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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1614518생성일: 2026년 10월 26일

Sodium Iodide → 1-(3-Hydroxy-propyl)-1,4,7,10-tetraazacyclododecane-4,7,10-triacetic acid

https://huagongshe.com/reaction/1614518

반응식

참여 물질

역할이름HCID투입량
반응물Sodium IodideHCID 5238—
반응물TriethylamineHCID 8471—
반응물3-Chloro-1-propanolHCID 12313—
반응물Tri-tert-butyl 1,4,7,10-Tetraazacyclododecane-1,4,7-triacetateHCID 11237632—
용매DimethylformamideHCID 6228—
생성물1-(3-Hydroxy-propyl)-1,4,7,10-tetraazacyclododecane-4,7,10-triacetic acidHCID 19438511—

반응 단계

1,4,7,10-Tetraazacyclododecane-4,7,10-triacetic acid tri-t-butyl ester (360 mg, 0.70 mmol) (Example 22(a)) was dissolved in dimethylformamide (2.1 ml). Sodium iodide (15 mg, 1 mmol), triethylamine (142 mg, 1.4 mmol) and 3-chloro-1 propanol (132 mg, 1.4 mmol) were added to the stirred mixture at ambient temperature. The mixture was stirred for 3 hours at ambient temperature, the temperature was then raised to 100° C. and kept there for 2 hours. The solvent was evaporated and the residue was dissolved in dichloromethane (3 ml) and washed with water (1 ml). Trifluoroacetic acid (2 ml) was added to the dichloromethane solution and the mixture was stirred at ambient temperature for 1 hour. The solvents were evaporated and the residue dissolved in water (6 ml). The aqueous solution was washed with ether (6×3 ml). The aqueous solution was acidified, the water was evaporated, and the title compound was isolated as a hygroscopic white powder. Yield 192 mg (68%), FAB MS: 405(M+1). The structure was confirmed by 1HNMR and 13CNMR

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05198208
출처 데이터셋uspto-grants-1993_03
ORD IDord-646e2e55d02340b1bbb1f7fe1644cfde
출처 메모uspto-grants-1993_03