HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1522549Generated: October 29, 2026
2-Bromo-3-fluoro-6-methylpyridine → 2-(3'-Fluoro-6'-methyl-2,2'-bipyridin-4-yl)isoindoline-1,3-dione
https://huagongshe.com/reaction/1522549
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Bromo-3-fluoro-6-methylpyridine | HCID 24820318 | — |
| Reactant | 2-(2-Bromopyridin-4-yl) isoindoline-1,3-dione | HCID 86704364 | — |
| Reactant | HCID 178418306 | HCID 178418306 | — |
| Catalyst | Zincchloride | HCID 3007855 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(3'-Fluoro-6'-methyl-2,2'-bipyridin-4-yl)isoindoline-1,3-dione | HCID 67470514 | 44.8% |
Reaction Steps
Tetrahydrofuran (10 mL) was cooled to −78° C. and tert-Butyllithium (4.56 ml, 6.84 mmol) was added, followed by a solution of 2-bromo-3-fluoro-6-methylpyridine (1 g, 5.26 mmol) in tetrahydrofuran (2.5 mL). The reaction mixture was stirred for 30 minutes then zinc(II)chloride (2.58 g, 18.95 mmol) was added and the reaction was warmed to room temperature over 2 hours. A solution of 2-(2-bromopyridin-4-yl) isoindoline-1,3-dione (9) (1.595 g, 5.26 mmol) and tetrakis(triphenylphosphine)palladium(0) (0.608 g, 0.526 mmol) in THF (10 mL) was added and the reaction was stirred at room temperature over night to give a solid which was collected by filtration to give 2-(3′-fluoro-6′-methyl-2,2′-bipyridin-4-yl)isoindoline-1,3-dione as a white solid (786 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09073918B2 |
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| Source dataset | uspto-grants-2015_07 |
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| ORD ID | ord-2c81fe2701734e5c9646c0d6bf4fcac9 |
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| Source note | uspto-grants-2015_07 |
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