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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2083930Generated: November 1, 2026

2-Chloro-N-(4-methoxyphenyl)-3-pyridinecarboxamide → N-(4-Methoxyphenyl)-2-[1-(4-pyridyl)piperidin-4-ylmethyl]aminopyridine-3-carboxamide

https://huagongshe.com/reaction/2083930

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloro-N-(4-methoxyphenyl)-3-pyridinecarboxamideHCID 840301—
Reactant[1-(Pyridin-4-yl)piperidin-4-yl]methanamineHCID 10607746—
SolventEthanolHCID 702—
ProductN-(4-Methoxyphenyl)-2-[1-(4-pyridyl)piperidin-4-ylmethyl]aminopyridine-3-carboxamideHCID 984487024%

Reaction Steps

A pressure tube (Aldrich) was charged with 2-chloro-N-(4-methoxyphenyl)pyridine-3-carboxamide (139 mg, 0.524 mmol), 1-(4-pyridyl)piperidine-4-methylamine (100 mg, 0.524 mmol), triethylanine (0.22 mL), and ethanol (3 mL). The mixture was placed in a 110° C. bath for 5 days. The mixture was concentrated and the residue purified by RPHPLC, yielding 52 mg (24%) of the title compound as a hydrochloride salt.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06716839B2
Source datasetuspto-grants-2004_04
ORD IDord-b452d6c4f5684e5590dd84427971d464
Source noteuspto-grants-2004_04