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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 57938Generated: October 27, 2026

N,N'-Dimethylethylenediamine → [2-Fluoro-6-[6-(6-methylpyrazin-2-yl)pyrazolo[4,3-c]pyridin-1-yl]-3-pyridyl]methanol

https://huagongshe.com/reaction/57938

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N'-DimethylethylenediamineHCID 8070—
ReactantPotassium CarbonateHCID 11430—
Reactant(6-Bromo-2-fluoropyridin-3-YL)methanolHCID 71303921—
Reactant6-(6-methylpyrazin-2-yl)-1H-pyrazolo[4,3-c]pyridineHCID 86707080—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
Solvent1,4-DioxaneHCID 31275—
Product[2-Fluoro-6-[6-(6-methylpyrazin-2-yl)pyrazolo[4,3-c]pyridin-1-yl]-3-pyridyl]methanolHCID 8670712312%

Reaction Conditions

Temperature105 °C

Reaction Steps

A mixture of 6-(6-methylpyrazin-2-yl)-1H-pyrazolo[4,3-c]pyridine (2.000 mmol; 422.4 mg), (6-bromo-2-fluoro-3-pyridyl)methanol (2.400 mmol; 494.4 mg), potassium carbonate (4.000 mmol; 552.8 mg), copper(I) iodide (2.000 mmol; 380.9 mg), and N,N′-Dimethylethylenediamine (0.2000 mmol; 17.81 mg; 0.0217 mL) in 1,4-Dioxane (15 mL) was purged with Argon then sealed in a pressure tube and heated at 105° C. overnight. The mixture was cooled to room temperature and filtered through Celite. The filtrate was concentrated and the residue was purified on silica eluted with 0 to 100% EtOAc in Heptane to afford [2-fluoro-6-[6-(6-methylpyrazin-2-yl)pyrazolo[4,3-c]pyridin-1-yl]-3-pyridyl]methanol (79.5 mg, 12%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09434725B2
Source datasetuspto-grants-2016_09
ORD IDord-e7b5c56221d54b3eb30976beb6a48aab
Source noteuspto-grants-2016_09