反应详情

A solution of diethyl azodicarboxylate (1.15 ml, 7.3 mmol) in methylene chloride (2 ml) was added in portions to a suspension of 4-chloro-6-cyano-7-hydroxyquinoline (1 g, 4.9 mmol), (prepared as described for the starting material in Example 1), 2-(1,2,3-triazol-1-yl)-ethan-1-ol (663 mg, 5.9 mmol), (J. Antib. 1993, 46, 177), and triphenylphosphine (1.92 g, 7.3 mmol) in methylene chloride (150 ml). After stirring for 10 minutes at ambient temperature, triphenylphosphine (256 mg, 0.98 mmol) was added followed by diethyl azodicarboxylate (154 μl, 0.98 mmol). The reaction mixture was stirred for 30 minutes and the volatiles were removed under vacuum and the residue was purified by column chromatography eluting with methylene chloride/ethyl acetate/methanol (45/50/5). The fractions containing the expected product were combined and evaporated under vacuum. The residue was triturated with ether, collected by filtration, washed with ether and dried under vacuum to give 4-chloro-6-cyano-7-(2-(1,2,3-triazol-1-yl)ethoxy)quinoline (470 mg, 32%).

1. custom(prepared
2. stirringThe reaction mixture was stirred for 30 minutes
3. customthe volatiles were removed under vacuum
4. customthe residue was purified by column chromatography
5. washeluting with methylene chloride/ethyl acetate/methanol (45/50/5)
6. additionThe fractions containing the expected product
7. customevaporated under vacuum
8. customThe residue was triturated with ether
9. filtrationcollected by filtration
10. washwashed with ether
11. customdried under vacuum