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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 446924Generated: October 30, 2026

Tetrabutylammonium Fluoride → N-[3-(1-Methyl-1H-pyrazolo[3,4-c]pyridin-4-ylethynyl)-phenyl]-benzamide

https://huagongshe.com/reaction/446924

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrabutylammonium FluorideHCID 2724141—
Reactant4-Bromo-1-methyl-1H-pyrazolo(3,4-c)pyridineHCID 57606936—
ReactantHCID 67399535HCID 67399535—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418476HCID 178418476—
SolventTetrahydrofuranHCID 8028—
ProductN-[3-(1-Methyl-1H-pyrazolo[3,4-c]pyridin-4-ylethynyl)-phenyl]-benzamideHCID 59536452—

Reaction Conditions

Temperature80 °C

Reaction Steps

In an adaption of GP 3c, 60 mg of 4-bromo-1-methyl-1H-pyrazolo[3,4-c]pyridine (Intermediate 2.1, 0.28 mmol, 1 eq), 140 mg N-(3-trimethylsilanylethynyl-phenyl)-benzamide (0.48 mmol, 1.68 eq.), 10 mg dichlorobis(triphenylphosphine)palladium (II) (PdCl2(PPh3)2) (0.014 mmol, 5 mol %) and 10.8 mg copper (I) iodide (0.057 mmol, 0.2 eq.) were dissolved in 1.4 mL THF (0.2 M) and treated with 0.35 mL tetra-n-butylammonium fluoride solution (1.0 M in THF, 0.35 mmol, 1.25 eq.). The resulting mixture was heated to 80° C. in a Biotage Initiator microwave oven for 30 min. Extractive work-up followed by column chromatography and preparative HPLC purification provided the target compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08481539B2
Source datasetuspto-grants-2013_07
ORD IDord-4356746b20724ab586c8f0354645e551
Source noteuspto-grants-2013_07