Methylthiouracil → HCID 135559187, Verbindung
Reaktionsgleichung
[Cl-].Cl[CH2:3][C:4]1[CH:9]=[CH:8][C:7]([CH2:10][CH3:11])=[CH:6][NH+:5]=1.[CH3:12][C:13]1[NH:20][C:18](=[S:19])[NH:17][C:15](=[O:16])[CH:14]=1>>[CH2:10]([C:7]1[CH:8]=[CH:9][C:4]([CH2:3][S:19][C:18]2[NH:17][C:15](=[O:16])[CH:14]=[C:13]([CH3:12])[N:20]=2)=[N:5][CH:6]=1)[CH3:11]Komponenten
3
Versuchsvorschrift
The title compound is prepared from 2-chloromethyl-5-ethylpyridinium chloride (m.p.: 126°-128° C.) and 6-methyl-2-thiouracyl by using the process described in Example 12. After recrystallization from ethanol the title compound is obtained as a white crystalline product in a yield of 51%, m.p.: 127°-128° C.
Aufarbeitung
- customAfter recrystallization from ethanol the title compound
- customis obtained as a white crystalline product in a yield of 51%, m.p.: 127°-128° C.
Quellen und Nachweise
- ORD-Eintrag
- ord-7f9d900f3ea945f7acc0f0689b1dd4e1
- Quelldatensatz
- uspto-grants-1991_08
- Patentnummer
- US05037830
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