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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2221542Generated: November 3, 2026

HCID 23076431, compound → HCID 69217575, compound

https://huagongshe.com/reaction/2221542

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 23076431HCID 23076431—
CatalystPalladiumHCID 23938—
SolventTetrahydrofuranHCID 8028—
ProductHCID 69217575HCID 6921757571.2%

Reaction Steps

4-[(E)-2-(3-Benzyloxy-1-phenyl-1H-pyrazol-4-yl)ethenyl]-1,3-thiazole (0.81 g), 5% palladium on carbon (0.80 g) and tetrahydrofuran (80 mL) were subjected to catalytic reduction under a hydrogen atmosphere and atmospheric pressure. The catalyst was filtered off and the filtrate was concentrated. The residue was subjected to silica gel column chromatography, and eluted with ethyl acetate-hexane (1:3, v/v) to give 4-[2-(3-benzyloxy-1-phenyl-1H-pyrazol-4-yl)ethyl]-1,3-thiazole as a colorless oil (0.58 g, yield 70%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07368578B2
Source datasetuspto-grants-2008_05
ORD IDord-4e627219ed024e21b809bff6801ba15b
Source noteuspto-grants-2008_05