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HRID 9774作成日:2026年10月24日

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

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

反応式

関与物質

役割名称HCID仕込み量
反応物4-(2-Aminoethyl)benzenesulfonamideHCID 169682—
反応物3'-formyl-N-[2-(1-pyrrolidinyl)ethyl][1,1'-biphenyl]-3-carboxamideHCID 21987320—
溶媒MethanolHCID 887—
溶媒TetrahydrofuranHCID 8028—
生成物3'-[{2-[4-(aminosulfonyl)phenyl]ethyl}aminomethyl]-N-[2-(1-pyrrolidinyl)ethyl][1,1'-biphenyl]-3-carboxamideHCID 10239248—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07091247B2
出典データセットuspto-grants-2006_08
ORD IDord-c113ed0e9c5f49ae997f36f353ec3220
出典メモuspto-grants-2006_08