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HRID 534782作成日:2026年10月27日

Diisopropylethylamine → 1,1-Dimethylethyl (2S)-4-[(2-chloro-4-nitrophenyl)methyl]-2-methyl-1-piperazinecarboxylate

https://huagongshe.com/reaction/534782

反応式

関与物質

役割名称HCID仕込み量
反応物DiisopropylethylamineHCID 81531—
反応物1-(Bromomethyl)-2-chloro-4-nitrobenzeneHCID 3016368—
反応物(S)-tert-butyl 2-methylpiperazine-1-carboxylate hydrochlorideHCID 45072182—
溶媒DimethylformamideHCID 6228—
溶媒DichloromethaneHCID 6344—
生成物1,1-Dimethylethyl (2S)-4-[(2-chloro-4-nitrophenyl)methyl]-2-methyl-1-piperazinecarboxylateHCID 5926212834.5%

反応手順

A mixture of crude 1-(bromomethyl)-2-chloro-4-nitrobenzene (D102) (0.391 g), 1,1-dimethylethyl (2S)-2-methyl-1-piperazinecarboxylate hydrochloride (0.407 g, 1.72 mmol) and Hunig's base (0.625 mL, 3.59 mmol) in dry DMF (3 mL) was stirred at room temperature for 10 minutes. The reaction mixture was concentrated to give an orange oil which was dissolved in DCM and washed with water (×2) and brine, then dried and concentrated to give an orange oil. Purification by column chromatography eluting with 0-30% EtOAc/pentane gave the title compound as a yellow oil (0.199 g). δH (CDCl3, 400 MHz) 8.24 (1H, d), 8.12 (1H, dd), 7.77 (1H, d), 4.24 (1H, br.s), 3.85 (1H, d), 3.63 (2H, s), 3.14 (1H, td), 2.76 (1H, m), 2.59 (1H, m), 2.33 (1H, dd), 2.18 (1H, m), 1.47 (9H, s), 1.28 (3H, d). MS (ES): MH+ 370/372,

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08853218B2
出典データセットuspto-grants-2014_10
ORD IDord-92ef30901bb549da81580cf8c3595c75
出典メモuspto-grants-2014_10