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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 510050Generated: October 26, 2026

5-Bromopyrazine-2,3-diamine → 5-[1-(2-Fluorobenzyl)-1H-pyrazolo[3,4-b]pyridin-3-yl]pyrazine-2,3-diamine

https://huagongshe.com/reaction/510050

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Bromopyrazine-2,3-diamineHCID 2771857—
ReactantHexabutyldistannaneHCID 6327815—
Reactant1-(2-fluorobenzyl)-3-iodo-1H-pyrazolo(3,4-b)pyridineHCID 57415891—
CatalystHCID 178418476HCID 178418476—
Solvent1,4-DioxaneHCID 31275—
Product5-[1-(2-Fluorobenzyl)-1H-pyrazolo[3,4-b]pyridin-3-yl]pyrazine-2,3-diamineHCID 66614338—

Reaction Steps

Under argon, 425 mg (1.20 mmol) of the compound from Example 33A were initially charged in 1,4-dioxane (11 ml), and the reaction mixture was purged with argon for 10 min. Thereafter, 0.91 ml (1.80 mmol) of hexabutylditin and 250 mg (1.32 mmol) of 2,3-diamino-5-bromopyrazine were added. Subsequently, 422 mg (0.60 mmol) of bis(triphenylphosphine)palladium(II) chloride were added and the reaction mixture was heated to reflux overnight. Thereafter, the mixture was cooled to RT and filtered through Celite, and the filtrate was concentrated. The residue was admixed with methanol, and the solids were filtered off and discarded. The filtrate was taken up in methanol-dichloromethane, absorbed onto diatomaceous earth and purified on silica gel (eluent: cyclohexane-ethyl acetate 2:1, 1:1). This gave 151 mg (31% purity, 11% of theory) of the title compound. The crude product was converted further without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09096592B2
Source datasetuspto-grants-2015_08
ORD IDord-819c6b4e5b8547bd97d93575c16236a6
Source noteuspto-grants-2015_08