Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 74226Generated: November 2, 2026

Potassium Carbonate → 2-(2-Cyclopropylaminoanilin-5-yl)benzoxazole

https://huagongshe.com/reaction/74226

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantCyclopropylamineHCID 69828—
Reactant2-(4-Fluoro-3-nitrophenyl)benzoxazoleHCID 21990970—
ReactantHCID 178418361HCID 178418361—
CatalystHCID 178418390HCID 178418390—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product2-(2-Cyclopropylaminoanilin-5-yl)benzoxazoleHCID 6749886146%

Reaction Steps

To a suspension of 2-(4-fluoro-3-nitrophenyl)benzoxazole (see Working Example 15-2) (300 mg, 1.16 mmol) in ethanol (5 mL) was added potassium carbonate (176 mg, 1.28 mmol) and cyclopropylamine (99.3 mg, 1.74 mmol), and this was heated to reflux for 7 hours. After the reaction was complete, this was cooled to room temperature, water was added, and the precipitated crystals were filtered, washed with water and then dried. To a tetrahydrofuran solution (5 mL) of the crystals obtained was added 10% palladium-carbon (50 mg). A hydrogen atmosphere was substituted in the flask, and this was stirred at room temperature for 14 hours. After the reaction was complete, this was filtered through Celite and the filtrate was concentrated. The residue obtained was purified by silica gel column chromatography to yield the title compound (141 mg, 46% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08829035B2
Source datasetuspto-grants-2014_09
ORD IDord-9a9b519d8935419bafb57ea88b38b664
Source noteuspto-grants-2014_09