Hydrochloric Acid → 2-Aminopyrimidine-4-carbaldehyde

HRID 605862Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 605862
C[O:2][CH:3](OC)[C:4]1[CH:9]=[CH:8][N:7]=[C:6]([NH2:10])[N:5]=1.Cl.C([O-])(O)=O.[Na+]>CCOC(C)=O>[NH2:10][C:6]1[N:5]=[C:4]([CH:3]=[O:2])[CH:9]=[CH:8][N:7]=1

Komponenten

5

Edukt 3

HCID 313Hydrochloric AcidHCID 516892Sodium BicarbonateHCID 49130324-(dimethoxymethyl)pyrimidin-2-amine

Produkt 1

HCID 178323462-Aminopyrimidine-4-carbaldehydeAusbeute 37,4 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8857Ethyl AcetateLösungsmittel

Versuchsvorschrift

A solution of 2.5 g (15 mmol, 1.0 eq.) 2-aminopyrimidine-4-carboxaldehyde dimethylacetal in 16 ml (45 mmol, 3 eq.) of 3M HCl was heated at 48° C. for 14 h. The mixture was cooled to r.t. and layered with 50 mL of EtOAc. The aqueous layer was neutralized with NaHCO3 and then extracted with EtOAc (5×50 ml). The combined extracts were dried (Na2SO4) and concentrated in vacuo afford 0.69 g (37%) of 2-aminopyrimidine-4-carboxaldehyde.

Aufarbeitung

  1. extractionextracted with EtOAc (5×50 ml)
  2. dry with materialThe combined extracts were dried (Na2SO4)
  3. concentrationconcentrated in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-f4aa597910cc4dcab949b870cd5bf2ef
Quelldatensatz
uspto-grants-2011_03
Patentnummer
US07915268B2

Notizen zur Reaktion

Wird geladen…