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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1292112Generated: November 2, 2026

HCID 18914232, compound → HCID 18914218, compound

https://huagongshe.com/reaction/1292112

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 18914232HCID 18914232—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductHCID 18914218HCID 1891421889.5%

Reaction Steps

1-(4-benzyloxy-3-isobutylbenzoyl)-4-isobutylpiperazine (6.78 g) was dissolved in ethanol (250 ml) and then, with 10% palladium charcoal (0.14 g) added thereto, the mixture was stirred at room temperature for 24 hours in a hydrogen gas atmosphere. After the reaction mixture was filtered under a suction, the filtrate was concentrated under a vacuum, thereby yielding 4.73 g of 1-(4-hydroxy-3-isobutylbenzoyl)-4-isobutylpiperazine. In acetone (50 ml), this compound (0.96 g), 2-fluorobenzyl bromide (0.68 g), and potassium carbonate (0.83 g) of were refluxed with stirring for 4 hours. The reaction mixture, with water added thereto, was extracted with ethyl acetate. The extract was washed with saturated aqueous sodium hydrogencarbonate solution and saturated brine successively, and then dried over sodium sulfate anhydride. The residue obtained after concentration was purified by silica gel column chromatography (ethyl acetate:n-hexane=1:2), thereby yielding 0.90 g of the aimed compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05756505
Source datasetuspto-grants-1998_05
ORD IDord-54e77404d171439fbe131640cf805065
Source noteuspto-grants-1998_05