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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1775071Generated: November 2, 2026

Lithium Chloride → 3-(6-Fluoro-2-pyridinyl)-5-(3-pyridinyl)-1-[[2-(trimethylsilyl)ethoxy]methyl]-1H-pyrazolo[3,4-c]pyridine

https://huagongshe.com/reaction/1775071

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium ChlorideHCID 433294—
Reactant2-Fluoro-6-(tributylstannyl)pyridineHCID 16427115—
ReactantHCID 71253586HCID 71253586—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418397HCID 178418397—
SolventDimethylformamideHCID 6228—
Product3-(6-Fluoro-2-pyridinyl)-5-(3-pyridinyl)-1-[[2-(trimethylsilyl)ethoxy]methyl]-1H-pyrazolo[3,4-c]pyridineHCID 7125405780%

Reaction Conditions

Temperature120 °C

Reaction Steps

To a mixture of 3-iodo-5-(pyridin-3-yl)-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-pyrazolo[3,4-c]pyridine (GCP-P3-205-1) (200 mg, 0.44 mmol) and 2-fluoro-6-(tributylstannyl)pyridine (206 mg, 0.53 mmol) in 3 mL DMF, was added TEA 1 mL, LiCl (56 mg, 1.32 mmol) and CuI (84 mg, 0.44 mmol), and Pd(PPh3)4 (254 mg, 0.22 mmol). The reaction mixture was heated at 120° C. under microwave irradiation for 1 h, and the reaction was monitored by LCMS. Upon completion, the reaction mixture was extracted with 100 mL EtOAc, washed with 50 mL brine, and dried. The solvent was distilled off and the crude material was purified via flash chromatography, eluting with 5% to 30% ethyl acetate in heptane to afford 3-(6-fluoropyridin-2-yl)-5-(pyridin-3-yl)-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-pyrazolo[3,4-c]pyridine as a yellow solid (148 mg, 80%). ESI MS m/z=421.1 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09260425B2
Source datasetuspto-grants-2016_02
ORD IDord-0f84ab7376ea431799c00c90f52dbb36
Source noteuspto-grants-2016_02