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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-(4-Chlorobenzyl)-4-[[(N-Boc-valyl)amino]methyl]piperidine | HCID 18711802 | — |
| Solvent | Hydrochloride methanol | HCID 21893726 | — |
| Product | 1-(4-Chlorobenzyl)-4-[(valylamino)methyl]piperidine | HCID 53782731 | 97% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07390830B1 |
|---|
| Source dataset | uspto-grants-2008_06 |
|---|
| ORD ID | ord-65c0d8cbe6fd471eba161484b6414d78 |
|---|
| Source note | uspto-grants-2008_06 |
|---|