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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1874405Generated: October 31, 2026

Ethyl isocyanate → HCID 57749114, compound

https://huagongshe.com/reaction/1874405

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl isocyanateHCID 8022—
ReactantHCID 57749303HCID 57749303—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 57749114HCID 5774911425.3%

Reaction Steps

To a solution of N-{5-[(2-aminoimidazo[1,2-a]pyridin-6-yl) oxy]-2-fluorophenyl}-1,3-dimethyl-1H-pyrazole-5-carboxamide (70.0 mg, 0.184 mmol) in tetrahydrofuran (3 mL) was added ethyl isocyanate (17.5 μL, 0.221 mmol), and the mixture was stirred at room temperature for 15 hr. The reaction mixture was diluted with water and extracted with ethyl acetate. The organic layer was washed with water and saturated brine, dried over anhydrous magnesium sulfate and filtrated. The filtrate was concentrated under reduced pressure, and the residue was purified by column chromatography (NH silica gel, ethyl acetate) and recrystallized from ethyl acetate-ethanol to give the title compound (21.0 mg, 25%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08304557B2
Source datasetuspto-grants-2012_11
ORD IDord-d62fd1dd37054d1abc84c8a5dfedff5e
Source noteuspto-grants-2012_11