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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1297638Generated: October 30, 2026

Dimethylformamide → 6-Formyl-4-methoxy-3-(5-methyl-oxazol-2-yl)-quinoline

https://huagongshe.com/reaction/1297638

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantCID 76231HCID 76231—
ReactantDiphenylpropyl phosphineHCID 53436545—
Reactant6-Iodo-4-methoxy-3-(5-methyl-oxazol-2-yl)-quinolineHCID 58585778—
Catalystpalladium(II) acetateHCID 167845—
Product6-Formyl-4-methoxy-3-(5-methyl-oxazol-2-yl)-quinolineHCID 5858586140%

Reaction Steps

A mixture of 6-iodo-4-methoxy-3-(5-methyl-oxazol-2-yl)-quinoline (example 16c) (492 mg, 1.34 mmol), trethylamine (0.46 mL, 3.35 mmol), diphenylpropylphosphine (dpp, 31 uL, 0.13 mmol) and palladium(II) acetate (31 mg, 0.13 mmol) in dry N,N-dimethylformamide (20 mL) in pressure tube was stirred under carbon monoxide at 75 psi at room temperature for 10 min. After addition of trihexylsilane (1.01 mL, 2.68 mmol), the mixture was then stirred under carbon monoxide at 75 psi at 80° C. for 5 h. The reaction was allowed to cool to 25° C. and then extracted with ethyl acetate (2×100 mL). The combined organic layers were successively washed with a saturated aqueous sodium bicarbonate solution (3×50 mL) and water (3×50 mL), dried over sodium sulfate, filtered, and concentrated in vacuo. Flash chromatography (Merck Silica gel 60, 70-230 mesh, 0%-50% ethyl acetate in hexanes in 30 min) afforded 6-formyl-4-methoxy-3-(5-methyl-oxazol-2-yl)-quinoline (144 mg, 40%) as a white solid. LC-MS m/e 269 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07250515B2
Source datasetuspto-grants-2007_07
ORD IDord-7050115c10484c39b2157872993d24ae
Source noteuspto-grants-2007_07