Formic Acid → 4-BROMO-6-FLUORO-1H-BENZO[D]IMIDAZOLE
Reaktionsgleichung
[Br:1][C:2]1[CH:7]=[C:6]([F:8])[CH:5]=[C:4]([NH2:9])[C:3]=1[NH2:10].[CH:11](O)=O>>[Br:1][C:2]1[C:3]2[N:10]=[CH:11][NH:9][C:4]=2[CH:5]=[C:6]([F:8])[CH:7]=1Komponenten
3
Reaktionsbedingungen
- Temperatur
- 110 °C
Versuchsvorschrift
A mixture of 3-bromo-5-fluorobenzene-1,2-diamine (10.1 g, 49 mmol) in formic acid (20 mL) was heated at 110° C. overnight. The reaction mixture was concentrated, and to the residue was added MeOH (5 mL) to form a precipitate. The precipitate was filtered and washed with MeOH (2 mL) to afford 4-bromo-6-fluoro-1H-benzo[d]imidazole as a yellow solid (10 g, yield, 73%). MS (ESI): m/z=215 [M+1]+.
Aufarbeitung
- concentrationThe reaction mixture was concentrated
- additionto the residue was added MeOH (5 mL)
- customto form a precipitate
- filtrationThe precipitate was filtered
- washwashed with MeOH (2 mL)
- customto afford
Quellen und Nachweise
- ORD-Eintrag
- ord-0aca8d3d4229468da5e32b77f0b06e5a
- Quelldatensatz
- uspto-grants-2014_01
- Patentnummer
- US08637537B2
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