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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 450392Erstellt: 25. Oktober 2026

Morpholine → N-(5-Methyl-1H-pyrazol-3-yl)-2-(methylthio)-6-morpholin-4-yl-5-nitropyrimidin-4-amine

https://huagongshe.com/reaction/450392

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMorpholineHCID 8083—
EduktDiisopropylethylamineHCID 81531—
Edukt1H-Pyrazol-3-amine, 5-methyl-HCID 93146—
Edukt4,6-Dichloro-2-(methylthio)-5-nitropyrimidineHCID 11345458—
LösungsmittelWaterHCID 962—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelEthyl AcetateHCID 8857—
ProduktN-(5-Methyl-1H-pyrazol-3-yl)-2-(methylthio)-6-morpholin-4-yl-5-nitropyrimidin-4-amineHCID 68734536—

Reaktionsschritte

To a solution of 4,6-dichloro-2-(methylthio)-5-nitropyrimidine (Intermediate 56, 820 mg) in THF at 0° C. were added 5-methyl-1H-pyrazol-3-amine (350 mg) and DIPEA (1.6 ml) drop-wise. The resulting mixture was stirred at this temperature for 3 hours whereupon morpholine (1 ml) was added. The resulting mixture was allowed to warm to ambient temperature over 10 hours. The mixture was diluted with H2O and EtOAc and the aqueous layer was extracted with EtOAc. The combined organic layers were washed with brine, saturated NaHCO3 (aq) solution, dried and evaporation of the volatiles under reduced pressure gave a colored residue. Purification by column chromatography (50% EtOAc/hexanes) gave the title compound (820 mg). LCMS: 352 [M+1].

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08486966B2
Quelldatensatzuspto-grants-2013_07
ORD IDord-0e93f9d296b14d52880e09c304f1e6b5
Quellennotizuspto-grants-2013_07