Ethyl isocyanate → 1-(4-Bromopyridin-2-yl)-3-ethylurea
Reaktionsgleichung
[Br:1][C:2]1[CH:7]=[CH:6][N:5]=[C:4]([NH2:8])[CH:3]=1.[N:9]([CH2:12][CH3:13])=[C:10]=[O:11]>C(Cl)(Cl)Cl>[Br:1][C:2]1[CH:7]=[CH:6][N:5]=[C:4]([NH:8][C:10]([NH:9][CH2:12][CH3:13])=[O:11])[CH:3]=1Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- 110 °C
Versuchsvorschrift
To a mixture of 4-bromopyridin-2-amine (2 g, 11.56 mmol) in chloroform (10 mL), isocyanatoethane (0.913 mL, 11.56 mmol) was added, and the resulting reaction mixture was heated at 110° C. for 2 h. The reaction mixture was concentrated under reduced pressure and triturated with acetonitrile, then collected by filtered to give the title compound as a white solid (2.15 g).
Aufarbeitung
- additionwas added
- customthe resulting reaction mixture
- concentrationThe reaction mixture was concentrated under reduced pressure
- customtriturated with acetonitrile
- customcollected
- filtrationby filtered
Quellen und Nachweise
- ORD-Eintrag
- ord-45a5880b52564e1bb2cf746037031595
- Quelldatensatz
- uspto-grants-2010_03
- Patentnummer
- US07674801B2
Notizen zur Reaktion
Wird geladen…