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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 245963Generated: October 27, 2026

Tributyltin Chloride → 5,6-dichloro-1-methyl-3-tributylstannanyl-1H-indazole

https://huagongshe.com/reaction/245963

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTributyltin ChlorideHCID 15096—
Reactant5,6-dichloro-3-iodo-1-methyl-1H-indazoleHCID 71279635—
ReactantHCID 178418918HCID 178418918—
SolventTetrahydrofuranHCID 8028—
Product5,6-dichloro-1-methyl-3-tributylstannanyl-1H-indazoleHCID 71279490—

Reaction Conditions

Temperature-10 °C

Reaction Steps

To a solution of 5,6-dichloro-3-iodo-1-methyl-1H-indazole (150 mg, 0.44 mmol) in THF (3 mL) at −10° C. (ice/acetone) was slowly added isopropylmagnesium chloride (2.0 M in THF, 0.26 mL, 0.52 mmol). The bright yellow heterogeneous reaction mixture was stirred at −10° C. for 15 min then tributylchlorostannane (0.14 mL, 0.52 mmol) was added dropwise. Stirring was continued at −10° C. for 30 min then at room temperature for 1 h. The reaction mixture was quenched with water and extracted with EtOAc (2×). The combined organics were dried over MgSO4 and concentrated to afford 5,6-dichloro-1-methyl-3-tributylstannanyl-1H-indazole as a pale 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-e37eac3152f04b6f9efcefaa2c52da73
Source noteuspto-grants-2014_02