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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1620059Generated: November 2, 2026

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

https://huagongshe.com/reaction/1620059

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 numberUS08772320B2
Source datasetuspto-grants-2014_07
ORD IDord-ff9b61a89a234b09a64cc52ad073995a
Source noteuspto-grants-2014_07