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HRID 559500作成日:2026年10月27日

Benzimidazole → 4-(1H-Benzimidazol-2-yl)-N-(1,3-thiazol-2-yl)benzene-1-sulfonamide

https://huagongshe.com/reaction/559500

反応式

関与物質

役割名称HCID仕込み量
反応物BenzimidazoleHCID 5798—
反応物TriphenylphosphineHCID 11776—
反応物4-bromo-N-(1,3-thiazol-2-yl)benzene-1-sulfonamideHCID 669304—
触媒Copper iodideHCID 83717—
触媒palladium(II) acetateHCID 167845—
溶媒AcetoneHCID 180—
溶媒1,4-DioxaneHCID 31275—
生成物4-(1H-Benzimidazol-2-yl)-N-(1,3-thiazol-2-yl)benzene-1-sulfonamideHCID 160399332.2%

反応条件

温度150 °C

反応手順

Benzimidazole (0.313 mmol) and MgO (0.376 mmol) was stirred in 1,4-dioxane (2 mL) for 10 min. at room temp. To the solution, copper iodide (0.627 mmol), palladium acetate (0.016 mmol), triphenylphosphine (0.062 mmol), and 4-bromo-N-thiazol-2-yl-benzenesulfonamide (0.313 mmol) were added. The reaction was sealed and heated to 150° C. After 7 h the reaction was cooled to 120° C. and stirred overnight. The reaction was cooled to room temperature and diluted with acetone. The solution was filtered through Celite and concentrated in vacuo. The crude was purified by reverse phase chromatography to yield 4-(1H-benzoimidazol-2-yl)-N-thiazol-2-yl-benzenesulfonamide (0.007 mmol).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08063080B2
出典データセットuspto-grants-2011_11
ORD IDord-0edeac393455446c8c1f13128fb177e6
出典メモuspto-grants-2011_11