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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1418295Generated: November 2, 2026

Propargyl bromide → HCID 101094325, compound

https://huagongshe.com/reaction/1418295

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropargyl bromideHCID 7842—
ReactantPotassium CarbonateHCID 11430—
ReactantAmmonium ChlorideHCID 25517—
ReactantHCID 15390589HCID 15390589—
SolventDiethyl EtherHCID 3283—
SolventAcetonitrileHCID 6342—
ProductHCID 101094325HCID 10109432556.6%

Reaction Steps

An acetonitrile (15 mL) solution of 2-(4-chloro-2-fluoro-5-hydroxyphenyl)-5,6-dihydroimidazo [1,5-a] pyridine-1,3[2H, 7H]-dione (0.82 g, 2.76 mmol), potassium carbonate (0.29 g, 2.07 mmol) and propargylbromide (0.27 mL, 3.04 mmol) was stirred fir 4.5 hours under reflux. A saturated ammonium chloride solution (15 mL) and diethyl ether (15 mL) were added to the resulting mixture, and the organic layer was separated and then the aqueous layer was extracted with diethyl ether (15 mL×2 times). The organic layer combined was washed with a saturated sodium chloride solution (20 mL) and dried over anhydrous magnesium sulfate. After removal of magnesium sulfate by filtration, the filtrate was evaporated to give crude product, which was purified by silica gel column (Wakogel C-200, ethyl acetate/hexane=1/2) to obtain a pale yellow solid of 2-(4-chloro-2-fluoro-5-propargyloxyphenyl)-5,6-dihydroimidazo [1,5-a] pyridine-1,3[2H, 7H]-dione (0.50 g, yield:56.6%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05883049
Source datasetuspto-grants-1999_03
ORD IDord-f12ca30ccb124d96849d02e06867676a
Source noteuspto-grants-1999_03