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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 559795Generated: October 30, 2026

1-Methyl-2-(tributylstannyl)-1H-imidazole → HCID 66725529, compound

https://huagongshe.com/reaction/559795

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Methyl-2-(tributylstannyl)-1H-imidazoleHCID 2763252—
Reactant5-Iodo-6-methyl-N-[4-(methylsulfonyl)benzyl]-2-oxo-1-[3-(trifluoro-methyl)phenyl]1,2-dihydropyridine-3-carboxamideHCID 11519933—
CatalystHCID 178418397HCID 178418397—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductHCID 66725529HCID 6672552910%

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 (0.06 g, 0.1 mmol), 1-methyl-2-tributylstannyl-1H-imidazole (0.11 g, 0.5 mmol, prepared according to literature procedures), Pd(PPh3)4 (0.015 g, 0.012 mmol), DME (2 ml) and a magnetic stirrer bar were placed in a vial. The suspension was degassed and the vial was sealed, and subsequently heated (100° C.) with stirring overnight. 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 (0.005 g, 10%) as a white solid after freeze-drying the pure fractions.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08063073B2
Source datasetuspto-grants-2011_11
ORD IDord-953dfaf7ecaa48d59f2b23276bc24d6c
Source noteuspto-grants-2011_11