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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 228861Generated: November 1, 2026

Water → 6,7-Dimethoxy-4-(7-phenyl-benzothiazol-6-yloxy)-quinoline

https://huagongshe.com/reaction/228861

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
ReactantPhenylboronic AcidHCID 66827—
Reactant4-(7-Iodo-benzothiazol-6-yloxy)-6,7-dimethoxy-quinolineHCID 23078332—
SolventDimethylformamideHCID 6228—
Product6,7-Dimethoxy-4-(7-phenyl-benzothiazol-6-yloxy)-quinolineHCID 2307829398%

Reaction Conditions

Temperature80 °C

Reaction Steps

4-(7-Iodo-benzothiazol-6-yloxy)-6,7-dimethoxy-quinoline (compound 294) (40 mg), phenylboronic acid (40 mg), and tetrakistriphenylphosphine palladium (20 mg) were dissolved in N,N-dimethylformamide (5 ml) to prepare a solution. A 2 M aqueous potassium carbonate solution (0.3 ml) was added to the reaction system, and the mixture was stirred at 80° C. for 20 min. Water was added to the reaction solution, and the mixture was extracted with ethyl acetate. The ethyl acetate layer was then washed with water and was dried over anhydrous sodium sulfate. The solvent was removed by distillation under the reduced pressure, and the residue was purified by thin layer chromatography using acetone-chloroform to give the title compound (35 mg, yield 98%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07560558B2
Source datasetuspto-grants-2009_07
ORD IDord-83bd29e4a25d41dba88e9878e03c2759
Source noteuspto-grants-2009_07