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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1716529Generated: October 25, 2026

2-Amino-4-methylpyridine → (6-Bromopyridin-2-yl)-(4-methylpyridin-2-yl)amine

https://huagongshe.com/reaction/1716529

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Amino-4-methylpyridineHCID 1533—
Reactant2,6-DibromopyridineHCID 12274—
ReactantBinap, (A+-)-HCID 634876—
ReactantSodium t-butoxideHCID 23676156—
Catalystpalladium(II) acetateHCID 167845—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
Product(6-Bromopyridin-2-yl)-(4-methylpyridin-2-yl)amineHCID 58706668110.5%

Reaction Conditions

Temperature80 °C

Reaction Steps

A suspension of 2,6-dibromopyridine (12.5 g), 2-amino-4-picoline (32.8 g, 139 mmol), palladium acetate (2.59 g, 11.6 mmol), rac-2,2′-bis(diphenylphosphino)-1,1′-binaphthyl (8.64 g, 13.9 mmol), sodium tert-butoxide (13.3 g, 139 mmol) in toluene (200 ml) was heated and stirred in an Ar stream at 80° C. for 12 hours. Water was added to the reaction solution and the solution was extracted with ethyl acetate. After the organic layer was washed with a saturated brine and dried over anhydrous magnesium sulfate, the residue obtained by vacuum concentration was purified by flash chromatography on silica gel (n-hexane:ethyl acetate=3:1) and subsequently washed with isopropyl ether and the title compound (15.4 g, 51%) was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07803801B2
Source datasetuspto-grants-2010_09
ORD IDord-93e7b71752174768b691c11d26e98431
Source noteuspto-grants-2010_09