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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2092055Generated: November 1, 2026

Ethyl bromoacetate → HCID 68431289, compound

https://huagongshe.com/reaction/2092055

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromoacetateHCID 7748—
ReactantPotassium CarbonateHCID 11430—
ReactantAmmonium ChlorideHCID 25517—
ReactantHCID 68429305HCID 68429305—
SolventDimethylformamideHCID 6228—
ProductHCID 68431289HCID 6843128988.3%

Reaction Conditions

Temperature80 °C

Reaction Steps

4-Bromo-5-[(1R,2R,3R,5S)-2,6,6-trimethylbicyclo[3.1.1]hept-3-ylamino]pyridazin-3(2H)-one (600 mg, 1.84 mmol) in N,N-dimethylformamide (6 mL) was mixed with ethyl bromoacetate (306 μL, 2.76 mmol) and potassium carbonate (381 mg, 2.76 mmol) at room temperature and stirred at 80° C. for 1.5 hours. After cooling, the reaction solution was mixed with saturated aqueous ammonium chloride and extracted with ethyl acetate. The resulting organic layer was washed with saturated aqueous ammonium chloride and saturated aqueous sodium chloride, dried over anhydrous magnesium sulfate and evaporated under reduced pressure. The resulting residue was purified by silica gel chromatography (chloroform/ethyl acetate=8/1) to give the desired product (670 mg, 88% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08440666B2
Source datasetuspto-grants-2013_05
ORD IDord-a79528d8385c41c994c92cee533b13be
Source noteuspto-grants-2013_05