Реакция #563971

ord-6a459e667aea4980ac5a3116568f6d5d

Уравнение реакции

[H][H]
hydrogen
C1CNCCNCCNCCN1
1,4,7,10-tetraazacyclododecane
c1ccccc1
benzene
CCCCCCCCCCCCC
tridecane

Реагенты

Нет

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ДругоеA preferred preparation of the compounds of formula I wherein Y

Методика

A preferred preparation of the compounds of formula I wherein Y is NH and R2 is hydrogen is to react 1,4,7,10-tetraazacyclododecane, known in the art, with dimethylformamidedimethylacetal in the presence of benzene to yield 1,4,7,10-tetraazatricyclo[5.5.1.0]tridecane. This "tricyclic" compound is reacted with an ethanol/water mixture to yield 1-formyl-1,4,7,10-tetraazacyclododecane. This formyl compound is then reacted with t-butyl bromoacetate to yield 1-formyl, 4,7,10-triscarboxymethyl-1,4,7,10-tetraazacyclododecane, tris-t-butylester. Finally, the ester groups are removed in the presence of strong acid, such as sulfuric acid, to yield a compound of formula I wherein Y is NH and R2 is hydrogen.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US04885363uspto-grants-1989_12