Propyl mercaptan → 1,3-Dimethyl-2,4-dioxo-6-(propylthio)-1,2,3,4-tetrahydropyrimidine-5-carbaldehyde

HRID 42695Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 42695
[CH2:1]([SH:4])[CH2:2][CH3:3].[H-].[Na+].Cl[C:8]1[N:13]([CH3:14])[C:12](=[O:15])[N:11]([CH3:16])[C:10](=[O:17])[C:9]=1[CH:18]=[O:19]>O1CCOCC1>[CH3:14][N:13]1[C:8]([S:4][CH2:1][CH2:2][CH3:3])=[C:9]([CH:18]=[O:19])[C:10](=[O:17])[N:11]([CH3:16])[C:12]1=[O:15]

Komponenten

5

Versuchsvorschrift

To a stirred solution of propane-1-thiol (2.30 mmol) in dry 1,4-dioxane (4 ml), NaH (2.30 mmol) was added under argon. To the mixture, a solution of 6-chloro-1,3-dimethyl-2,4-dioxo-1,2,3,4-tetrahydropyrimidine-5-carbaldehyde (2 mmol) in dry 1,4-dioxane (8 ml) was added at 5-8° C. in one portion. The mixture was stirred at room temperature until the starting material was consumed (monitored by TLC). Then the mixture was poured onto ice water (50 ml) and the aqueous phase was extracted with ethyl acetate (3×30 ml). The combined organic phases were washed with water and dried over anhydrous MgSO4. The solvent was evaporated in vacuo and the crude product was purified by column chromatography with a mixture of n-hexane:ethyl acetate (1:1) as the eluent.

Aufarbeitung

  1. customwas consumed (monitored by TLC)
  2. additionThen the mixture was poured onto ice water (50 ml)
  3. extractionthe aqueous phase was extracted with ethyl acetate (3×30 ml)
  4. washThe combined organic phases were washed with water
  5. dry with materialdried over anhydrous MgSO4
  6. customThe solvent was evaporated in vacuo
  7. customthe crude product was purified by column chromatography with a mixture of n-hexane:ethyl acetate (1:1) as the eluent

Quellen und Nachweise

ORD-Eintrag
ord-36c7cc926e514e7ea932e77118df6091
Quelldatensatz
uspto-grants-2013_09
Patentnummer
US08536210B2

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