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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 9774생성일: 2026년 10월 24일

4-(2-Aminoethyl)benzenesulfonamide → 3'-[{2-[4-(aminosulfonyl)phenyl]ethyl}aminomethyl]-N-[2-(1-pyrrolidinyl)ethyl][1,1'-biphenyl]-3-carboxamide

https://huagongshe.com/ko/reaction/9774

반응식

참여 물질

역할이름HCID투입량
반응물4-(2-Aminoethyl)benzenesulfonamideHCID 169682—
반응물3'-formyl-N-[2-(1-pyrrolidinyl)ethyl][1,1'-biphenyl]-3-carboxamideHCID 21987320—
용매MethanolHCID 887—
용매TetrahydrofuranHCID 8028—
생성물3'-[{2-[4-(aminosulfonyl)phenyl]ethyl}aminomethyl]-N-[2-(1-pyrrolidinyl)ethyl][1,1'-biphenyl]-3-carboxamideHCID 10239248—

반응 단계

4-(2-Aminoethyl)benzene sulfonamide (2.37 g) and molecular sieves 3A (4.0 g) were added to a solution of 3′-formyl-N-[2-(1-pyrrolidinyl)ethyl][1,1′-biphenyl]-3-carboxamide (3.81 g) in methanol (50 ml), and the mixture was stirred at room temperature for 1.5 hours. After the reaction mixture was diluted with tetrahydrofuran (THF), the molecular sieves were filtered off, and the filtrate was concentrated under reduced pressure. The residues were dissolved in a mixed solvent (100 ml) of methanol-THF (1:1), and sodium borohydride (0.89 g) was added thereto. The reaction mixture was stirred at room temperature for 5 hours, and then the solvent was evaporated under reduced pressure. The residues were diluted with water and extracted with ethyl acetate. The extract was washed with brine and then dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The residues were crystallized from hexane, whereby the title compound (3.71 g) was obtained.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07091247B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-c113ed0e9c5f49ae997f36f353ec3220
출처 메모uspto-grants-2006_08