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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 475584Generated: October 30, 2026

HCID 57855745, compound → HCID 68981884, compound

https://huagongshe.com/reaction/475584

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 57855745HCID 57855745—
CatalystHCID 178418390HCID 178418390—
SolventEthanolHCID 702—
ProductHCID 68981884HCID 68981884—

Reaction Steps

A 0.3 g quantity of 3-{2-[3-(2-cyclohexenyloxy)-4-methoxyphenyl]oxazol-4-yl}-1-(3-methylpyridin-2-yl)propan-1-one obtained in Example 157 was dissolved in 20 ml of ethanol. A 50 mg quantity of 10% palladium-carbon powder was added thereto, and the mixture was stirred at room temperature for 2 hours. The catalyst was removed by filtration, and the filtrate was then concentrated. The obtained residue was purified by silica gel column chromatography (n-hexane:ethyl acetate=3:1) to give 0.2 g of pale yellow oily 3-[2-(3-cyclohexyloxy-4-methoxyphenyl)oxazol-4-yl]-1-(3-methylpyridin-2-yl)propan-1-one.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08637559B2
Source datasetuspto-grants-2014_01
ORD IDord-fee3aebfeecf4adcbdedd55e2484eb4a
Source noteuspto-grants-2014_01