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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1374157Generated: October 31, 2026

Sodium Bicarbonate → HCID 21075865, compound

https://huagongshe.com/reaction/1374157

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
ReactantPotassium AcetateHCID 517044—
ReactantBis(pinacolato)diboraneHCID 2733548—
Reactant5-Chloropyridin-3-yl trifluoromethanesulfonateHCID 15185870—
Reactant5-(2-Fluoro-6-iodophenyl)-2-methyl-2H-tetrazoleHCID 16102901—
CatalystBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
SolventDimethylformamideHCID 6228—
ProductHCID 21075865HCID 21075865—

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 5-chloropyridin-3-yl trifluoromethanesulfonate (6.00 g, 22.9 mmol), bis(pinacolato)diboron (6.12 g, 24.1 mmol), potassium acetate (6.75 g, 68.8 mmol), and [1,1′-bis-(diphenylphosphino)ferrocene]palladium(II) dichloride (0.60 g, 0.82 mmol) in 30 mL DMF was heated to 80° C. under N2 for 2 hours. The reaction mixture was cooled to room temperature, and 5-(2-fluoro-6-iodophenyl)-2-methyl-2H-tetrazole (4.88 g, 16.1 mmol), sodium bicarbonate (2M, 34.4 mL, 68.8 mmol), and [1,1′-bis(diphenylphosphino)ferrocene]palladium(II) dichloride (0.60 g, 0.82 mmol) were added. The reaction mixture was heated to 80° C. overnight, then cooled to room temperature and partitioned between ethyl acetate and water. The organic extract was washed with water and brine, dried over Na2SO4, filtered and concentrated under vacuum. The residue was subjected to silica gel chromatography eluted with 0–30% ethyl acetate in hexanes to provide 3-chloro-5-[3-fluoro-2-(2-methyl-2H-tetrazol-5-yl)phenyl]pyridine that gave proton NMR spectra consistent with theory and a mass ion (ES+) of 290.11 for M+H+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07163951B2
Source datasetuspto-grants-2007_01
ORD IDord-e81b485628114c8f8dc3941b4f58b8c8
Source noteuspto-grants-2007_01