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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1418307Generated: November 1, 2026

Propargyl bromide → HCID 131721173, compound

https://huagongshe.com/reaction/1418307

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropargyl bromideHCID 7842—
ReactantPotassium CarbonateHCID 11430—
ReactantAmmonium ChlorideHCID 25517—
ReactantHCID 131721169HCID 131721169—
SolventAcetonitrileHCID 6342—
ProductHCID 131721173HCID 13172117365.4%

Reaction Steps

An acetonitrile (10 mL) solution of 2-(2-chloro-4-methyl-5-hydroxyphenyl)-5,6-dihydroimidazo [1,5-a] pyridine-1,3[2H, 7H]-dione (0.34 g, 1.11 mmol), propargylbromide (0.11 mL, 1.22 mmol) and potassium carbonate (0.15 g, 1.11 mmol) was stirred for 30 minutes under reflux. A saturated ammonium chloride solution (20 mL) was added to the resulting mixture and the organic layer was separated. The aqueous layer was extracted with diethyl ether (10 mL×2 times), and the organic layer combined was washed with a saturated sodium chloride solution (40 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=1/4-1/2) to obtain a white solid of 2-(2-chloro-4-methyl-5-propargyloxyphenyl)-5,6-dihydroimidazo [1,5-a] pyridine-1,3[2H, 7H]-dione (0.24 g, yield:63.2%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05883049
Source datasetuspto-grants-1999_03
ORD IDord-66d9cd8184c847ea8e2b029831e7fc4b
Source noteuspto-grants-1999_03