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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 1-{2-[4-({[5-chloro-6-(hydroxymethyl)-3-pyridinyl]methyl}amino)-1-piperidinyl]ethyl}-7-fluoro-1,5-naphthyridin-2(1H)-one | HCID 46846386 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-{2-[4-({[5-chloro-6-(hydroxymethyl)-3-pyridinyl]methyl}amino)-1-piperidinyl]ethyl}-7-fluoro-1,5-naphthyridin-2(1H)-one hydrochloride | HCID 46846387 | 153.6% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08318940B2 |
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| Source dataset | uspto-grants-2012_11 |
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| ORD ID | ord-e659c0a880ec4720b75b85905cb4c324 |
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| Source note | uspto-grants-2012_11 |
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