Hydrochloric Acid → (4-Methoxy-6-Methyl-2-pyriMidinyl)thiourea, 97+%
Reaktionsgleichung
[CH3:1][O:2][C:3]1[CH:8]=[C:7]([CH3:9])[N:6]=[C:5]([NH:10][C:11]([NH:13]NC(=O)C2C=CC=CC=2)=[S:12])[N:4]=1.[OH-].[Na+].Cl>>[CH3:1][O:2][C:3]1[CH:8]=[C:7]([CH3:9])[N:6]=[C:5]([NH:10][C:11]([NH2:13])=[S:12])[N:4]=1Komponenten
4
Versuchsvorschrift
A mixture of 25 g of the compound from Example 3 and 55 ml of 10% aqueous sodium hydroxide was heated on the steam bath for 30 minutes, cooled, neutralized with aqueous HCl to pH 8, filtered, washed with water, dried by suction, and washed with ether to afford 16 g of the title compound, m.p. 220° d.
Aufarbeitung
- temperaturewas heated on the steam bath for 30 minutes
- temperaturecooled
- filtrationfiltered
- washwashed with water
- customdried by suction
- washwashed with ether
Quellen und Nachweise
- ORD-Eintrag
- ord-a40805c7071b481f815b33baed5200e6
- Quelldatensatz
- uspto-grants-1987_08
- Patentnummer
- US04689070
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