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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1888796Generated: November 1, 2026

5-Iodo-6-methyl-N-[4-(methylsulfonyl)benzyl]-2-oxo-1-[3-(trifluoro-methyl)phenyl]1,2-dihydropyridine-3-carboxamide → HCID 66725302, compound

https://huagongshe.com/reaction/1888796

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Iodo-6-methyl-N-[4-(methylsulfonyl)benzyl]-2-oxo-1-[3-(trifluoro-methyl)phenyl]1,2-dihydropyridine-3-carboxamideHCID 11519933—
Reactant2-(Tri-n-butylstannyl)oxazoleHCID 15486183—
CatalystHCID 178418397HCID 178418397—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductHCID 66725302HCID 6672530267%

Reaction Conditions

Temperature100 °C

Reaction Steps

5-Iodo-6-methyl-N-[4-(methylsulfonyl)benzyl]-2-oxo-1-[3-(trifluoro-methyl)phenyl]-1,2-dihydropyridine-3-carboxamide (0.10 g, 0.169 mmol), 2-tributylstannyl-oxazole (0.12 g, 0.33 mmol, prepared according to literature procedures), Pd(PPh3)4 (0.015 g, 0.012 mmol) and dimethoxyethane (DME, 2.5 ml) and a magnetic stirrer bar were placed in a vial. The suspension was degassed and the vial sealed, and subsequently heated (100° C.) with stirring for 4 h. LC-MS confirmed the conversion of the iodide to the desired product, and the solvents were removed in vacuo. Purification on preparative HPLC afforded the title compound (0.06 g, 67%) as a white solid after freeze-drying the pure fractions.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08501784B2
Source datasetuspto-grants-2013_08
ORD IDord-70e98f4e01044df1913c4ce5e9bd26f4
Source noteuspto-grants-2013_08