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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1070656Generated: October 30, 2026

Water → Ethyl 6-Chloro-1-methyl-4-oxo-1,4-dihydro[1,5]naphthyridine-3-carboxylate

https://huagongshe.com/reaction/1070656

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
ReactantEthyl 6-chloro-4-hydroxy[1,5]naphthyridine-3-carboxylateHCID 178469542—
SolventDimethylformamideHCID 6228—
ProductEthyl 6-Chloro-1-methyl-4-oxo-1,4-dihydro[1,5]naphthyridine-3-carboxylateHCID 2239713665%

Reaction Steps

A mixture of ethyl 6-chloro-4-hydroxy[1,5]naphthyridine-3-carboxylate (Preparation 58, 694 mg), potassium carbonate (588 mg), and iodomethane (264 μL) in DMF (15 mL) is stirred at room temperature for 5 hours. The mixture is poured into water (50 mL), and the solution is extracted with CH2Cl2 (3×50 mL). The organic layers are dried (MgSO4) and concentrated. Trituration with ether (50 mL) affords 473 mg (65%) of the title compound as an off-white solid. Physical Characteristics. 1H NMR (DMSO-d6) δ8.70, 8.31, 7.90, 4.24, 3.92, 1.29; HRMS (FAB) m/z 267.0535 (C12H11ClN2O3+H). Anal. Found: C, 54.14; H, 4.24; N, 10.58.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06903097B2
Source datasetuspto-grants-2005_06
ORD IDord-2f89db75b04f478a8ef350bb3765390a
Source noteuspto-grants-2005_06