반응 #481898

반응 방정식

4-[3-(R,S)-hydroxy-3-(3-fluoro-6-methoxyquinolin-4-yl)propyl)piperidine-3-carboxylate dihydrochloride

potassium carbonate

potassium iodide

2-(2-bromoethylthio)thiophene

→

methyl (3RS,4RS)-4-[3-(R,S)-hydroxy-3-(3-fluoro-6-methoxyquinolin-4-yl)propyl]-1-[2-(2-thienylthio)ethyl]piperidine-3-carboxylate

용매

acetonitrile

DMF

acetonitrile

triethylamine

반응 조건

후처리

1. 1
   온도After cooling to about 20° C.
2. 2
   여과the reaction mixture was filtered on sintered glass
3. 3
   농축concentrated under reduced pressure (5 kPa)
4. 4
   기타The organic phase was separated
5. 5
   세척washed with twice 75-cm3 of a saturated aqueous sodium chloride solution
6. 6
   건조dried over magnesium sulfate
7. 7
   여과filtered
8. 8
   농축concentrated under reduced pressure (5 kPa) at a temperature in the region of 40° C
9. 9
   기타The residue obtained
10. 10
    기타was purified by chromatography, under a nitrogen pressure of 50 kPa
11. 11
    세척on a column of silica gel (particle size 20-45 μ; diameter 2 cm; height 40 cm), eluting with a mixture of cyclohexane-ethyl acetate (25/75 by volume)
12. 12
    기타collecting 50-cm3 fractions
13. 13
    농축Fractions 6 to 8 were concentrated

실험 절차

0.74-cm3 of triethylamine was added to a solution composed of 1.17 g of methyl (3RS, 4RS) 4-[3-(R,S)-hydroxy-3-(3-fluoro-6-methoxyquinolin-4-yl)propyl)piperidine-3-carboxylate dihydrochloride in 20-cm3 of acetonitrile and 10-cm3 of DMF, followed by 638 mg of 2-(2-bromoethylthio)thiophene in 10-cm3 of acetonitrile, 1 g of potassium carbonate and 431 mg of potassium iodide. The mixture was stirred for 15 hours at a temperature in the region of 65° C. under an inert atmosphere. After cooling to about 20° C., the reaction mixture was filtered on sintered glass. The filtrate was taken up in 100-cm3of acetonitrile and concentrated under reduced pressure (5 kPa). The residue was taken up in 200-cm3 of ethyl acetate and 100-cm3 of water. The organic phase was separated after settling out, washed with twice 75-cm3 of a saturated aqueous sodium chloride solution, dried over magnesium sulfate, filtered, and concentrated under reduced pressure (5 kPa) at a temperature in the region of 40° C. The residue obtained was purified by chromatography, under a nitrogen pressure of 50 kPa, on a column of silica gel (particle size 20-45 μ; diameter 2 cm; height 40 cm), eluting with a mixture of cyclohexane-ethyl acetate (25/75 by volume) and collecting 50-cm3 fractions. Fractions 6 to 8 were concentrated. 630 mg of methyl (3RS,4RS)-4-[3-(R,S)-hydroxy-3-(3-fluoro-6-methoxyquinolin-4-yl)propyl]-1-[2-(2-thienylthio)ethyl]piperidine-3-carboxylate were obtained in the form of a colorless oil.

출처