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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2120767Generated: October 31, 2026

Methyl iodide → 6-bromo-N-(4-chlorobenzyl)-1,7-dimethyl-4-oxo-1,4-dihydro[1,8]naphthyridine-3-carboxamide

https://huagongshe.com/reaction/2120767

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 178432387HCID 178432387—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product6-bromo-N-(4-chlorobenzyl)-1,7-dimethyl-4-oxo-1,4-dihydro[1,8]naphthyridine-3-carboxamideHCID 1209331386.8%

Reaction Steps

To a solution of 6-bromo-N-(4-chlorobenzyl)4-hydroxy-7-methyl[1,8]naphthyridine-3-carboxamide (0.400 g, 0.98 mmol) and potassium carbonate (0.54 g, 3.92 mmol) in 5 mL DMF at room temperature is added dropwise methyl iodide (0.167 g, 1.18 mmol). The mixture is stirred at room temperature for 30 min then diluted with water. The resulting solid is filtered, washed with water and dried. The crude product is triturated with EtOAc/hexanes to yield 0.358 g (85%) of the desired product as a white solid. Physical characteristics are as follows: m.p. 266-268° C.; 1H NMR (CDCl3) δ10.18, 8.92, 8.83, 7.30, 4.65, 4.03, 2.82; Anal. Calcd for C18H15BrClN3O2: C, 51.39; H, 3.59; N, 9.99; Found: C, 51.02; H, 3.57; N, 9.94.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06693114B2
Source datasetuspto-grants-2004_02
ORD IDord-169c04b34bdb47a2a2ba9f1bb11cc50a
Source noteuspto-grants-2004_02