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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1274997Erstellt: 27. Oktober 2026

2-Chloro-N,N-dimethylpyrimidin-4-amine → N4,N4-dimethyl-N2-[1-(2-phenylethyl)-4-piperidinyl]-2,4-pyrimidinediamine

https://huagongshe.com/reaction/1274997

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-Chloro-N,N-dimethylpyrimidin-4-amineHCID 95975—
Edukt1-(2-Phenylethyl)piperidin-4-amineHCID 10728788—
LösungsmittelWaterHCID 962—
ProduktN4,N4-dimethyl-N2-[1-(2-phenylethyl)-4-piperidinyl]-2,4-pyrimidinediamineHCID 5392113128,4%

Reaktionsbedingungen

Temperatur120 °C

Reaktionsschritte

A mixture of 1-(2-phenylethyl)-4-piperidinamine (8.17 g) and 2-chloro-N,N-dimethyl-4-pyrimidinamine (6.3 g) was stirred for 20 hours at 120° C. The reaction mixture was diluted with water and extracted with CH2Cl2. The organic layer was washed with water, dried, filtered and the solvent evaporated. The residue was purified by column chromatography over silica gel (eluent: CH2Cl2 /CH3OH(NH3) 96/4). The pure fractions were collected and the solvent evaporated. The residue was crystallized from CH3CN. The precipitate was filtered off and dried, yielding 3.69 g (28.4%) of N4,N4 -dimethyl-N2 -[1-(2-phenylethyl)-4-piperidinyl]-2,4-pyrimidinediamine (comp. 11).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06159982
Quelldatensatzuspto-grants-2000_12
ORD IDord-af6cd92b99fd43cf8bb49c0d311e7a2d
Quellennotizuspto-grants-2000_12