反应详情

Molecular Sieves 4A (6 g) was added to a tert-butanol (45 ml) solution of the 2-bromo-5,6,7,8-tetrahydroimidazo[1,2-a]pyridine-7-carboxylic acid (3.1 g) obtained in (Example 2.7) <Step 3> and triethylamine (9.7 ml), and the obtained mixture was then stirred at room temperature for 30 minutes. Thereafter, diphenyl phosphate azide (3.8 ml) was added to the reaction solution, and the obtained mixture was stirred for 30 minutes and then at 110° C. for 4 hours. Thereafter, the reaction solution was filtered with Celite, and insoluble matters were then washed with ethyl acetate. After that, ethyl acetate (100 ml) was added to the filtrate, and the obtained mixture was successively washed with a saturated ammonium chloride aqueous solution (25 ml) three times, a saturated sodium hydrogen carbonate aqueous solution (25 ml) twice, and a saturated saline. Then, the solvent was distilled away under reduced pressure. Methylene chloride was added to the obtained residue, and precipitated white insoluble matters were then removed by suction filtration. The filtrate was concentrated under reduced pressure, and the obtained residue was then purified by silica gel column chromatography (silica gel:eluent; heptane:ethyl acetate=60:40-20:80), so as to obtain the title compound (1.3 g) in the form of a white solid.

1. stirringthe obtained mixture was stirred for 30 minutes
2. waitat 110° C. for 4 hours
3. filtrationThereafter, the reaction solution was filtered with Celite, and insoluble matters
4. washwere then washed with ethyl acetate
5. additionAfter that, ethyl acetate (100 ml) was added to the filtrate
6. washthe obtained mixture was successively washed with a saturated ammonium chloride aqueous solution (25 ml) three times
7. distillationThen, the solvent was distilled away under reduced pressure
8. additionMethylene chloride was added to the obtained residue
9. customprecipitated white insoluble matters
10. customwere then removed by suction filtration
11. concentrationThe filtrate was concentrated under reduced pressure
12. customthe obtained residue was then purified by silica gel column chromatography (silica gel:eluent; heptane:ethyl acetate=60:40-20:80)