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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2406707Generated: October 31, 2026

Dichloromethane → 5-(5-Bromopyridin-3-YL)oxazole

https://huagongshe.com/reaction/2406707

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
Reactant5-Bromo-3-pyridinecarboxaldehydeHCID 2784734—
ReactantToluenesulfonylmethyl isocyanideHCID 53627694—
SolventWaterHCID 962—
Product5-(5-Bromopyridin-3-YL)oxazoleHCID 6705592079.3%

Reaction Steps

Toluenesulfonylmethylisocyanide (126 mg) and 1,8-diazabicyclo[5.4.0]undec-7-ene (122 mg) were added to a dichloromethane (4 ml) solution containing 5-bromo-3-pyridinecarboxaldehyde (100 mg) at room temperature, followed by stirring for 5 hours. Water was added to the reaction solution, followed by extraction with ethyl acetate. The resultant was washed with saturated saline and dried over anhydrous sodium sulfate. Subsequently, the solvent was distilled away under reduced pressure, the obtained residue was purified by silica gel chromatography (n-hexane:ethyl acetate=4:1 to 5:2), and a white solid of 5-(5-bromopyridin-3-yl)oxazole (96 mg) was thus obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08809371B2
Source datasetuspto-grants-2014_08
ORD IDord-11789915ec3742aa93885f967d20ee2b
Source noteuspto-grants-2014_08