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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 245843Generated: October 31, 2026

Tributyltin Chloride → 6-Methyl-1-tributylstannanyl-imidazo[1,5-a]pyridine

https://huagongshe.com/reaction/245843

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTributyltin ChlorideHCID 15096—
Reactant1-Iodo-6-methylimidazo[1,5-A]pyridineHCID 71280646—
ReactantHCID 178418918HCID 178418918—
SolventTetrahydrofuranHCID 8028—
Product6-Methyl-1-tributylstannanyl-imidazo[1,5-a]pyridineHCID 71279932—

Reaction Conditions

Temperature-16 °C

Reaction Steps

In a round-bottomed flask, 1-iodo-6-methyl-imidazo[1,5-a]pyridine (97 mg, 0.38 mmol) was dissolved in THF (3 ml). The solution was cooled to −16° C. (NaCl/ice bath) and isopropylmagnesium chloride (2.0M solution in THF, 0.23 ml, 0.46 mmol) was added dropwise. The reaction mixture was stirred at −16° C. for 20 min then tributylchlorostannane (0.12 ml, 0.44 mmol) was slowly added. The reaction mixture was allowed to warm to room temperature and stirred for 2 h then quenched with saturated aqueous NH4Cl and extracted with EtOAc (2×). The combined organic layers were washed with water and brine then dried over sodium sulfate, filtered and concentrated to provide 6-methyl-1-tributylstannanyl-imidazo[1,5-a]pyridine as a brown oil which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08658646B2
Source datasetuspto-grants-2014_02
ORD IDord-1feed4ef5c28412c9eab9b2e58484143
Source noteuspto-grants-2014_02