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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2306295생성일: 2026년 10월 27일

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

https://huagongshe.com/reaction/2306295

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물2-AminobenzimidazoleHCID 13624—
반응물Benzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphateHCID 151348—
반응물3-cyclopentyl-2-(3,4-dichlorophenyl)propanoic AcidHCID 2762725—
용매WaterHCID 962—
용매DichloromethaneHCID 6344—
생성물N-(1H-benzimidazol-2-yl)-3-cyclopentyl-2-(3,4-dichloro-phenyl)-propionamideHCID 1017921695%

반응 조건

온도25 °C

반응 단계

A solution of 3-cyclopentyl-2-(3,4-dichlorophenyl)-propionic acid (prepared as in Example 1, 0.300 g, 1.04 mmol), benzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphate (0.707 g, 1.60 mmol), and 2-aminobenzimidazole (0.213 g, 1.6 mmol) in methylene chloride (10 mL) at 25° C. was treated with triethylamine (0.45 mL, 3.2 mmol). The reaction mixture was stirred at 25° C. for 16 h. The reaction mixture was then diluted with water (20 mL) and extracted with methylene chloride (3×10 mL). The combined organic layers were dried over sodium sulfate, filtered, and concentrated in vacuo. Flash chromatography (Merck Silica gel 60, 230-400 mesh, 80/20 hexanes/ethyl acetate) afforded N-(1H-benzoimidazol-2-yl)-3-cyclopentyl-2-(3,4-dichloro-phenyl)-propionamide (0.396 g, 95%) as a white solid: mp 193.4-196.8° C.; EI-HRMS m/e calcd for C21H21Cl2N3O (M+) 401.1062, found 401.1058.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06441184B1
출처 데이터셋uspto-grants-2002_08
ORD IDord-4fce0af6416f44fa85d4f89f5b2f9848
출처 메모uspto-grants-2002_08