戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 711379作成日:2026年10月26日

1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → Tert-butyl 4-(2-(7-bromoquinoxalin-2-yl)hydrazinecarbonyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/711379

反応式

関与物質

役割名称HCID仕込み量
反応物1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
反応物1-HydroxybenzotriazoleHCID 75771—
反応物1-(tert-Butoxycarbonyl)-4-piperidinecarboxylic acidHCID 392871—
反応物7-Bromo-2-hydrazinylquinoxalineHCID 5200265—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
生成物Tert-butyl 4-(2-(7-bromoquinoxalin-2-yl)hydrazinecarbonyl)piperidine-1-carboxylateHCID 6680341062%

反応手順

A mixture of 7-bromo-2-hydrazinylquinoxaline (3 g, 12.55 mmol), 1-(tert-butoxycarbonyl)piperidine-4-carboxylic acid (3.16 g, 13.81 mmol), EDCI (2.89 g, 15.06 mmol), HOBt (2.03 g, 15.06 mmol), and TEA (1.9 g, 18.83 mmol) in DMF (100 mL) was stirred at r.t. overnight. The mixture was diluted with water (10 mL), and extracted with EtOAc (3×100 mL). The combined layers were dried over Na2SO4, and concentrated in vacuo to afford tert-butyl 4-(2-(7-bromoquinoxalin-2-yl)hydrazinecarbonyl)piperidine-1-carboxylate as pale yellow solid (3.5 g, yield 62%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09181264B2
出典データセットuspto-grants-2015_11
ORD IDord-6daeb1f3657544e390363fbe587464e1
出典メモuspto-grants-2015_11