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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2175614Generated: November 2, 2026

2,3-Dichloro-5,6-dicyano-1,4-benzoquinone → 1,6-Naphthyridin-5(6H)-one, 3-(trifluoromethyl)-

https://huagongshe.com/reaction/2175614

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,3-Dichloro-5,6-dicyano-1,4-benzoquinoneHCID 6775—
Reactant3-(Trifluoromethyl)-7,8-dihydro-1,6-naphthyridin-5(6H)-oneHCID 58562777—
Solvent1,4-DioxaneHCID 31275—
Product1,6-Naphthyridin-5(6H)-one, 3-(trifluoromethyl)-HCID 58562733—

Reaction Conditions

Temperature100 °C

Reaction Steps

Into a 100 mL round-bottom flask, was placed a solution of 3-(trifluoromethyl)-7,8-dihydro-1,6-naphthyridin-5(6H)-one (as prepared in the previous step, 1.7 g, 7.87 mmol, 1.00 equiv) in dioxane (20 mL) and 2,3-Dichloro-5,6-dicyano-1,4-benzoquinone (2.68 g, 11.81 mmol, 1.50 equiv). The reaction mixture was stirred for 6 h at 100° C. in an oil bath. The resulting mixture was concentrated under vacuum and the residue was dissolved in 20 mL of sodium bicarbonate. The resulting solution was extracted with 3×100 mL of dichloromethane, and the combined organic layers dried over sodium sulfate and concentrated under vacuum. The residue was purified by chromatography over a silica gel column with ethyl acetate/petroleum ether (1:10-1:2). The title compound was obtained as a light yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09062048B2
Source datasetuspto-grants-2015_06
ORD IDord-4539f8d9cde5419c8fee607631bbb780
Source noteuspto-grants-2015_06