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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1277422Generated: November 1, 2026

2,3-Dichloro-5,6-dicyano-1,4-benzoquinone → 6-[3-(1-Cyclohexyl-1H-tetrazol-5-yl) propoxy]-2(1H)-quinolinone

https://huagongshe.com/reaction/1277422

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,3-Dichloro-5,6-dicyano-1,4-benzoquinoneHCID 6775—
Reactant1,4-DioxaneHCID 31275—
Reactant6-[3-(1-Cyclohexyl-1H-tetrazol-5-yl)propoxy]-3,4-dihydroquinolin-2(1H)-oneHCID 12941267—
SolventChloroformHCID 6212—
Product6-[3-(1-Cyclohexyl-1H-tetrazol-5-yl) propoxy]-2(1H)-quinolinoneHCID 13021094—

Reaction Steps

3.2 Grams of 6-[3-(1-cyclohexyltetrazol-5-yl)propoxy]-3,4-dihydrocarbostyril and 3.4 g of 90% DDQ are added to 100 ml of dioxane and this mixture is refluxed for9.5 hours and then cooled. After the reaction is completed, the solvent is distilled off and the residue obtained is dissolved in chloroform and the organic layer is washed with aqueous saturated NaHCO3 solution, and with water then dried with Na2SO4 and treated with an activatedcharcoal. After the solvent is removed by distillation, the resultant residue is refined by silica gel column chromatography [silica gel: Wakogel C-200; eluent:chloroform:methanol=10:1 (V/V)] and the crude crystals are recrystallized from chloroform to obtain 1.1 g of 6-[3-(1-cyclohexyltetrazol-5-yl)propoxy]carbostyril in the form of colorless needle-like crystals. Melting point: 211°-212° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04277479
Source datasetuspto-grants-1981_07
ORD IDord-8b1955972c244624baf6b2bf57905678
Source noteuspto-grants-1981_07