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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 15546생성일: 2026년 10월 23일

1-Chloro-4-(chloromethyl)benzene → {5-[(4-Chloro-benzyl)-(4-fluoro-benzenesulfonyl)-amino]-2-propyl-benzoimidazol-1-yl}-acetic acid tert-butyl ester

https://huagongshe.com/ko/reaction/15546

반응식

참여 물질

역할이름HCID투입량
반응물1-Chloro-4-(chloromethyl)benzeneHCID 7723—
반응물Potassium CarbonateHCID 11430—
반응물[5-(4-Fluoro-benzenesulfonylamino)-2-propyl-benzoimidazol-1-yl]-acetic acid tert-butyl esterHCID 67201670—
용매WaterHCID 962—
용매AcetonitrileHCID 6342—
용매Ethyl AcetateHCID 8857—
생성물{5-[(4-Chloro-benzyl)-(4-fluoro-benzenesulfonyl)-amino]-2-propyl-benzoimidazol-1-yl}-acetic acid tert-butyl esterHCID 67199541—

반응 조건

온도80 °C

반응 단계

4-Chlorobenzyl chloride (0.27 mmol) and K2CO3 (63 mg, 0.45 mmol) were added to a solution of [5-(4-fluoro-benzenesulfonylamino)-2-propyl-benzoimidazol-1-yl]-acetic acid tert-butyl ester (40 mg, 0.09 mmol) in CH3CN (1 mL), and stirred overnight at 80° C. The reaction mixture was diluted with EtOAc and H2O, and then filtered through an Extrelut column. The column was washed with EtOAc, and the filtrate was concentrated. The crude product was carried onto the next reaction without any further purification or characterization.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07732618B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-f15124e661274eb8982f6080f0da4c3e
출처 메모uspto-grants-2010_06