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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1047159Generated: October 25, 2026

Potassium Carbonate → (S)-ethyl 6-bromo-1-(1-(2-morpholinoethyl)piperidin-3-yl)-4-oxo-1,4-dihydro-1,8-naphthyridine-3-carboxylate

https://huagongshe.com/reaction/1047159

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant4-(2-Bromoethyl)morpholine hydrochlorideHCID 12955540—
Reactant(S)-ethyl 6-bromo-4-oxo-1-(piperidin-3-yl)-1,4-dihydro-1,8-naphthyridine-3-carboxylate hydrochlorideHCID 86665046—
SolventAcetonitrileHCID 6342—
Product(S)-ethyl 6-bromo-1-(1-(2-morpholinoethyl)piperidin-3-yl)-4-oxo-1,4-dihydro-1,8-naphthyridine-3-carboxylateHCID 69621275—

Reaction Conditions

Temperature120 °C

Reaction Steps

(S)-ethyl 6-bromo-4-oxo-1-(piperidin-3-yl)-1,4-dihydro-1,8-naphthyridine-3-carboxylate hydrochloride Intermediate 33, 0.400 g, 0.96 mmol) and K2CO3 (0.663 g, 4.80 mmol) were taken up in acetonitrile (3 mL) and 4-(2-bromoethyl)morpholine hydrochloride (0.221 g, 0.96 mmol) added. The reaction mixture was heated to 120° C. in the microwave for 30 min. The reaction mixture was cooled to room temperature and filtered, and the inorganics were washed with EtOAc two times. The solvent was removed in vacuo. (S)-ethyl 6-bromo-1-(1-(2-morpholinoethyl)piperidin-3-yl)-4-oxo-1,4-dihydro-1,8-naphthyridine-3-carboxylate (0.420 g, 89%) was recovered as a tan solid and will be carried on without further purification. MS (ES)(M+H)+: 494 for C22H29BrN4O4.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08569484B2
Source datasetuspto-grants-2013_10
ORD IDord-a05205c87013454993e89832e700d999
Source noteuspto-grants-2013_10