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HRID 1038729Erstellt: 25. Oktober 2026

HCID 66669752, Verbindung → 1-(2,6-Dichloro-3,5-dimethoxy-phenyl)-3-{6-[4-(4-ethyl-piperazin-1-yl)-phenylamino]-pyrimidin-4-yl}-urea

https://huagongshe.com/reaction/1038729

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHCID 66669752HCID 66669752—
Edukt2,6-Dichloro-3,5-dimethoxyphenyl isocyanateHCID 86086993—
LösungsmittelN-methyl-2-pyrrolidoneHCID 13387—
Produkt1-(2,6-Dichloro-3,5-dimethoxy-phenyl)-3-{6-[4-(4-ethyl-piperazin-1-yl)-phenylamino]-pyrimidin-4-yl}-ureaHCID 57710314—

Reaktionsbedingungen

Temperatur70 °C

Reaktionsschritte

2,6-dichloro-3,5-dimethoxyphenylisocyanate (1.2 eq.) is added to a solution of N-[4-(4-ethyl-piperazin-1-yl)-phenyl]-pyrimidine-4,6-diamine (350 mg, 1.18 mmol) in NMP (2 ml), at 70° C. and under an argon atmosphere. The resulting mixture is stirred at 70° C. for 2 h, allowed to cool to RT and concentrated. The residue is diluted with DCM and a saturated aqueous solution of sodium bicarbonate. The aqueous layer is separated and extracted with DCM. The organic phase is washed with brine, dried (sodium sulfate), filtered and concentrated. Purification of the crude product by trituration in MeOH followed by silica gel column chromatography (DCM/MeOH+1% NH3aq, 97:3) affords the title compound as a white solid:

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08552002B2
Quelldatensatzuspto-grants-2013_10
ORD IDord-87dcb4c970bc4d7da086923456dfaf1b
Quellennotizuspto-grants-2013_10