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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 450390Erstellt: 26. Oktober 2026

Diisopropylethylamine → 2-Chloro-N-(5-methyl-1H-pyrazol-3-yl)-5-nitro-N-(tetrahydro-2H-pyran-4-yl)pyrimidine-4,6-diamine

https://huagongshe.com/reaction/450390

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiisopropylethylamineHCID 81531—
Edukt1H-Pyrazol-3-amine, 5-methyl-HCID 93146—
Edukt2,4,6-Trichloro-5-nitropyrimidineHCID 4297843—
Edukt2H-pyran-4-amineHCID 17791271—
LösungsmittelEthanolHCID 702—
LösungsmittelWaterHCID 962—
LösungsmittelEthyl AcetateHCID 8857—
Produkt2-Chloro-N-(5-methyl-1H-pyrazol-3-yl)-5-nitro-N-(tetrahydro-2H-pyran-4-yl)pyrimidine-4,6-diamineHCID 86649284—

Reaktionsschritte

To a solution of 2,4,6-trichloro-5-nitro pyrimidine (Intermediate 37, 1 g, 4.4 mmol) in EtOH at −50° C. were added 5-methyl-1H-pyrazol-3-amine (255 mg) and DIPEA (1.6 ml) drop-wise. The resulting mixture was stirred at this temperature for 5 minutes whereupon 4-amino pyran (300 mg) was added. The resulting mixture was allowed to warm to ambient temperature for 4 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 Gilson (MeCN/H2O, 5%→95%, 15 minutes) gave the title compound (120 mg). LCMS: 354 [M+1].

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08486966B2
Quelldatensatzuspto-grants-2013_07
ORD IDord-0cac8eba3950473ca5dbaaedd86949aa
Quellennotizuspto-grants-2013_07