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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1280997생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/1280997

반응식

참여 물질

역할이름HCID투입량
반응물1-(4-Chlorobenzyl)-4-[[(N-Boc-valyl)amino]methyl]piperidineHCID 18711802—
용매Hydrochloride methanolHCID 21893726—
생성물1-(4-Chlorobenzyl)-4-[(valylamino)methyl]piperidineHCID 5378273197%

반응 조건

온도25 °C

반응 단계

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, C18H28ClN3O).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06451842B1
출처 데이터셋uspto-grants-2002_09
ORD IDord-d2acc9c6529f4fe9bee3a70efcf91315
출처 메모uspto-grants-2002_09