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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 246768Generated: October 28, 2026

Tributyltin Chloride → 5-isopropyl-1-methyl-3-(tributylstannyl)-1H-indazole

https://huagongshe.com/reaction/246768

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTributyltin ChlorideHCID 15096—
Reactant3-iodo-5-isopropyl-1-methyl-1H-indazoleHCID 71280366—
ReactantHCID 178418918HCID 178418918—
SolventTetrahydrofuranHCID 8028—
Product5-isopropyl-1-methyl-3-(tributylstannyl)-1H-indazoleHCID 71280336—

Reaction Conditions

Temperature-16 °C

Reaction Steps

To a stirred solution of 3-iodo-5-isopropyl-1-methyl-1H-indazole (0.3 g, crude) in 100 mL of dry THF at −16° C. under nitrogen was added i-PrMgCl (0.69 mL, 1.38 mmol, 2M in THF) drop-wise. Then the mixture was stirred at −16° C. for 20 minutes. Tributylchlorostannane (0.39 g, 1.2 mmol) was added slowly and the mixture was stirred at room temperature for 2.5 hours. The solution was quenched by 40 mL of water, extracted with ethyl acetate (2×100 mL), washed with water (2×50 mL), brine (50 mL) and dried over anhydrous sodium sulfate. The drying agent was removed by filtration and the filtrate was evaporated under reduced pressure to give crude 5-isopropyl-1-methyl-3-(tributylstannyl)-1H-indazole as an oil, which was used into next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08658646B2
Source datasetuspto-grants-2014_02
ORD IDord-f1b1c0a617c5455eb71e5632e3fd3250
Source noteuspto-grants-2014_02