在K2CO3作用下,1,4,8,11-四氮杂环+四烷与溴乙酸苄酯进行反应,得N-乙酸苄酯衍生物,经Pd/C催化氢解生成N,N’,N”,N-四乙酸-1,4,8,11-四氮杂环十四烷(TETA,3),产率56.0%。DOTA和TETA分别与LaCl3和GdCl3形成络合物,产率为64.1%~74.6%。
Tetraazacy clododecane-N, N', N', N,tetraacetic acid(DOTA, 1) was synthesized by N-carboxylmethylation of 1, 4, 7, 10-tetraazacyclododecane with bromoacetic acid in the presence of potassium hydroxide. The yield was 88. 1 %. 1, 4, 8, 11-Tetraazacyclotetradecane-N,N',N', N-tetraacetic acid (TETA,3) was synthesized by the hydrogenolysis of N-benzylacetate of tetraaza macrocylic alkane which was prepared by the alkylation of 1, 4, 8, 11-tetraazacyclotetradecane with benzyl 2-bromoacetate in the presence of potassium carbonate. The yield of 3 was56. 0%. Four lanthanide complexes with a tetraacetic tetraaza macrocyclic alkane were obtained from the reactions of 1 and/or 3 with LaCl3 and/or GdCl3. The yields were 64. 1 %~74. 6 %.
出处
《化学试剂》
CAS
CSCD
北大核心
1996年第3期168-170,共3页
Chemical Reagents
关键词
DOTA
氮杂环烷烃
镧
钆
配合物
tetraazacy clododecane, 1, 4, 7, 10-tetraazacy clododecane-N, N', N', N-tetraacetie acid,1, 4, 8, 11-tetraazacy clotetra decane, 1, 4, 8, 11-tetra azacyclotetradecane-N,N',N',N-tetraacetic acid