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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 246605Generated: October 30, 2026

Tributyltin Chloride → 1-Methyl-3-(tributylstannyl)-1H-indazole-6-carbonitrile

https://huagongshe.com/reaction/246605

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTributyltin ChlorideHCID 15096—
Reactant3-Iodo-1-methyl-1H-indazole-6-carbonitrileHCID 71279438—
Reactant3-iodo-2-methyl-1H-indazole-6-carbonitrileHCID 86677997—
ReactantHCID 178418918HCID 178418918—
SolventTetrahydrofuranHCID 8028—
Product1-Methyl-3-(tributylstannyl)-1H-indazole-6-carbonitrileHCID 71279843—

Reaction Conditions

Temperature-40 °C

Reaction Steps

A mixture 3-iodo-1-methyl-1H-indazole-6-carbonitrile and 3-iodo-2-methyl-1H-indazole-6-carbonitrile (160 mg, 0.565 mmol) was dissolved in THF (6 mL). The solution was cooled to −40° C. Isopropylmagnesium chloride 2M in THF (0.34 mL, 0.678 mmol) was added drop-wise at −40° C. The reaction mixture was stirred at −40° C. for 20 min, then chlorotributyltin (0.18 mL, 0.678 mmol) was added slowly. The reaction mixture was allowed to warm to room temperature and stirred for 1.5 h. The reaction mixture was quenched with saturated NH4Cl solution and then extracted with EtOAc (3×10 mL), combined organics were washed with water (10 mL), brine (10 mL), dried over Na2SO4 and concentrated. The residue was used in the next step without further treatment.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08658646B2
Source datasetuspto-grants-2014_02
ORD IDord-ce38cc997e1b4fd0b4b5f63bd71ae258
Source noteuspto-grants-2014_02