反应详情

n-Butyllithium (3.55 cm3 of a 1.55M solution in hexane) was added dropwise to a stirred solution of 1-methyl-benzimidazole (0.6 g) in tetrahydrofuran (THF) (10 cm3) at -50° under nitrogen. After 1 hour a solution of anhydrous zinc chloride (1.5 g) in THF (10 cm3) was added and the mixture allowed to warm to room temperature. 2-Methoxy-6-bromo-8-methylquinoline (1.25 g) and tetrakis (triphenylphosphine)palladium (O) (0.05 g) were added and the mixture heated under reflux for 4 hours. Saturated ammonium chloride solution (10 cm3) was added to the cooled mixture, followed by a solution of ethylenediamine tetraacetic acid disodium salt (12.0 g) in water (200 cm3). Ethyl acetate (200 cm3 and methanol (20 cm3) were added and the phase separated. The aqueous layer was further extracted with methanol:dichloromethane; 1:20 by volume (2×200 cm3) and the combined and dried (MgSO4) organic extracts were evaporated in vacuo to afford a solid which was chromatographed on silica (Merck "MK 60.9385" [Trade Mark]) eluting with methanol:dichloromethane, 1:100 by volume. Combination and evaporation of appropriate fractions gave the title compound (1.05 g) which was characterised spectroscopically and used in Example 4 without further purification.

1. temperaturethe mixture heated
2. temperatureunder reflux for 4 hours
3. customthe phase separated
4. extractionThe aqueous layer was further extracted with methanol
5. dry with materialdried (MgSO4) organic extracts
6. customwere evaporated in vacuo
7. customto afford a solid which
8. customwas chromatographed on silica (Merck "MK 60.9385" [Trade Mark])
9. washeluting with methanol
10. customCombination and evaporation of appropriate fractions