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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 9777생성일: 2026년 10월 26일

Pyridine → 3'-{({2-[4-(Aminosulfonyl)phenyl]ethyl}[(benzyloxy)acetyl]amino)methyl}-N-[2-(1-pyrrolidinyl)ethyl][1,1'-biphenyl]-3-carboxamide

https://huagongshe.com/reaction/9777

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물Benzyloxyacetyl chlorideHCID 177085—
반응물3'-[{2-[4-(aminosulfonyl)phenyl]ethyl}aminomethyl]-N-[2-(1-pyrrolidinyl)ethyl][1,1'-biphenyl]-3-carboxamideHCID 10239248—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물3'-{({2-[4-(Aminosulfonyl)phenyl]ethyl}[(benzyloxy)acetyl]amino)methyl}-N-[2-(1-pyrrolidinyl)ethyl][1,1'-biphenyl]-3-carboxamideHCID 10283122—

반응 단계

Pyridine (0.16 ml) and benzyloxyacetyl chloride (0.16 ml) were added to a solution of 3′-[{2-[4-(aminosulfonyl)phenyl]ethyl}aminomethyl]-N-[2-(1-pyrrolidinyl)ethyl]-[1,1′-biphenyl]-3-carboxamide (506 mg) in DMF (10 ml). The reaction mixture was stirred at room temperature for 16 hours, then diluted with water and extracted with ethyl acetate. The extract was washed with brine and dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The residues were purified by silica gel column chromatography (dichloromethane/methanol=98/2), whereby the title compound (257 mg) was obtained.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07091247B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-d4cc21a4adb5481cb9c9581135c634cc
출처 메모uspto-grants-2006_08