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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 888406Generated: October 30, 2026

Diisopropylamine → Methyl 3-bromo-5-(5-chloropyridin-2-yl)benzoate

https://huagongshe.com/reaction/888406

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylamineHCID 7912—
Reactant2-Bromo-5-chloropyridineHCID 817098—
ReactantTrisodium 3,3',3''-phosphinetriyltris(benzene-1-sulphonate)HCID 6099338—
ReactantMethyl 3-bromo-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-YL)benzoateHCID 53436914—
Catalystpalladium(II) acetateHCID 167845—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductMethyl 3-bromo-5-(5-chloropyridin-2-yl)benzoateHCID 6664992982.4%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of methyl 3-bromo-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate (0.10 g, 0.29 mmol) in DMF (1.5 mL) and water (0.49 mL) were added 2-bromo-5-chloropyridine (0.17 g, 0.88 mmol), palladium(II) aceate (3.3 mg, 0.015 mmol), 3,3′3″-phosphinidynetris(benzenesulfonic acid)trisodium salt (25.0 mg, 0.044 mmol) and diisopropylamine (0.10 mL, 0.73 mmol). The mixture was heated to 80° C. After 1 h, the mixture was filtered and the filtrate was purified by reverse phase chromatography (C-18, 85% water/acetonitrile→5% water/acetonitrile with 0.1% trifluoroacetic acid) gave the title compound (78 mg). MS 326.0 (M).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08247401B2
Source datasetuspto-grants-2012_08
ORD IDord-87cd173fdbd94afd9aff1f93b1854bce
Source noteuspto-grants-2012_08