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HRID 13504作成日:2026年10月24日

Methyl iodide → Methyl5-{2-[(4-bromophenyl)amino]-1-methylbenzimidazol-5-yloxy}pyridine-3-carboxylate

https://huagongshe.com/ja/reaction/13504

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl iodideHCID 6328—
反応物4-Bromophenyl isothiocyanateHCID 16133—
反応物Methyl5-[3-amino-4-(methylamino)phenoxy]pyridine-3-carboxylateHCID 22040511—
溶媒MethanolHCID 887—
生成物Methyl5-{2-[(4-bromophenyl)amino]-1-methylbenzimidazol-5-yloxy}pyridine-3-carboxylateHCID 22040538—

反応手順

A solution of the methyl5-[3-amino-4-(methylamino)phenoxy]pyridine-3-carboxylate (1 eq) in methanol (8 ml) was treated with 4-bromophenylisothiocyanate (1 eq) and stirred at 60° C.-65° C. for 2 hours. The reaction mixture was cooled down to room temperature and methyl iodide (1 eq) was added and stirred overnight at 60° C. The reaction was cooled down to room temperature, evaporated, taken up in ethyl acetate and washed with water and brine, dried, evaporated under reduced pressure. Column chromatography yielded methyl5-{2-[(4-bromophenyl)amino]-1-methylbenzimidazol-5-yloxy}pyridine-3-carboxylate. MS: MH+=452

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07728010B2
出典データセットuspto-grants-2010_06
ORD IDord-1b337a0935334edbab9388c479de6e9a
出典メモuspto-grants-2010_06