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HRID 1915693作成日:2026年10月25日

4-[2-(4-Fluoro-phenylamino)-1-methyl-1H-benzoimidazol-5-yloxy]-pyridine-2-carboxylic acid tert-butyl ester → 4-[2-(4-Fluoro-phenylamino)-1-methyl-1H-benzoimidazol-5-yloxy]-pyridine-2-carboxylic acid

https://huagongshe.com/reaction/1915693

反応式

関与物質

役割名称HCID仕込み量
反応物4-[2-(4-Fluoro-phenylamino)-1-methyl-1H-benzoimidazol-5-yloxy]-pyridine-2-carboxylic acid tert-butyl esterHCID 21037368—
触媒WaterHCID 962—
溶媒Trifluoroacetic acidHCID 6422—
生成物4-[2-(4-Fluoro-phenylamino)-1-methyl-1H-benzoimidazol-5-yloxy]-pyridine-2-carboxylic acidHCID 22041294—

反応手順

A stirring solution of 4-[2-(4-Fluoro-phenylamino)-1-methyl-1H-benzoimidazol-5-yloxy]-pyridine-2-carboxylic acid tert-butyl ester in trifluoroacetic acid was treated with two drops of water at room temperature for 3-4 hours or when the reaction was determined to be complete by HPLC. The reaction was evaporated under reduced pressure and then ether was added to the residue, which was then sonicated for 30 minutes. Filtration and washing with ether yields the desired acid in quantitative yield. LCMS m/z 379.4 (MH+), tR=1.74 mm.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08614330B2
出典データセットuspto-grants-2013_12
ORD IDord-2e43236960ea4cc1b265a047d7234db3
出典メモuspto-grants-2013_12