Ethyl isocyanate → HCID 60969782, Verbindung
Reaktionsgleichung
[NH2:1][C:2]1[CH:3]=[C:4]([S:9]([NH2:12])(=[O:11])=[O:10])[CH:5]=[CH:6][C:7]=1[Cl:8].[CH2:13]([N:15]=[C:16]=[O:17])[CH3:14]>O1CCCC1>[Cl:8][C:7]1[CH:6]=[CH:5][C:4]([S:9]([NH2:12])(=[O:11])=[O:10])=[CH:3][C:2]=1[NH:1][C:16]([NH:15][CH2:13][CH3:14])=[O:17]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
To 3-amino-4-chlorobenzenesulfonamide (420 mg) in tetrahydrofuran (2 ml) solution, ethylisocyanate (180 μl) was added and the mixture was stirred under heating and reflux for 15 hours. The reaction solution was concentrated, then the residue was recrystallized from chloroform/methanol to obtain the title compound as a crude product (550 mg).
Aufarbeitung
- temperatureunder heating
- temperaturereflux for 15 hours
- concentrationThe reaction solution was concentrated
- customthe residue was recrystallized from chloroform/methanol
Quellen und Nachweise
- ORD-Eintrag
- ord-cef6fe54b21f41878aeb11ea3250ed2f
- Quelldatensatz
- uspto-grants-2011_11
- Patentnummer
- US08049006B2
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