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HRID 267497Erstellt: 24. Oktober 2026

Dimethyl Sulfoxide → 2,6-Di(methylamino)-3,5-dinitropyridine

https://huagongshe.com/reaction/267497

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethyl SulfoxideHCID 679—
EduktMethylamineHCID 6329—
Edukt3,5-Dinitropyridine-2,6-diamineHCID 542959—
LösungsmittelMethanolHCID 887—
LösungsmittelDimethylacetamideHCID 31374—
Produkt2,6-Di(methylamino)-3,5-dinitropyridineHCID 21554890—

Reaktionsbedingungen

Temperatur70 °C

Reaktionsschritte

To a solution of 2,6-diamino-3,5-dinitropyridine (25.0 g, 0.125 mole) and 225 ml dimethylsulfoxide in a 500 ml Parr bottle was added a solution of methylamine (20 g, 0.65 mole) in 75 ml N,N-dimethylacetamide (DMAc). The reaction was shaken for 4 hours at ambient temperatures and then heated 20 hours at 70°C. Upon cooling, the heterogeneous mixture was diluted with 100 ml methanol, filtered, washed with 200 ml DMAc-methanol (lv/lv), twice with methanol and dried. 2,6-Di(methylamino)-3,5-dinitropyridine, m.p. 323°-325°C (dec.) was obtained as a golden yellow solid (25.0 g, 93% yield). This product, unlike 2,6-diamino-3,5-dinitropyridine, is essentially insoluble in dimethylsulfoxide and 85% H3PO4. Anal. Calcd. for C7H9N5O4 : C, 37.0; H, 4.0; N, 30.8. Found: C, 37.2; H, 3.8; N, 31.0.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS03943125
Quelldatensatzuspto-grants-1976_03
ORD IDord-c53048a57f57486b8ed6b1a221694a0b
Quellennotizuspto-grants-1976_03