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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1986677Generated: November 3, 2026

2,3-Dichloro-5,6-dicyano-1,4-benzoquinone → 7-Fluoroquinolin-2(1H)-one

https://huagongshe.com/reaction/1986677

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,3-Dichloro-5,6-dicyano-1,4-benzoquinoneHCID 6775—
ReactantCarbostyril, 3,4-dihydro-7-fluoro-HCID 138300—
Solvent1,4-DioxaneHCID 31275—
Product7-Fluoroquinolin-2(1H)-oneHCID 1906757518.9%

Reaction Steps

DDQ (0.42 g, 1.9 mmol) was added to a solution of 7-fluoro-3,4-dihydro-1H-quinolin-2-one (0.20 g 1.2 mmol) in dioxane (25 mL) and the resulting mixture was refluxed under an Argon atmosphere for 16 h. The mixture was concentrated under reduced pressure and sat aqueous Na2CO3 solution (25 mL) was added, and this was extracted with an organic mixture (MeOH/CH2Cl2 1:10, 3×50 mL). The combined organic phase was dried (Na2SO4), filtered, concentrated under reduced pressure and purified by combi flash LC (SiO2; CH2Cl2/MeOH 10:1) to give the title compound (0.037 g, 18%). 1H NMR (DMSO-D6) δ 11.8 (s, 1H), 7.88 (d, J=9.6 Hz, 1H), 7.74-7.65 (m, 1H), 7.05-6.95 (m, 2H), 6.43, (d, J=9.6 Hz); 13C NMR (CDMSO-D6) δ 163.0 (d, J=247 Hz), 161.9, 140.4 (d, J=13 Hz), 130.4 (d, J=11 Hz), 120.9, 116.1, 109.8 (d, J=23), 101.0 (d, J=25 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07550459B2
Source datasetuspto-grants-2009_06
ORD IDord-95d5f85c9d41441d8406e355bb6dc346
Source noteuspto-grants-2009_06