Hydrazine → HCID 178446231, Verbindung
Reaktionsgleichung
CS[C:3]1[C:4]2[NH:5][C:6]([C:18]([F:21])([F:20])[F:19])=[N:7][C:8]=2[N:9]([CH2:13][CH2:14][CH2:15][CH2:16][CH3:17])[C:10](=[O:12])[N:11]=1.[NH2:22][NH2:23]>O>[CH2:13]([N:9]1[C:8]2[N:7]=[C:6]([C:18]([F:21])([F:20])[F:19])[NH:5][C:4]=2/[C:3](=[N:22]\[NH2:23])/[NH:11][C:10]1=[O:12])[CH2:14][CH2:15][CH2:16][CH3:17]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- 100 °C
Versuchsvorschrift
A mixture of 6-(methylthio)-3-pentyl-8-(trifluoromethyl)-3,7-dihydro-2H-purin-2-one (0.15 g, 0.23 mmol) and hydrazine (0.80 mL, 25 mmol) in water (0.80 mL) was heated at 100° C. for 1 h. The solution was concentrated under reduced pressure and azeotropically treated with toluene twice. The resulting residue was used for next step without purification. LCMS calculated for C11H16F3N6O (M+H): 305.1. found: 305.1.
Aufarbeitung
- concentrationThe solution was concentrated under reduced pressure
- additionazeotropically treated with toluene twice
- customThe resulting residue was used for next step without purification
Quellen und Nachweise
- ORD-Eintrag
- ord-dbf37206e9304c20ad3459f889b0229f
- Quelldatensatz
- uspto-grants-2011_01
- Patentnummer
- US07863285B2
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