Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 228950Generated: October 25, 2026

Sulfuric Acid → 2-[4-(5,6-Dimethyl-[2,3']bipyridin-3-yloxy)-6-methoxy-quinolin-7-yloxymethyl]-propane-1,3-diol

https://huagongshe.com/reaction/228950

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantTriphenylphosphineHCID 11776—
ReactantSodium HydroxideHCID 14798—
Reactant(2,2-Dimethyl-1,3-dioxan-5-yl)methanolHCID 3584869—
ReactantDiethyl azodicarboxylateHCID 5462977—
Reactant4-(5,6-Dimethyl-[2,3']bipyridin-3-yloxy)-6-methoxy-quinolin-7-olHCID 136131618—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product2-[4-(5,6-Dimethyl-[2,3']bipyridin-3-yloxy)-6-methoxy-quinolin-7-yloxymethyl]-propane-1,3-diolHCID 5775647256%

Reaction Steps

4-(5,6-Dimethyl-[2,3′]bipyridin-3-yloxy)-6-methoxy-quinolin-7-ol (compound 345) (80 mg) was dissolved in tetrahydrofuran (2 ml) to prepare a solution. Triphenylphosphine (112 mg), (2,2-dimethyl-[1,3]dioxan-5-yl)-methanol (38 mg), and diethylazodicarboxylate (0.078 ml) were added to the solution, and the mixture was stirred at room temperature for 6 hr. Further, 1 N sulfuric acid (4 ml) was added thereto, and the mixture was stirred at room temperature overnight. The reaction solution was brought to 0° C., was stirred, and was made alkaline by the addition of a 10% aqueous sodium hydroxide solution. Water was added thereto, and the mixture was extracted with ethyl acetate. The ethyl acetate layer was then washed with saturated brine 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 chloroform-methanol to give the title compound (54 mg, yield 56%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07560558B2
Source datasetuspto-grants-2009_07
ORD IDord-5ace09aed363468f99c703a7c94c714f
Source noteuspto-grants-2009_07