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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2199611Generated: October 30, 2026

Sodium Carbonate → 5-(5-Bromo-3-pyridyl)-1H-tetrazole

https://huagongshe.com/reaction/2199611

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantTriphenylphosphineHCID 11776—
Reactant5-(5-Bromo-3-pyridyl)-1H-tetrazoleHCID 4173761—
Reactant2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzo[b]thiophen-5-amineHCID 125467728—
Catalystpalladium(II) acetateHCID 167845—
Solvent1,4-DioxaneHCID 31275—
Product5-(5-Bromo-3-pyridyl)-1H-tetrazoleHCID 4173761—
Product2-(5-(2H-tetrazol-5-yl)pyridin-3-yl)benzo[b]thiophen-5-amineHCID 121268931—

Reaction Conditions

Temperature100 °C

Reaction Steps

The reaction mixture of 3-bromo-5-(2H-tetrazol-5-yl)pyridine (226 mg, 1.0 mmol, 1 eq), 2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzo[b]thiophen-5-amine (316 mg, 1.15 eq), triphenylphosphine (53 mg, 0.2 eq), and palladium diacetate (22 mg, 0.1 eq) in dioxane (3 mL) and aqueous sodium carbonate (2 M, 2 mL, 4 eq) under nitrogen atmosphere was vigorously stirred and heated at 100° C. for three hours. It was then cooled to room temperature, filtered through a Buchner funnel, and rinsed with small amount of water and ethyl acetate. The filtrate was isolated and concentrated down with silica gel. Upon a gradient column chromatography (EtOAc to MeOH-EtOAc 1:4), 2-(5-(2H-tetrazol-5-yl)pyridin-3-yl)benzo[b]thiophen-5-amine was obtained as an orange colored solid in the amount of 92 mg while the starting material, 3-bromo-5-(2H-tetrazol-5-yl)pyridine was recovered in the amount of 90 mg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09359336B2
Source datasetuspto-grants-2016_06
ORD IDord-41dc2c2c35014a42b20ec36035e1afff
Source noteuspto-grants-2016_06