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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1845221Generated: October 31, 2026

5-Methyl-2-(tri-n-butylstannyl)pyridine → 3-(5-Methylpyridin-2-yl)-N-((6-methylpyridin-3-yl)methyl)-5-(methylsulfonyl)benzamide

https://huagongshe.com/reaction/1845221

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Methyl-2-(tri-n-butylstannyl)pyridineHCID 11132711—
Reactant3-Bromo-N-((6-methylpyridin-3-yl)methyl)-5-(methylsulfonyl)benzamideHCID 58188265—
CatalystHCID 178418397HCID 178418397—
SolventTolueneHCID 1140—
Product3-(5-Methylpyridin-2-yl)-N-((6-methylpyridin-3-yl)methyl)-5-(methylsulfonyl)benzamideHCID 58188047—

Reaction Steps

A mixture of 3-bromo-N-((6-methylpyridin-3-yl)methyl)-5-(methylsulfonyl)benzamide (71 mg, 0.18 mmol), 5-methyl-2-(tributylstannyl)pyridine (91 mg, 0.23 mmol), tetrakis(triphenylphosphine)palladium(0) (11 mg, 0.0093 mmol) and toluene (2.0 mL) under argon was subjected to microwave irradiation at 120° C. for 2 hours. The mixture was cooled to allow the product to precipitate. The solvent was discarded and the precipitated solids were rinsed with hexane and then purified by preparative HPLC (100×21.2 mm C18 column, 30-70% CH3CN/water[10 mM Et2NH]) to afford a white foam.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08946439B2
Source datasetuspto-grants-2015_02
ORD IDord-b6ea032b039648c49375c1dbf284b3d9
Source noteuspto-grants-2015_02