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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1085114Generated: November 1, 2026

1,8-Diazabicyclo(5.4.0)undec-7-ene → 6-[3-(1H-1,2,4-triazol-1-yl)propylthio]-3,4-dihydrocarbostyril

https://huagongshe.com/reaction/1085114

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
Reactant6-Mercapto-3,4-dihydroquinolin-2(1H)-oneHCID 13109832—
Reactant1-(3-bromopropyl)-1H-1,2,4-triazoleHCID 18669172—
SolventIsopropanolHCID 3776—
Product6-[3-(1H-1,2,4-triazol-1-yl)propylthio]-3,4-dihydrocarbostyrilHCID 14207214—

Reaction Steps

2.4 Grams (13.4 mM) of 6-mercapto-3,4-dihydrocarbostyril, 3,3 g (17.4 mM) of 1-(3-bromopropyl)-1,2,4-triazol, and 2.6 ml (17.4 mM) of DBU were added to 60 ml of isopropanol, and the whole mixture was refluxed by heating for 2 hours. After the reaction was completed, the reaction mixture was concentrated, the resulting residue was extracted with chloroform. The chloroform extract was washed with water, an aqueous solution saturated with sodium hydrogen carbonate, and water in this order, then dried with anhydrous sodium sulfate. The dried extract was concentrated by removing the solvent by evaporation, the residue was purified by means of a silica gel column chromatography (eluent: dichloromethane: methanol=20:1), and recrystallized from ethanol-n-hexane to yield 2.5 g of 6-[3-(1H-1,2,4-triazol-1-yl)propylthio]-3,4-dihydrocarbostyril. Colorless needle-like crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05008274
Source datasetuspto-grants-1991_04
ORD IDord-ee98519484cb469e8ead7f05cb6c9b31
Source noteuspto-grants-1991_04