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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 246027Generated: October 30, 2026

Tributyltin Chloride → 6-tert-butyl-1-methyl-3-tributylstannanyl-1H-indazole

https://huagongshe.com/reaction/246027

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTributyltin ChlorideHCID 15096—
Reactant6-(tert-Butyl)-3-iodo-1-methyl-1H-indazoleHCID 71279953—
ReactantHCID 178418918HCID 178418918—
SolventTetrahydrofuranHCID 8028—
Product6-tert-butyl-1-methyl-3-tributylstannanyl-1H-indazoleHCID 71280106—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 6-tert-butyl-3-iodo-1-methyl-1H-indazole (150 mg, 0.45 mmol) in THF (3 mL) at 0° C. was slowly added isopropylmagnesium chloride (2.0 M in THF, 0.27 mL, 0.54 mmol). The bright yellow heterogeneous reaction mixture was stirred at 0° C. for 1 h then tributylchlorostannane (0.15 mL, 0.54 mmol) was added dropwise. Stirring was continued at 0° C. for 20 min then at room temperature for 3 h. The reaction mixture was quenched with water and extracted with EtOAc (2×). The combined organics were washed with brine then dried over MgSO4 and concentrated to afford 6-tert-butyl-1-methyl-3-tributylstannanyl-1H-indazole as a viscous yellow oil which was 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-1c673ba749194d31b97dcc6cd2cd285d
Source noteuspto-grants-2014_02