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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1418312Generated: November 1, 2026

Propargyl bromide → HCID 131721179, compound

https://huagongshe.com/reaction/1418312

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropargyl bromideHCID 7842—
ReactantPotassium CarbonateHCID 11430—
ReactantAmmonium ChlorideHCID 25517—
ReactantHCID 131721175HCID 131721175—
SolventAcetonitrileHCID 6342—
ProductHCID 131721179HCID 13172117973.2%

Reaction Steps

An acetonitrile (10 mL) solution of 2-(2,4-dichloro-5-hydroxyphenyl)-5,6-dihydroimidazo [1,5-a] pyridine-1,3[2H, 7H]-dione (0.50 g, 1.61 mmol), propargylbromide (0.16 mL, 1.77 mmol) and potassium carbonate (0.22 g, 1.61 mmol) was stirred for 3 hours under reflux. A saturated ammonium chloride solution (20 mL) was added to the resulting mixture 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=1/2) to obtain a white solid of 2-(2,4-dichloro-5-propargyloxyphenyl)-5,6-dihydroimidazo [1,5-a] pyridine-1,3[2H, 7H]-dione (0.41 g, yield:73.2%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05883049
Source datasetuspto-grants-1999_03
ORD IDord-8310bb03dfa34c02b622907b0e4bdc89
Source noteuspto-grants-1999_03