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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1364654Generated: November 1, 2026

Trimethyltin chloride → 5-Chloro-2-(trimethylstannyl)pyridine

https://huagongshe.com/reaction/1364654

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethyltin chlorideHCID 14016—
Reactant5-Chloropyridin-2-yl trifluoromethanesulfonateHCID 11780288—
Product5-Chloro-2-(trimethylstannyl)pyridineHCID 21942643—

Reaction Steps

5-chloropyridin-2-yl trifluoromethanesulfonate (4.12 mmol) was used in Procedure I with trimethyltin chloride to yield 5-chloro-2-(trimethylstannyl)pyridine. The crude material (˜4 mmol) was used in Procedure K with N-(4-chloro-3-iodophenyl)-2-methyl-6-(trifluoromethyl)nicotinamide (2 mmol). Purified by silica gel chromatography (0-50% ethyl acetate/hexane) to yield N-(4-chloro-3-(5-chloropyridin-2-yl)phenyl)-2-methyl-6-(trifluoromethyl)nicotinamide as a white solid: TLC Rf=0.48 (25% ethyl acetate/hexanes); MS (Q1) 427 (M)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07888364B2
Source datasetuspto-grants-2011_02
ORD IDord-eded0223113d49f294f6125fb27aeb70
Source noteuspto-grants-2011_02