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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1513037Generated: November 4, 2026

Hydrochloric Acid → 3-[2-Chloro-5-(3,4-dihydroquinolin-1(2H)-ylsulfonyl)phenyl]-1,3-dihydro-2H-imidazo-[4,5-b]pyridin-2-one

https://huagongshe.com/reaction/1513037

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDimethylformamideHCID 6228—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Chloronicotinic acidHCID 76258—
Reactant1-(3-Amino-4-chlorobenzenesulfonyl)-1,2,3,4-tetrahydroquinolineHCID 23120041—
CatalystCopperHCID 23978—
Product3-[2-Chloro-5-(3,4-dihydroquinolin-1(2H)-ylsulfonyl)phenyl]-1,3-dihydro-2H-imidazo-[4,5-b]pyridin-2-oneHCID 59310075—

Reaction Conditions

Temperature100 °C

Reaction Steps

To a mixture of 2-chloronicotinic acid (0.13 g) and 2-chloro-5-(3,4-dihydroquinolin-1(2H)-ylsulfonyl)aniline (0.3 g) in N,N-dimethylformamide (2 mL) were added copper powder (6 mg) and potassium carbonate (0.13 g), and the mixture was heated at reflux for 8 hours. The reaction mixture was poured into 1 mol/L hydrochloric acid, and the resulting mixture was extracted with ethyl acetate. The extract was washed with water and brine, and dried over anhydrous magnesium sulfate. The solvent was removed under reduced pressure, and the residue was dissolved in 1,4-dioxane (10 mL) To the solution were added triethylamine (0.42 mL) and diphenylphosphoryl azide (0.26 mL), and the mixture was stirred at 100° C. for 3 hours. The reaction mixture was poured into 1 mol/L hydrochloric acid, and the resulting mixture was extracted with ethyl acetate. The extract was washed with water and brine, and dried over anhydrous magnesium sulfate. The solvent was removed under reduced pressure, and the residue was purified by column chromatography on silica gel (eluent: n-hexane/ethyl acetate=1/1−1/2) to give the title compound (48 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08217069B2
Source datasetuspto-grants-2012_07
ORD IDord-632a8fb5b9614275a1cae57a099b1fa6
Source noteuspto-grants-2012_07