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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 246376Generated: October 25, 2026

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

https://huagongshe.com/reaction/246376

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTributyltin ChlorideHCID 15096—
Reactant5-(difluoromethoxy)-3-iodo-1-methyl-1H-indazoleHCID 71279544—
ReactantHCID 178418918HCID 178418918—
SolventTetrahydrofuranHCID 8028—
Product5-(Difluoromethoxy)-1-methyl-3-(tributylstannyl)-1H-indazoleHCID 71279627—

Reaction Conditions

Temperature-16 °C

Reaction Steps

5-(Difluoromethoxy)-3-iodo-1-methyl-1H-indazole (0.265 g, 818 μmol) was dissolved in THF (3.00 mL). The colorless solution was cooled to −16° C. (NaCl/ice bath) then isopropylmagnesium chloride (2M in THF, 458 μL, 916 μmol) added dropwise at −16° C. The reaction mixture was stirred at −16° C. for 20 min then tributylchlorostannane (306 mg, 255 μL, 940 μmol) was added slowly. The reaction mixture was warmed to 25° C. and stirred for 1.5 h. The reaction mixture was quenched with saturated ammonium chloride solution, extracted with dichloromethane (3×30 mL), organics dried over MgSO4 and concentrated to a yellow oil. The residue was dried under high vacuum and taken into next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08658646B2
Source datasetuspto-grants-2014_02
ORD IDord-ade00f536a8e4f59869b3e4da9cb8039
Source noteuspto-grants-2014_02