HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1914937Generated: October 31, 2026
2,6-Dichloropyrazine → HCID 86673735, compound
https://huagongshe.com/reaction/1914937
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,6-Dichloropyrazine | HCID 78504 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 53344730 | HCID 53344730 | — |
| Catalyst | Dichlorobis(triphenylphosphine)palladium | HCID 6102075 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 86673735 | HCID 86673735 | — |
Reaction Steps
A solution of 302 mg (1.00 mmol) 2-(5-chloro-2-fluoro-phenyl)-[1,8]naphthyridine-4-boronic acid, 194 mg (1.30 mmol) 2,6-dichloropyrazine and 101 mg (1.2 mmol) sodium bicarbonate in 4 ml DMF and 1 ml water was heated to 80° C. under nitrogen. Then 14.0 mg (0.02 mmol) bis-(triphenylphosphine)-palladium(II)-chloride were added and the reaction mixture was stirred for 16 hours at 80° C. Water was added to the reaction mixture and the resulting precipitate was filtered off. The residue was chromatographed on a silica gel column with dichloromethane/methanol as eluent yielding 2-(5-chloro-2-fluoro-phenyl)-4-(6-chloro-pyrazin-2-yl)-[1,8]naphthyridine as colourless crystals; HPLC-MS: 2.35 min, [M+H] 371.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08614226B2 |
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| Source dataset | uspto-grants-2013_12 |
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| ORD ID | ord-60776e833f9e4ad4969ec4bb893cd250 |
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| Source note | uspto-grants-2013_12 |
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