Acetic Acid → 5,6-dimethyl-2-(methylsulfanyl)pyrimidin-4(1h)-one

HRID 63120

Reaktionsgleichung

Reaktionsgleichung von HRID 63120
[CH3:1][C:2]1[C:3](=[O:10])[NH:4][C:5](=[S:9])[NH:6][C:7]=1[CH3:8].[OH-].[Na+].CI.[C:15](O)(=O)C>O>[CH3:1][C:2]1[C:3](=[O:10])[NH:4][C:5]([S:9][CH3:15])=[N:6][C:7]=1[CH3:8]

Komponenten

6

Versuchsvorschrift

To a stirred solution of 5,6-dimethyl-2-thioxo-2,3-dihydropyrimidin-4(1H)-one (10.0 g, 64.0 mmol, Example 1, Step A) and sodium hydroxide (10.0 g, 260.0 mmol) in water (150 mL) at ambient temperature was added methyl iodide (15.0 g, 320.0 mmol), and the reaction mixture was stirred at ambient temperature overnight. Then the reaction mixture was acidified with acetic acid (50 mL), and the solid was collected by filtration and dried to afford 7.0 g (64%) of the titled compound as a white solid. 1H NMR (300 MHz, DMSO-d6) δ ppm 1.87 (s, 3H), 2.18 (s, 3H), 2.45 (s, 3H), 12.38 (bs, 1H).

Aufarbeitung

  1. filtrationthe solid was collected by filtration
  2. customdried

Quellen und Nachweise

ORD-Eintrag
ord-8b9970a145f54e7f8cdb43222681458b
Quelldatensatz
uspto-grants-2016_09
Patentnummer
US09447051B2

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