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HRID 1814902Erstellt: 25. Oktober 2026

2,4,6-Trimethylaniline → 5-bromo-2-chloro-N-(2,4,6-trimethylphenyl)-4-pyrimidinamine

https://huagongshe.com/reaction/1814902

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2,4,6-TrimethylanilineHCID 6913—
EduktDiisopropylethylamineHCID 81531—
Edukt5-Bromo-2,4-dichloropyrimidineHCID 289973—
Lösungsmittel1,4-DioxaneHCID 31275—
Produkt5-bromo-2-chloro-N-(2,4,6-trimethylphenyl)-4-pyrimidinamineHCID 2217008665%
Produkt5-bromo4-chloro-N-(2,4,6-trimethylphenyl)-2-pyrimidinamineHCID 2217010224%

Reaktionsschritte

Reaction under argon atmosphere. A solution of 2,4,6-trimethylbenzenamine (0.00461 mol) in 1,4-dioxane (5 ml) was added to a solution of 5-bromo-2,4-dichloropyrimidine (0.00439 mol) in 1,4-dioxane (5 ml). N,N-bis(1-methylethyl)ethanamine (0.00548 mol) was added. The reaction mixture was stirred and refluxed for 20 hours. The solvent was evaporated. The residue was dissolved in ethyl acetate, washed with a saturated aqueous sodium bicarbonate solution, water and brine, dried with sodium sulfate, filtered, and the solvent was evaporated. The residue was purified by column chromatography over silica gel (eluent: 1:5, 1:2 and 1:1 CH2Cl2: hexane). Two pure fraction groups were collected and their solvent was evaporated, yielding 0.35 g (24%) of 5-bromo-4-chloro-N-(2,4,6-trimethylphenyl)-2-pyrimidinamine (interm. 1) and 0.93 g (65%) of 5-bromo-2-chloro-N-(2,4,6-trimethylphenyl)-4-pyrimidinamine (interm. 2).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06878717B2
Quelldatensatzuspto-grants-2005_04
ORD IDord-b186d8c8816945a3972f27eb5457bcd1
Quellennotizuspto-grants-2005_04