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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 523077Generated: October 30, 2026

Methyl iodide → 7-Bromo-2-methyl-1,6-naphthyridine

https://huagongshe.com/reaction/523077

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium methanethiolateHCID 4378561—
Reactant(E)-4-(4-Amino-6-bromopyridin-3-yl)but-3-en-2-oneHCID 89995621—
SolventEthanolHCID 702—
Product7-Bromo-2-methyl-1,6-naphthyridineHCID 8999561990%

Reaction Steps

(E)-4-(4-Amino-6-bromopyridin-3-yl)but-3-en-2-one (Preparation 66, 331 mg 1.37 mmol) and sodium thiomethoxide (97.5 mg 1.39 mmol) were stirred in ethanol (2.9 mL) at 20° C. for 50 minutes. Iodomethane (86 uL, 1.38 mmole) was added and the reaction stirred for another 45 minutes. The reaction was concentrated in vacuo and diluted with ethyl acetate (30 mL) and washed with water (10 mL). The aqueous was back extracted with ethyl acetate (5 mL) and the combined organic layers were washed with brine, dried over sodium sulfate and concentrated in vacuo to afford the title compound (275 mg, 89%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09334286B2
Source datasetuspto-grants-2016_05
ORD IDord-77f27829e73446deb99cc615115187ac
Source noteuspto-grants-2016_05