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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1047158Generated: October 31, 2026

Hydrochloric Acid → (S)-ethyl 6-bromo-4-oxo-1-(piperidin-3-yl)-1,4-dihydro-1,8-naphthyridine-3-carboxylate

https://huagongshe.com/reaction/1047158

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant1,4-DioxaneHCID 31275—
Reactant(S)-ethyl 6-bromo-1-(1-(tert-butoxycarbonyl)piperidin-3-yl)-4-oxo-1,4-dihydro-1,8-naphthyridine-3-carboxylateHCID 68796045—
SolventDichloromethaneHCID 6344—
Product(S)-ethyl 6-bromo-4-oxo-1-(piperidin-3-yl)-1,4-dihydro-1,8-naphthyridine-3-carboxylateHCID 69621276—

Reaction Steps

(S)-ethyl 6-bromo-1-(1-(tert-butoxycarbonyl)piperidin-3-yl)-4-oxo-1,4-dihydro-1,8-naphthyridine-3-carboxylate (Intermediate 30, 10.847 g, 22.58 mmol) was taken up in dichloromethane (10 mL) and added HCl 4M in Dioxane (113 mL, 451.63 mmol) while stirring at RT for 1 h. The solvent was removed in vacuo and the residue was triturated with DCM, ether and EtOAc to give the desired product as a yellow solid. (S)-ethyl 6-bromo-4-oxo-1-(piperidin-3-yl)-1,4-dihydro-1,8-naphthyridine-3-carboxylate (8.50 g, 90%) was recovered as the HCl salt. MS (ES)(M+H)+: 381 for C16H18BrN3O3.[HCl].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08569484B2
Source datasetuspto-grants-2013_10
ORD IDord-614eafb8d6ef44d4b2873e968ba61b9d
Source noteuspto-grants-2013_10