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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 570825Generated: October 31, 2026

Hydrochloric Acid → HCID 178469942, compound

https://huagongshe.com/reaction/570825

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 59580024HCID 59580024—
SolventDimethylformamideHCID 6228—
ProductHCID 178469942HCID 178469942—

Reaction Conditions

Temperature40 °C

Reaction Steps

A suspension of 1-acetyl-3-oxo-2,3-dihydro-1H-pyrazole-4-carboxilic acid ethyl ester (2.7 g, This compound was prepared in a similar manner to that described in Bioorganic & Medicinal Chemistry Letters (2002), 12 (16), 2105-2108), benzylbromide (2.5 g), potassium carbonate (2.1 g) in N,N-dimethylformamide (20 mL) was stirred at 40° C. for 20 hours. To this reaction mixture was added 1 mol/L hydrochloric acid, and this mixture was extracted with ethyl acetate. This organic layer was washed with brine, and dried over anhydrous magnesium sulfate. The solvent was removed under reduced pressure. The residue was purified by column chromatography on aminopropyl silica gel (eluent: ethyl acetate/n-hexane) to give the title compound (1.6 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09023882B2
Source datasetuspto-grants-2015_05
ORD IDord-475e135ec9c34086a49d5266217b29c3
Source noteuspto-grants-2015_05