反应详情

Methyl 6-acetyl-4-chloro-7-hydroxy-8-propyl-quinoline-2-carboxylate (1.0 g) and diethyl oxalate (3.7 mls) in dry dimethylformamide (25 mls) was added to ether washed 50% sodium hydride (0.65 g) suspended in dry dimethyl formamide (25 mls) under nitrogen with stirring. The reaction mixture was stirred for 5 hours at room temperature, poured into ethyl acetate, aqueous acetic acid was added and the organic layer separated, washed well with water and dried. The solvent was evaporated, the residue dissolved in dry dioxan (100 mls) and dry hydrogen chloride gas passed through the solution for 20 minutes. The reaction mixture was poured into ethyl acetate, washed well with water, saturated sodium bicarbonate solution then water again and dried. The solvent was evaporated and the residue triturated with 40-60 petroleum ether to give 0.9 g of the title product. The structure was confirmed by NMR and MS evidence. The product was converted to the free acid and the disodium salt using the techniques of Example 1(b) and (c).

1. washwashed 50% sodium hydride (0.65 g)
2. stirringThe reaction mixture was stirred for 5 hours at room temperature
3. additionpoured into ethyl acetate, aqueous acetic acid
4. additionwas added
5. customthe organic layer separated
6. washwashed well with water
7. customdried
8. customThe solvent was evaporated
9. dissolutionthe residue dissolved in dry dioxan (100 mls)
10. additionThe reaction mixture was poured into ethyl acetate
11. washwashed well with water, saturated sodium bicarbonate solution
12. dry with materialwater again and dried
13. customThe solvent was evaporated
14. customthe residue triturated with 40-60 petroleum ether