Back
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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Bromo-3-fluoro-6-methylpyridineHCID 24820318—
Reactant2-(2-Bromopyridin-4-yl) isoindoline-1,3-dioneHCID 86704364—
ReactantHCID 178418306HCID 178418306—
CatalystZincchlorideHCID 3007855—
CatalystHCID 178418397HCID 178418397—
SolventTetrahydrofuranHCID 8028—
Product2-(3'-Fluoro-6'-methyl-2,2'-bipyridin-4-yl)isoindoline-1,3-dioneHCID 6747051444.8%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09073918B2
Source datasetuspto-grants-2015_07
ORD IDord-2c81fe2701734e5c9646c0d6bf4fcac9
Source noteuspto-grants-2015_07