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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1255884Erstellt: 27. Oktober 2026

Triethylamine → [1-(4-Methoxyphenyl)ethyl]-2-methylpteridin-4-yl-amine

https://huagongshe.com/reaction/1255884

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
Edukt1,4-Dioxane-2,3-diolHCID 96170—
Edukt1-(4-Methoxyphenyl)ethanamineHCID 238181—
Edukt6-Chloro-2-methylpyrimidine-4,5-diamineHCID 594145—
LösungsmittelEthanolHCID 702—
LösungsmittelEthyl acetate hexaneHCID 21226206—
Produkt[1-(4-Methoxyphenyl)ethyl]-2-methylpteridin-4-yl-amineHCID 5817422821,3%

Reaktionsbedingungen

Temperatur25 °C

Reaktionsschritte

A mixture of 6-chloro-4,5-diamino-2-methylpyrimidine (317 mg, 2.0 mmol) and 1,4-dioxane-2,3-diol (240 mg, 2.0 mmol) in EtOH (15 mL) was stirred at 25° C. for 1 h. TLC analysis (1:1 hexane/EtOAc on SiO2) indicated complete consumption of starting material. 1-(4-Methoxyphenyl)-ethylamine (332 mg, 2.2 mmol) and triethylamine (Et3N, 0.3 mL, 2.2 mmol) were added, and the reaction was stirred overnight. The majority of solvent was removed in vacuo and the residue was partitioned between EtOAc and H2O. The organic layer was concentrated in vacuo to leave a brown residue that was purified by column chromatography over SiO2, eluting with 2:1 EtOAc/hexane, then 100% EtOAc to afford [1-(4-methoxyphenyl)ethyl]-2-methylpteridin-4-yl-amine (126 mg) as a brown oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08461164B2
Quelldatensatzuspto-grants-2013_06
ORD IDord-2d652c990f454b36b30dbadce40fb6c8
Quellennotizuspto-grants-2013_06