Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 246549Generated: October 29, 2026

Tributyltin Chloride → 6-Fluoro-1-tributylstannyl-imidazo[1,5-a]pyridine

https://huagongshe.com/reaction/246549

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTributyltin ChlorideHCID 15096—
Reactant6-Fluoro-1-iodoimidazo[1,5-A]pyridineHCID 71279825—
ReactantHCID 178418918HCID 178418918—
SolventTetrahydrofuranHCID 8028—
Product6-Fluoro-1-tributylstannyl-imidazo[1,5-a]pyridineHCID 71279921—

Reaction Steps

To a −16° C. solution of 6-fluoro-1-iodoimidazo[1,5-a]pyridine (158 mg, 603 μmol) in THF (4.64 mL) was added isopropylmagnesium chloride (368 μL, 736 μmol) dropwise. After 20 min tributylchlorostannane (232 mg, 193 μL, 712 μmol) was added dropwise at −16° C. and allowed to warm to room temperature. After 2 h the reaction was quenched with saturated ammonium chloride and diluted with ethyl acetate. The phases were separated and the organic phase washed with brine. The organic layer was collected, concentrated in vacuo, and used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08658646B2
Source datasetuspto-grants-2014_02
ORD IDord-f52b80281417489eafd43aa4da27b664
Source noteuspto-grants-2014_02