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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 245793Generated: October 25, 2026

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

https://huagongshe.com/reaction/245793

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTributyltin ChlorideHCID 15096—
Reactant6-chloro-3-iodo-1-methyl-1H-indazoleHCID 71279610—
ReactantHCID 178418918HCID 178418918—
SolventTetrahydrofuranHCID 8028—
Product6-chloro-1-methyl-3-tributylstannanyl-1H-indazoleHCID 71280599—

Reaction Conditions

Temperature-16 °C

Reaction Steps

6-Chloro-3-iodo-1-methyl-1H-indazole (108 mg, 0.35 mmol) was dissolved in THF (2 ml) and the solution was cooled to −16° C. using a NaCl/ice bath. Isopropylmagnesium chloride (2.0M in THF, 0.20 ml, 0.40 mmol) was added dropwise and the reaction mixture was stirred at −16° C. for 15 min. Tributylchlorostannane (0.11 ml, 0.40 mmol) was slowly added and the reaction mixture was allowed to warm to room temperature over 1.5 h. The reaction mixture was 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-chloro-1-methyl-3-tributylstannanyl-1H-indazole 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-e4c31799a46b451fabf2a3c8689a1638
Source noteuspto-grants-2014_02