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HRID 634573作成日:2026年10月25日

Sodium Hydroxide → 10-(2,3,4-Trihydroxybutyl)-1,4,7-triscarboxymethyl-1,4,7,10-tetraazacyclododecane

https://huagongshe.com/reaction/634573

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium HydroxideHCID 14798—
反応物1,4,7-Tris(carboxymethyl)-1,4,7,10-tetraazacyclododecaneHCID 107830—
反応物2,2-Dimethyl-4-(oxiran-2-YL)-1,3-dioxolaneHCID 13186827—
溶媒WaterHCID 962—
溶媒1,4-DioxaneHCID 31275—
生成物10-(2,3,4-Trihydroxybutyl)-1,4,7-triscarboxymethyl-1,4,7,10-tetraazacyclododecaneHCID 10694842—

反応手順

10.0 g (28.87 mmol) of 1,4,7-triscarboxymethyl-1,4,7,10-tetraazacyclododecane (DO3A) is dissolved in 40 ml of water, and the pH is set at 13 with 5N sodium hydroxide solution. A solution of 6.24 g (43.30 mmol) of 2-(2,2-dimethyl-1,3-dioxolan-4-yl)ethylene oxide (DE 3,150,917) in 10 ml of dioxane is added thereto, and the mixture is stirred for 24 hours at room temperature. The mixture is diluted with 60 ml of water and extracted three times with 50 ml of ether. The aqueous phase is brought to pH 2 with 10% strength hydrochloric acid and evaporated. The residue is dissolved in a small amount of water and passed to a cation exchange column (IR 120). After flushing with water, the ligand is eluted with 0.5-normal aqueous ammonia solution. The fractions are evaporated, the ammonium salt is taken up in a small amount of water and passed over an anion exchange column (IRA 67). The mixture is first washed with water and then eluted with 0.5-normal aqueous formic acid. The product is evaporated under vacuum, the residue is dissolved in a small amount of hot methanol, and acetone is added, thus crystallizing the title compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06183724B2
出典データセットuspto-grants-2001_02
ORD IDord-d142290e28a6405cb27515146ac384c5
出典メモuspto-grants-2001_02