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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2409099Erstellt: 26. Oktober 2026

Dimethylformamide → 2-(1,5-dimethyl-1H-pyrazol-4-ylamino)-4-(methylamino)pyrimidine-5-carbonitrile

https://huagongshe.com/reaction/2409099

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethylformamideHCID 6228—
Edukt5-bromo-N2-(1,5-dimethyl-1H-pyrazol-4-yl)-N4-methylpyrimidine-2,4-diamineHCID 69081933—
KatalysatorZinc cyanide (Zn(CN)2)HCID 11186—
KatalysatorFerrocene-1,1'-bis-(diphenylphosphine)HCID 635956—
KatalysatorBis(dibenzylideneacetone)palladiumHCID 9811564—
Produkt2-(1,5-dimethyl-1H-pyrazol-4-ylamino)-4-(methylamino)pyrimidine-5-carbonitrileHCID 6909310725%

Reaktionsbedingungen

Temperatur105 °C

Reaktionsschritte

To a mixture of 5-bromo-N2-(1,5-dimethyl-1H-pyrazol-4-yl)-N4-methylpyrimidine-2,4-diamine (95 mg, 0.32 mmol), zinc cyanide (70 mg, 0.60 mmol), Pd2(dba)3 (11 mg, 0.012 mmol), DPPF (13 mg, 0.023 mmol) was added DMF (3.5 mL). The reaction was then heated in a sealed tube at 105° C. for 18 h. The reaction mixture was filtered and concentrated. The crude product was purified by reverse phase HPLC to give 2-(1,5-dimethyl-1H-pyrazol-4-ylamino)-4-(methylamino)pyrimidine-5-carbonitrile (19 mg, 25%). LCMS (Method A): [MH+]=244.1 at 2.53 min. 1H-NMR (DMSO): δ 8.96 (m, 1H), 8.21 (m, 1H), 7.49 (m, 2H), 3.69 (s, 3H), 2.84 (m, 3H), 2.14 (m, 3H). K1=0.025.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08815882B2
Quelldatensatzuspto-grants-2014_08
ORD IDord-2f32becfc4ba46c2be66b15cd07c4a73
Quellennotizuspto-grants-2014_08