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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 246596Generated: October 30, 2026

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

https://huagongshe.com/reaction/246596

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

The crude mixture of 3-iodo-1-methyl-1H-indazole-6-carbonitrile and 3-iodo-2-methyl-1H-indazole-6-carbonitrile (97 mg, crude) was dissolved in THF (4 mL). The solution was cooled to −40° C. Isopropylmagnesium chloride (0.21 mL, 0.41 mmol, 2M in THF) was added drop-wise at −40° C. The reaction mixture was stirred at −40° C. for 20 min. Then chlorotributyltin (0.11 mL) 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 (3×5 mL), organics were washed with water (10 mL), brine (2×10 mL) and dried over Na2SO4 and concentrated. The residue was used to the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08658646B2
Source datasetuspto-grants-2014_02
ORD IDord-c12b5c5f33cf4777a126859380a054a3
Source noteuspto-grants-2014_02