Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1881733Generated: November 2, 2026

Hydrochloric Acid → 1-{2-[4-({[5-chloro-6-(hydroxymethyl)-3-pyridinyl]methyl}amino)-1-piperidinyl]ethyl}-7-fluoro-1,5-naphthyridin-2(1H)-one hydrochloride

https://huagongshe.com/reaction/1881733

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant1-{2-[4-({[5-chloro-6-(hydroxymethyl)-3-pyridinyl]methyl}amino)-1-piperidinyl]ethyl}-7-fluoro-1,5-naphthyridin-2(1H)-oneHCID 46846386—
SolventDichloromethaneHCID 6344—
Product1-{2-[4-({[5-chloro-6-(hydroxymethyl)-3-pyridinyl]methyl}amino)-1-piperidinyl]ethyl}-7-fluoro-1,5-naphthyridin-2(1H)-one hydrochlorideHCID 46846387153.6%

Reaction Steps

To a solution of 1-{2-[4-({[5-chloro-6-(hydroxymethyl)-3-pyridinyl]methyl}amino)-1-piperidinyl]ethyl}-7-fluoro-1,5-naphthyridin-2(1H)-one (Example 1: 163.2 mg, 0.366 mmol) in Dichloromethane (2.5 ml) at 0° C. was added HCl (4M in 1,4-dioxane) (0.092 ml, 0.369 mmol). The reaction mixture was stirred at RT for 30 min, the solvent was evaporated under vacuum and the crude was dispersed in hexane/DCM. The precipitated solid was isolated by filtration under vacuum and washed with DCM and hexane. The obtained solid was dried overnight at 40° C. under vacuum to give 1-{2-[4-({[5-chloro-6-(hydroxymethyl)-3-pyridinyl]methyl}amino)-1-piperidinyl]ethyl}-7-fluoro-1,5-naphthyridin-2(1H)-one hydrochloride (137 mg, 0.281 mmol, 77% yield) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08318940B2
Source datasetuspto-grants-2012_11
ORD IDord-e659c0a880ec4720b75b85905cb4c324
Source noteuspto-grants-2012_11