戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 13449作成日:2026年10月25日

Tert-butyl 4-{2-[(4-bromophenyl)amino]-1-methylbenzimidazol-5-yloxy}pyridine-2-carboxylate → 4-{2-[(4-Bromophenyl)amino]-1-methylbenzimidazol-5-yloxy}pyridine-2-carboxylic acid

https://huagongshe.com/reaction/13449

反応式

関与物質

役割名称HCID仕込み量
反応物Tert-butyl 4-{2-[(4-bromophenyl)amino]-1-methylbenzimidazol-5-yloxy}pyridine-2-carboxylateHCID 22041284—
触媒WaterHCID 962—
溶媒Trifluoroacetic acidHCID 6422—
生成物4-{2-[(4-Bromophenyl)amino]-1-methylbenzimidazol-5-yloxy}pyridine-2-carboxylic acidHCID 22040646—

反応手順

A solution of the product of step 7 in trifluoroacetic acid was treated with two drops of water at room temperature for 3-4 hours or until the reaction was determined to be complete by HPLC. The reaction was evaporated under reduced pressure to afford the product as a red-orange oil in quantitative yield. MS: MH+=439.

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-33af28af016b497fa6bf2bf439a5eae2
出典メモuspto-grants-2010_06