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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1361850Generated: October 26, 2026

Water → N-[4-(2-Furyl)-5-(tetrahydropyran-4-ylcarbonyl)thiazol-2-yl]-2-(trifluoromethoxy)benzamide

https://huagongshe.com/reaction/1361850

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant2-(Trifluoromethoxy)benzoyl ChlorideHCID 2777241—
Reactant2-Amino-4-(2-furyl)-5-(tetrahydropyran-4-ylcarbonyl)thiazoleHCID 86612468—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventPyridineHCID 1049—
ProductN-[4-(2-Furyl)-5-(tetrahydropyran-4-ylcarbonyl)thiazol-2-yl]-2-(trifluoromethoxy)benzamideHCID 2314420853%

Reaction Conditions

Temperature80 °C

Reaction Steps

Compound 454 (125 mg, 0.450 mmol) and DMAP (0.022 mmol) were suspended in pyridine (2 mL), and 2-(trifluoromethoxy)benzoyl chloride (202 mg, 0.900 mmol) was added thereto, followed by stirring at 80° C. for 6 hours. The reaction mixture was poured into water, followed by extraction with ethyl acetate. The organic layer was washed with a saturated aqueous solution of sodium chloride and dried over anhydrous magnesium sulfate, and then the solvent was distilled away under reduced pressure. The resulting residue was recrystallized from ethanol to afford the entitled Compound 475 (111 mg, 53%) as a pale yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07880013B2
Source datasetuspto-grants-2011_02
ORD IDord-046d931f7d9d49d98f491b6b6ea9baf6
Source noteuspto-grants-2011_02