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HRID 37050作成日:2026年10月23日

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

https://huagongshe.com/ja/reaction/37050

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium IodideHCID 5238—
反応物TriethylamineHCID 8471—
反応物2-(Chloroethoxy)ethanolHCID 12361—
反応物Tri-tert-butyl 1,4,7,10-Tetraazacyclododecane-1,4,7-triacetateHCID 11237632—
溶媒DimethylformamideHCID 6228—
生成物1-(5-Hydroxy-3-oxapentyl)-1,4,7,10-tetraazacyclododecane-4,7,10-triacetic acidHCID 19438545—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05419893
出典データセットuspto-grants-1995_05
ORD IDord-a09a9c54bb3348709006ef40b418f2b8
出典メモuspto-grants-1995_05