Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 246325Generated: October 27, 2026

Tributyltin Chloride → 6-methanesulfonyl-1-methyl-3-tributylstannanyl-1H-indazole

https://huagongshe.com/reaction/246325

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTributyltin ChlorideHCID 15096—
Reactant3-Iodo-1-methyl-6-(methylsulfonyl)-1H-indazoleHCID 71279808—
ReactantHCID 178418918HCID 178418918—
SolventTetrahydrofuranHCID 8028—
Product6-methanesulfonyl-1-methyl-3-tributylstannanyl-1H-indazoleHCID 71280160—

Reaction Conditions

Temperature-16 °C

Reaction Steps

In a round-bottomed flask, 3-iodo-6-methanesulfonyl-1-methyl-1H-indazole (120 mg, 0.36 mmol) was dissolved in THF (2 ml). The colorless solution was cooled to −16° C. (NaCl/ice bath) and isopropylmagnesium chloride (2.0 M in THF, 0.25 ml, 0.50 mmol) was added dropwise. The reaction mixture was stirred at −16° C. for 1 h then tributylchlorostannane (0.12 ml, 0.44 mmol) was slowly added. The reaction mixture was allowed to warm to room temperature over 2.5 h then quenched with saturated NH4Cl-solution and extracted with EtOAc (2×). The combined organic layers were washed with water and brine then dried over sodium sulfate, filtered and concentrated to afford 6-methanesulfonyl-1-methyl-3-tributylstannanyl-1H-indazole as a light yellow oil which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08658646B2
Source datasetuspto-grants-2014_02
ORD IDord-a16565b00bac42ac9e9ca31e6cc7f466
Source noteuspto-grants-2014_02