Hydrochloric Acid → N-(4-Formyl-2-pyrimidinyl)acetamide

HRID 233542Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 233542
C[O-].[Na+].C(O[O:8][CH:9](OC)[C:10]1[CH:15]=[CH:14][N:13]=[C:12]([NH:16][C:17](=[O:19])[CH3:18])[N:11]=1)(=O)C.Cl>CO>[C:17]([NH:16][C:12]1[N:11]=[C:10]([CH:9]=[O:8])[CH:15]=[CH:14][N:13]=1)(=[O:19])[CH3:18]

Komponenten

5

Versuchsvorschrift

Sodium methoxide (0.056 g, 1.0 mmol) was added to a solution of 2-acetamidopyrimidine-4-carboxaldehyde monomethyl monoacetoxy acetal (5.0 g, 21 mmol) in MeOH (25 mL) at ambient temperature. After stirring at this temperature for 3 h, the reaction mixture was neutralized by addition of 3N HCl. The resulting solution was concentrated and the residue was treated with CH2Cl2. Remaining solids were removed by filtration and the solvent was evaporated to afford the title compound as a yellow solid; yield 3.2 g (92%).

Aufarbeitung

  1. concentrationThe resulting solution was concentrated
  2. additionthe residue was treated with CH2Cl2
  3. customwere removed by filtration
  4. customthe solvent was evaporated

Quellen und Nachweise

ORD-Eintrag
ord-79fcad1f2e4446a2b19c103c55e8293e
Quelldatensatz
uspto-grants-1997_01
Patentnummer
US05593991

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