Реакция #65328

Уравнение реакции

1,4,7,10-Tetraazacyclododecane-4,7,10-triacetic acid tri-t-butyl-ester

Sodium iodide

triethylamine

2(2-chloroethoxy) ethanol

→

title compound

1-(5-Hydroxy-3-oxapentyl)-1,4,7,10-tetraazacyclododecane-4,7,10-triacetic acid

Растворители

dimethylformamide

Условия реакции

Обработка

1. 1
   ТемператураThe temperature was then raised to 100° C.
2. 2
   workup.WAITkept there for 1 hour
3. 3
   ДругоеThe solvent was then evaporated
4. 4
   workup.DISSOLUTIONthe residue dissolved in a mixture of dichloromethane (4.5 ml) and trifluoroacetic acid (4.5 ml)
5. 5
   workup.STIRRINGThe mixture was stirred for 2 hours at ambient temperature
6. 6
   Другоеthe solvent was then evaporated
7. 7
   workup.DISSOLUTIONThe residue was dissolved in water (8 ml)
8. 8
   Промывкаthis aqueous solution was washed with ether (6×4 ml)

Методика

1,4,7,10-Tetraazacyclododecane-4,7,10-triacetic acid tri-t-butyl-ester (515 mg, 1 mmol) was dissolved in dimethylformamide (3 ml). Sodium iodide (15 mg, 0.1 mmol), triethylamine (233 mg, 2.5 mmol) and 2(2-chloroethoxy) ethanol (313 mg, 3.5 mmol) were added to the stirred mixture at ambient temperature. The mixture was stirred for 18 hours at ambient temperature. The temperature was then raised to 100° C. and kept there for 1 hour. The solvent was then evaporated and the residue dissolved in a mixture of dichloromethane (4.5 ml) and trifluoroacetic acid (4.5 ml). The mixture was stirred for 2 hours at ambient temperature and the solvent was then evaporated. The residue was dissolved in water (8 ml), and this aqueous solution was washed with ether (6×4 ml). The aqueous solution was acidified and the title compound was isolated as a hygroscopic white powder after evaporation of the water. Yield 325 mg (75%), FAB MS: 435(M+1 ). The structure was confirmed by 1HNMR and 13C NMR.

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