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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 5-Bromopyrazine-2,3-diamine | HCID 2771857 | — |
| Reactant | Hexabutyldistannane | HCID 6327815 | — |
| Reactant | 1-(2-fluorobenzyl)-3-iodo-1H-pyrazolo(3,4-b)pyridine | HCID 57415891 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 5-[1-(2-Fluorobenzyl)-1H-pyrazolo[3,4-b]pyridin-3-yl]pyrazine-2,3-diamine | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09096592B2 |
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| Source dataset | uspto-grants-2015_08 |
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| ORD ID | ord-819c6b4e5b8547bd97d93575c16236a6 |
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| Source note | uspto-grants-2015_08 |
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