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HRID 607451作成日:2026年10月24日

1-[2-(2-Hydroxyethoxy)ethyl]piperazine → (S)-N-[(3-{4-[2-(2-hydroxyethoxy)ethyl]piperazin-1-yl}propyl)(oxido)phenyl--sulfanylidene]-5-({3-[(3-methyl-2-furoyl)amino]phenyl}ethynyl)nicotinamide

https://huagongshe.com/ja/reaction/607451

反応式

関与物質

役割名称HCID仕込み量
反応物1-[2-(2-Hydroxyethoxy)ethyl]piperazineHCID 139436—
反応物N-[(3-bromopropyl)(oxido)phenyl--sulfanylidene]-5-({3-[(3-methyl-2-furoyl)amino]phenyl}ethynyl)nicotinamideHCID 76585264—
溶媒DimethylformamideHCID 6228—
生成物(S)-N-[(3-{4-[2-(2-hydroxyethoxy)ethyl]piperazin-1-yl}propyl)(oxido)phenyl--sulfanylidene]-5-({3-[(3-methyl-2-furoyl)amino]phenyl}ethynyl)nicotinamideHCID 46242011—

反応条件

温度80 °C

反応手順

To the solution of N-[(3-bromopropyl)(oxido)phenyl--sulfanylidene]-5-({3-[(3-methyl-2-furoyl)amino]phenyl}ethynyl)nicotinamide (450 mg, 0.76 mmol) in anhydrous DMF (5 mL) was added dropwise 1-[2-(2-hydroxyethoxy)ethyl]piperazine. The resulting reaction solution was stirred and heated at 80° C. for 30 min. It was then partitioned between saturated aqueous NaHCO3 and EtOAc. The EtOAc layer was separated and washed with brine (1×). The aqueous NaHCO3 layer was extracted with CHCl3 (1×) and the extract was washed with brine (1×). The organic layers were combined and dried over anhydrous sodium sulfate. The organic solution was decanted, concentrated, and wrapped with silica gel. Column chromatography (MeOH-EtOAc from 1:10 to 1:6) rendered the title compound as white foam in amount of 500 mg (96%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07915443B2
出典データセットuspto-grants-2011_03
ORD IDord-a5f58b26d79f44ed82e0b6ec818e5f39
出典メモuspto-grants-2011_03