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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1280038생성일: 2026년 10월 24일

Triethylamine → N-(1H-benzimidazol-2-yl)-2-(3-bromo-4-methanesulfonyl-phenyl)-3-cyclopentyl-propionamide

https://huagongshe.com/ko/reaction/1280038

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물2-AminobenzimidazoleHCID 13624—
반응물Benzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphateHCID 151348—
반응물2-(3-Bromo-4-methanesulfonyl-phenyl)-3-cyclopentyl-propionic acidHCID 12067666—
용매DichloromethaneHCID 6344—
생성물N-(1H-benzimidazol-2-yl)-2-(3-bromo-4-methanesulfonyl-phenyl)-3-cyclopentyl-propionamideHCID 1027807653%

반응 단계

A solution of 2-(3-bromo-4-methanesulfonyl-phenyl)-3-cyclopentyl-propionic acid (100 mg, 0.266 mmol), triethylamine (110 μL, 0.80 mmol), benzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphate (187 mg, 0.42 mmol), and 2-aminobenzimidazole (56 mg, 0.42 mmol) in methylene chloride (10 mL) was stirred at 25° C. for 1.5 h. The reaction mixture was partitioned between water and methylene chloride. The organic layer was washed sequentially with a 1N aqueous hydrochloric acid solution (1×mL), water (1×10 mL), and a saturated aqueous sodium bicarbonate solution (1×10 mL). The organic layer was then dried over magnesium sulfate, filtered, and concentrated in vacuo. Biotage chromatography (FLASH 40S, Silica, 19/1 chloroform/methanol) afforded N-(1H-benzoimidazol-2-yl)-2-(3-bromo-4-methanesulfonyl-phenyl)-3-cyclopentyl-propionamide (69 mg, 53%) as a white solid: mp>220° C.; EI-HRMS m/e calcd for C22H24BrN3O3S (M+) 489.0722, found 489.0727.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06448399B1
출처 데이터셋uspto-grants-2002_09
ORD IDord-6a169bc1fff1420a9e60ee274c1e39a0
출처 메모uspto-grants-2002_09