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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 403129Generated: October 28, 2026

N-(2-tert-butoxybenzyl)-3-(4-phenylpiperidin-1-yl)-N-(pyridin-2-ylmethyl)propan-1-amine → 2-(((3-(4-Phenylpiperidin-1-yl)propyl)(pyridin-2-ylmethyl)amino)methyl)phenol

https://huagongshe.com/reaction/403129

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(2-tert-butoxybenzyl)-3-(4-phenylpiperidin-1-yl)-N-(pyridin-2-ylmethyl)propan-1-amineHCID 70896369—
SolventHydrochloric AcidHCID 313—
SolventEthyl AcetateHCID 8857—
Product2-(((3-(4-Phenylpiperidin-1-yl)propyl)(pyridin-2-ylmethyl)amino)methyl)phenolHCID 4985009692%

Reaction Steps

Compound 20 (0.15 g, 0.31 mmol) was dissolved in 25 mL EtOAc saturated with HCl and stirred for 3 hr. The solvent was evaporated to dryness. The residue was purified on a silica gel TLC plate that was developed in 8% methanolic NH3 (7 M NH3 in methanol/92% CH2Cl2. The product was obtained as white solid (92%). 1H NMR (CDCl3) δ 8.589 (dd, 1H, Ar), 7.675 (ddd, 1H, Ar), 7.332 (d, 1H, Ar), 7.289 (ddd, 3H, Ar), 7.189 (m, 5H, Ar), 7.009 (dd, 1H, Ar), 6.854 (dd, 1H, Ar), 6.780 (ddd, 1H, Ar), 3.843 (s, 2H, —CH2—), 3.798, (s, 2H, —CH2—), 2.974 (d, 2H, —CH2—), 2.633 (t, 2H, —CH2—), 2.458 (m, 1H, —CH—), 2.333 (m, 2H, —CH2—), 2.000 (m, 2H, —CH2—), 1.782 (m (br), 6H). Mass Spec.=416.27 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08747810B2
Source datasetuspto-grants-2014_06
ORD IDord-5253f0e77a924818a0b7397643b10914
Source noteuspto-grants-2014_06