Water → Benzimidazole

2-Amino-5-(2′,2′-dimethylpropionyl)benzimidazole: To a flask containing 60 mL H2O was added 11.32 mL of a 5.0 M solution of cyanogen bromide in CH3CN followed by the addition of 10.71 g 4-(2′,2′-dimethylpropionyl)-1,2-aminobenzene (51.5 mmol, prepared above in step (b), 1.0 equiv) in 60 mL EtOH over 30 min via addition funnel. After stirring for 20 h the solution was concentrated under reduced pressure to remove the EtOH. The resulting aqueous solution was washed (2×EtOAc), and the EtOAc fractions were back extracted 2×H2O. The combined aqueous layers were made basic with sat. NaHCO3, and then extracted (3×EtOAc). The organic layer was then washed (1×brine), dried (MgSO4), and concentrated under reduced pressure to give the product benzimidazole as a brown solid (8.59 g, 36.8 mmol): 1H NMR (DMSO-d6, 400 MHz) δ 7.04 (d, J=8.3 Hz, 1H), 6.79 (d, J=2.2 Hz, 1H), 6.53 (dd, J=2.2, 8.3 Hz, 1H), 6.31 (broad s, 2H), 1.28 (s, 9H).

1. concentrationwas concentrated under reduced pressure
2. customto remove the EtOH
3. washThe resulting aqueous solution was washed (2×EtOAc)
4. extractionthe EtOAc fractions were back extracted 2×H2O
5. extractionextracted (3×EtOAc)
6. washThe organic layer was then washed (1×brine)
7. dry with materialdried (MgSO4)
8. concentrationconcentrated under reduced pressure

ORD record

ord-e675a9450a5b444699fbd73ab1381125

Source dataset

uspto-grants-2009_12

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US07635774B2