Hydrochloric Acid → 6-Nitropyrido[2,3-d]pyrimidine-2,4-diamine

HRID 1062570

Reaktionsgleichung

Reaktionsgleichung von HRID 1062570
[NH2:1][C:2]1[N:7]=[C:6]([NH2:8])[CH:5]=[C:4]([NH2:9])[N:3]=1.Cl.[N+:11]([CH:14]([CH:17]=O)[CH:15]=O)([O-:13])=[O:12]>C(O)C>[NH2:1][C:2]1[N:3]=[C:4]([NH2:9])[C:5]2[CH:17]=[C:14]([N+:11]([O-:13])=[O:12])[CH:15]=[N:8][C:6]=2[N:7]=1

Komponenten

5

Edukt 3

HCID 313Hydrochloric AcidHCID 138632,4,6-TriaminopyrimidineHCID 313475Nitromalonaldehyde

Produkt 1

HCID 110527766-Nitropyrido[2,3-d]pyrimidine-2,4-diamine

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 702EthanolLösungsmittel

Versuchsvorschrift

About 1 equivalent of 2,4,6-triamino pyrimidine was suspended in about 50 ml of refluxing absolute ethanol with stirring under an atmosphere of nitrogen. Concentrated HCl was added dropwise to effect solution and as soon as solution occurred, about 1.2 equivalents of nitromalonaldehyde was added all at once. Within 10 minutes, a thick reddish voluminous precipitate started forming. TLC analysis indicated the presence of a yellow spot corresponding to that of the desired product along with staring materials. The reaction mixture was stirred at reflux for 3.5 hours, immediately diluted with 30 ml of water, cooled and neutralized with concentrated NH4OH. The precipitate was collected on a funnel and was washed repeatedly with water to remove unreacted triamino pyrimidine to yield pure 2,4-diamino-6-nitropyrido[2,3-d]pyrimidine.

Aufarbeitung

  1. customa thick reddish voluminous precipitate started forming

Quellen und Nachweise

ORD-Eintrag
ord-eea00f97f15e4afbaa88e4962d6d317f
Quelldatensatz
uspto-grants-2005_11
Patentnummer
US06962920B2

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