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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 133589Generated: October 25, 2026

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

https://huagongshe.com/reaction/133589

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 a 3 M HCl-methanol solution (25 mL) and stirred at 25° C. for 1 hour. The resulting reaction mixture was concentrated, and the obtained salt was dissolved in tBuOH/H2O=3:1 (25 mL). An anion (OH−) exchange resin was added until the solution became slightly basic. The obtained mixture was filtered and concentrated to provide 1-(4-chlorobenzyl)-4-[(valylamino)methyl]piperidine (819 mg, 97%). Further purification was not required for the resulting compound. ESI/MS m/e 338.1 (M++H, C18H28ClN3O).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07390830B1
Source datasetuspto-grants-2008_06
ORD IDord-65c0d8cbe6fd471eba161484b6414d78
Source noteuspto-grants-2008_06