戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 2187814作成日:2026年10月25日

1-(4-Chlorobenzyl)-4-[[(N-Boc-valyl)amino]methyl]piperidine → 1-(4-Chlorobenzyl)-4-[(valylamino)methyl]piperidine

https://huagongshe.com/reaction/2187814

反応式

関与物質

役割名称HCID仕込み量
反応物1-(4-Chlorobenzyl)-4-[[(N-Boc-valyl)amino]methyl]piperidineHCID 18711802—
溶媒Hydrochloride methanolHCID 21893726—
生成物1-(4-Chlorobenzyl)-4-[(valylamino)methyl]piperidineHCID 5378273197%

反応条件

温度25 °C

反応手順

1-(4-Chlorobenzyl)-4-[{(N-Boc-valyl)amino}methyl]piperidine (1.1 g, 2.51 mmol) was dissolved in 3 M HCl-CH3OH solution (25 mL) and stirred at 25° C. for 1 h. The reaction mixture was concentrated and the resulting salt was dissolved in 3:1 tBuOH—H2O (25 mL). Anion (OH−) exchange resin was added until the solution was slightly basic. Filtration and concentration afforded 1(4-chlorobenzyl)-4-{(valylamino)methyl}piperidine (819 mg, 97%) which required no further purification: RPLC (97%); ESI/MS 338.1 (M++H, C19H28ClN3O).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06410566B1
出典データセットuspto-grants-2002_06
ORD IDord-583a93977f5a457c9fbac88310f01a8f
出典メモuspto-grants-2002_06