HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1281022Generated: October 26, 2026
Acetic Acid → 4-[{N-(2-amino-5-chlorobenzoyl)glycyl}aminomethyl]-1-(4-ethoxybenzyl)piperidine
https://huagongshe.com/reaction/1281022
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | 4-Ethoxybenzaldehyde | HCID 24834 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | 4-[{N-(2-amino5-chlorobenzoyl)glycyl}aminomethyl]piperidine | HCID 18426216 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 4-[{N-(2-amino-5-chlorobenzoyl)glycyl}aminomethyl]-1-(4-ethoxybenzyl)piperidine | HCID 18426129 | — |
Reaction Steps
Sodium cyanoborohydride (140 mmol) in methanol (0.4 mL) was added to a mixture of 4-[{N -(2-amino-5-chlorobenzoyl)glycyl}aminomethyl]piperidine (0.10 mmol), 4-ethoxybenzaldehyde (0.10 mmol), acetic acid (0.050 mL), and methanol (1.6 mL). The reaction mixture was stirred at 60° C. for 14 h. The reaction mixture was loaded onto Varian™ SCX column and washed with CH3OH (20 mL). Product was eluted using 2 N NH3 in CH3OH (6 mL) and concentrated. Preparative TLC (SiO2, AcOEt/CH3OH 5:1) afforded 4-[{N-(2-amino-5-chlorobenzoyl)glycyl}aminomethyl]-1-(4-ethoxybenzyl)piperidine (Compound No. 1429) and 1-(4-ethoxybenzyl)-4-[{N-(2-(4-ethoxybenzyl)amino-5-chlorobenzoyl)glycyl}aminomethyl]piperidine (Compound No. 1433).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06451842B1 |
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| Source dataset | uspto-grants-2002_09 |
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| ORD ID | ord-31fdb762b3ff45edad25234423c1e24a |
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| Source note | uspto-grants-2002_09 |
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