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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 279298Generated: October 25, 2026

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

https://huagongshe.com/reaction/279298

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(4-Chlorobenzyl)-4-[[(N-Boc-valyl)amino]methyl]piperidineHCID 18711802—
SolventHydrochloride methanolHCID 21893726—
Product1-(4-Chlorobenzyl)-4-[(valylamino)methyl]piperidineHCID 5378273197%

Reaction Conditions

Temperature25 °C

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06362177B1
Source datasetuspto-grants-2002_03
ORD IDord-2b1911c084ff48d791174914f5235026
Source noteuspto-grants-2002_03