Hydrochloric Acid → 4-PHENYL-1-PIPERAZINECARBOTHIOAMIDE
Reaktionsgleichung
[C:1]1([N:7]2[CH2:12][CH2:11][N:10]([C:13]([NH:15]C(=O)OCC)=[S:14])[CH2:9][CH2:8]2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.Cl.[OH-].[Na+]>>[C:1]1([N:7]2[CH2:8][CH2:9][N:10]([C:13](=[S:14])[NH2:15])[CH2:11][CH2:12]2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1Komponenten
4
Reaktionsbedingungen
- Temperatur
- 80 °C
Versuchsvorschrift
Ethyl (4-phenyl-1-piperazinyl)carbothioylcarbamate (13 g, 44 mmol) was added to conc. hydrochloric acid (44 mL) and the mixture was stirred at 80° C. for 2 h. The reaction mixture was made basic with 8N aqueous sodium hydroxide solution and the crystals were collected by filtration. The crystals were washed with water and dried to give the title compound (6.1 g, yield 63%).
Aufarbeitung
- filtrationthe crystals were collected by filtration
- washThe crystals were washed with water
- customdried
Quellen und Nachweise
- ORD-Eintrag
- ord-39c6e7e35fd646cc9aeb751855e24757
- Quelldatensatz
- uspto-grants-2005_11
- Patentnummer
- US06962933B1
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