Methanol → Methyl 1-(2-hydroxyethyl)-1H-benzimidazole-7-carboxylate

Temperatur

100 °C

Suspension of methyl 2-[(2-hydroxyethyl)amino]-3-nitrobenzoate (3.06 g, 12.7 mmol) in methanol (130 mL) was hydrogenated at atmospheric pressure over 10% palladium on activated charcoal for 10 min. The mixture was filtered through a pad of Celite and the solvent was removed in vacuum. The residue was dissolved in formic acid (60 mL) and heated at 100° C. for 45 min and then kept at ambient temperature overnight. Excess of the formic acid was removed under reduced pressure. The residue was dissolved in methanol (100 mL) and treated with concentrated ammonia in methanol (20 mL) for 50 min followed by evaporation of the volatiles. Purification by column chromatography on silica using dichloromethane in methanol 95:5 afforded methyl 1-(2-hydroxyethyl)-1H-benzimidazole-7-carboxylate, 2.31 g (83%). %). MS (ESI) m/z 221 [M+H]. 1H NMR (400 MHz, CD3OD) δ ppm 3.78 (t, J=5.05 Hz, 2H), 3.96 (s, 3H), 4.70 (t, J=5.05 Hz, 2H), 7.33 (t, J=7.83 Hz, 1H), 7.84-7.91 (m, 2H), 8.20 (s, 1H).

1. filtrationThe mixture was filtered through a pad of Celite
2. customthe solvent was removed in vacuum
3. dissolutionThe residue was dissolved in formic acid (60 mL)
4. customExcess of the formic acid was removed under reduced pressure
5. dissolutionThe residue was dissolved in methanol (100 mL)
6. additiontreated with concentrated ammonia in methanol (20 mL) for 50 min
7. customfollowed by evaporation of the volatiles
8. customPurification by column chromatography on silica

ORD-Eintrag

ord-86af66fcc24e40118243bc78edb3c58c

Quelldatensatz

uspto-grants-2010_01

DOI

10.6084/m9.figshare.5104873.v1

Patentnummer

US07645784B2