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HRID 9772作成日:2026年10月24日

1-Pyrrolidineethanamine → 3-bromo-N-[2-(pyrrolidin-1-yl)ethyl]benzamide

https://huagongshe.com/ja/reaction/9772

反応式

関与物質

役割名称HCID仕込み量
反応物1-PyrrolidineethanamineHCID 1344—
反応物TriethylamineHCID 8471—
反応物3-Bromobenzoic acidHCID 11456—
反応物Diethyl cyanophosphonateHCID 76257—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
生成物3-bromo-N-[2-(pyrrolidin-1-yl)ethyl]benzamideHCID 84868585.4%

反応手順

1-(2-Aminoethyl)pyrrolidine (4.34 g), diethyl cyanophosphate (5.57 ml) and triethylamine (10.4 ml) were added to a solution of 3-bromobenzoic acid (5.00 g) in N,N-dimethylformamide (DMF; 60 ml), and the mixture was stirred at room temperature for 16 hours. The reaction mixture was diluted with water and then extracted with diethyl ether. The extract was dried over anhydrous magnesium sulfate, and then the solvent was evaporated under reduced pressure. The residues were crystallized from hexane to give the title compound (6.31 g).

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-20bfb9c6c3334504a550ae3aff9a8c0e
出典メモuspto-grants-2006_08