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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2047382생성일: 2026년 10월 26일

Acetic Acid → 2-[5-(4-Azepan-1-yl-piperidin-1-yl)-2-chloro-phenyl]-1H-benzoimidazole

https://huagongshe.com/reaction/2047382

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물AzepaneHCID 8119—
반응물Sodium triacetoxyborohydrideHCID 5049666—
반응물1-[3-(1H-benzo[d]imidazol-2-yl)-4-chlorophenyl]piperidin-4-oneHCID 59568243—
용매DichloromethaneHCID 6344—
생성물2-[5-(4-Azepan-1-yl-piperidin-1-yl)-2-chloro-phenyl]-1H-benzoimidazoleHCID 4412412058%

반응 단계

To a suspension of 1-[3-(1H-benzoimidazol-2-yl)-4-chloro-phenyl]-piperidin-4-one (0.10 g, 0.31 mmol) in dichloromethane (2 mL) was added azepane (0.05 mL, 0.46 mmol). After 30 min stirring at room temperature a drop of acetic acid was added, and after 1 h a further aliquot of azepane (0.05 mL, 0.46 mmol) was added, followed by sodium triacetoxyborohydride (NaB(OAc)3H) (0.10 g, 0.46 mmol). The reaction mixture was stirred at room temperature overnight, then the solvent was removed under reduced pressure, and the crude product dissolved in dichloromethane (10 mL). To the solution PS-isocyanate resin (PS-NCO) (Argonaut, loading 0.93 mmol/g) was added, then the mixture was shaken at room temperature overnight and filtered. The solvent was removed under reduced pressure to obtain a solid residue that was washed with EtOAc and Et2O then dried to give the desired product (0.07 g, 58%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08592463B2
출처 데이터셋uspto-grants-2013_11
ORD IDord-c92a700be4a84b15b19ba1d6ccec95b2
출처 메모uspto-grants-2013_11