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HRID 412345作成日:2026年10月25日

1,3-Benzodioxole-5-carboxylic acid → 1-(Benzo[1,3]dioxol-5-yl)-3-(3-[2-[4-(2,4-dioxothiazolidin-5-ylmethyl)phenoxymethyl]-1-methyl-1H-benzimidazol-6-yloxy]phenyl)urea

https://huagongshe.com/reaction/412345

反応式

関与物質

役割名称HCID仕込み量
反応物1,3-Benzodioxole-5-carboxylic acidHCID 7196—
反応物TriethylamineHCID 8471—
反応物P,P-Diphenylphosphinic azideHCID 199401—
反応物5-[4-[6-(3-aminophenoxy)-1-methyl-1H-benzimidazol-2-ylmethoxy]benzyl]thiazolidine-2,4-dione dihydrochlorideHCID 86587772—
溶媒TolueneHCID 1140—
溶媒DimethylformamideHCID 6228—
生成物1-(Benzo[1,3]dioxol-5-yl)-3-(3-[2-[4-(2,4-dioxothiazolidin-5-ylmethyl)phenoxymethyl]-1-methyl-1H-benzimidazol-6-yloxy]phenyl)ureaHCID 185376245.6%

反応条件

温度80 °C

反応手順

A mixture of piperonylic acid (133 mg), diphenylphosphoryl azide (217 mg), triethylamine (314 mg) and anhydrous toluene (8 ml) was stirred at 80° C. for 1 hour. To the reaction mixture was added 5-[4-[6-(3-aminophenoxy)-1-methyl-1H-benzimidazol-2-ylmethoxy]benzyl]thiazolidine-2,4-dione dihydrochloride (400 mg) and anhydrous N,N-dimethylformamide (4 ml) at room temperature and the mixture was stirred at the same temperature for 1 hour and then allowed to stand overnight. The reaction mixture was concentrated and partitioned between ethyl acetate and water. The extract was washed with saturated aqueous sodium chloride solution, dried over anhydrous sodium sulfate and then concentrated. The residue was chromatographed on a silica gel column using ethyl acetate:n-hexane=3:1→1:0 as the eluant. The product insoluble in a mixture of methanol and diisopropyl ether (5:1) was isolated by filtration and was further purified by preparative reverse phase high performance liquid chromatography using acetonitrile/water=50:50 as the eluant to afford the title compound (26 mg, mp 179.2-182.4° C.).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06562849B1
出典データセットuspto-grants-2003_05
ORD IDord-b0c11f8d08bc412984da50e755ff0134
出典メモuspto-grants-2003_05