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HRID 412331作成日:2026年10月25日

Phenyl Isothiocyanate → 1-(4-[2-[4-(2,4-Dioxothiazolidin-5-ylmethyl)phenoxymethyl]-1-methyl-1H-benzimidazol-6-yloxy]phenyl)-3-(phenyl)thiourea

https://huagongshe.com/reaction/412331

反応式

関与物質

役割名称HCID仕込み量
反応物Phenyl IsothiocyanateHCID 7673—
反応物TriethylamineHCID 8471—
反応物5-[4-[6-(4-aminophenoxy)-1-methyl-1H-benzimidazol-2-ylmethoxy]benzyl]thiazolidine-2,4-dione dihydrochlorideHCID 86587768—
溶媒DimethylformamideHCID 6228—
生成物1-(4-[2-[4-(2,4-Dioxothiazolidin-5-ylmethyl)phenoxymethyl]-1-methyl-1H-benzimidazol-6-yloxy]phenyl)-3-(phenyl)thioureaHCID 1853759177.9%

反応手順

A mixture of 5-[4-[6-(4-aminophenoxy)-1-methyl-1H-benzimidazol-2-ylmethoxy]benzyl]thiazolidine-2,4-dione dihydrochloride (400 mg), phenyl isothiocyanate (113 mg), triethylamine (153 mg) and anhydrous N,N-dimethylformamide (8 ml) was stirred at room temperature for 4 hours. 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 recrystallized from a mixture of ethanol and ethyl acetate (5:1) to afford the title compound (347 mg, mp 129.6-130.9° 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-3d9d89e04707430088eccd68f7ce8a82
出典メモuspto-grants-2003_05