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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1434680생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1434680

반응식

참여 물질

역할이름HCID투입량
반응물BenzimidazoleHCID 5798—
반응물TriphenylphosphineHCID 11776—
반응물4-bromo-N-(1,3-thiazol-2-yl)benzene-1-sulfonamideHCID 669304—
촉매Copper iodideHCID 83717—
촉매palladium(II) acetateHCID 167845—
용매AcetoneHCID 180—
용매1,4-DioxaneHCID 31275—
생성물4-(1H-Benzimidazol-2-yl)-N-(1,3-thiazol-2-yl)benzene-1-sulfonamideHCID 160399332.2%

반응 조건

온도150 °C

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07615569B2
출처 데이터셋uspto-grants-2009_11
ORD IDord-11b19ce5401e465389a45aed940ef3c2
출처 메모uspto-grants-2009_11