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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1257392Generated: November 2, 2026

Pyridine → ethyl 1-[(4-{3-[(Z)-2-pyridin-3-ylethenyl]-5-(trifluoromethyl)phenyl}-1,3-thiazol-2-yl)methyl]-1H-pyrazole-4-carboxylate

https://huagongshe.com/reaction/1257392

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactantethyl 1-({4-[3-(pyridin-3-ylethynyl)-5-(trifluoromethyl)phenyl]-1,3-thiazol-2-yl}methyl)-1H-pyrazole-4-carboxylateHCID 66939083—
CatalystPalladium barium sulphateHCID 17887766—
SolventEthanolHCID 702—
Productethyl 1-[(4-{3-[(Z)-2-pyridin-3-ylethenyl]-5-(trifluoromethyl)phenyl}-1,3-thiazol-2-yl)methyl]-1H-pyrazole-4-carboxylateHCID 6693931846.4%

Reaction Steps

To a solution (10 mL) of the compound (980 mg, 2.0 mmol) obtained in Example 87a in ethanol were added pyridine (480 mg, 6.1 mmol) and palladium-barium sulfate (490 mg), and the mixture was stirred at room temperature for 5 hr under a hydrogen atmosphere (1 atm). Palladium-carbon was removed and the solvent was evaporated under reduced pressure. The resulting crude title compound was purified by column chromatography (hexane-hexane/ethyl acetate=35/65) to give the title compound (450 mg, 46%) as colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08461348B2
Source datasetuspto-grants-2013_06
ORD IDord-0d413d4dfbc74b65a09a84867d2fa534
Source noteuspto-grants-2013_06