Réaction #8618

Équation de réaction

acetic acid

lithium t-butoxide

[4-(3,6-dihydro-2H-thiopyran-4-yl)-3-fluorophenyl]carbamic acid 2-methylpropyl ester

(S)—N-[2-(acetyloxy)-3-chloropropyl]acetamide

→

title compound

Rendement 78.5%

(S)—N-[[3-[4-(3,6-dihydro-2H-thiopyran-4-yl)-3-fluorophenyl]-2-oxo-5-oxazolidinyl]methyl]acetamide

Rendement 78.5%

Solvants

—

isooctanes

methanol

methanol

N,N-dimethylformamide

toluene

Conditions de réaction

Traitement

1. 1
   TempératureThe mixture is cooled to 0° C.
2. 2
   TempératureThe mixture is warmed to 21° C.
3. 3
   AutreThe phases are separated
4. 4
   Lavagethe upper washed twice with a mixture of methanol (29 ml) and water (9 ml)
5. 5
   workup.ADDITIONis added water (69 ml) and methylene chloride (69 ml)
6. 6
   AutreThe phases are separated
7. 7
   Lavagethe upper phase washed twice with methylene chloride (29 ml)
8. 8
   Concentrationare concentrated under reduced pressure to 112 ml total volume
9. 9
   workup.ADDITIONMethanol (69 ml) is added
10. 10
    Concentrationthe mixture concentrated to 112 ml
11. 11
    workup.ADDITIONMethanol (69 ml) is added
12. 12
    Concentrationthe mixture concentrated to 75 ml
13. 13
    workup.ADDITIONtoluene (65 ml) is added
14. 14
    workup.ADDITIONWater (65 ml) is added over ½ h
15. 15
    Températurewhile maintaining 19 to 30° C
16. 16
    TempératureThe mixture is cooled to 9° C.
17. 17
    workup.ADDITIONisooctanes (56 ml) added
18. 18
    TempératureThe slurry is cooled to 0° C.
19. 19
    Filtrationthe precipitate collected by vacuum filtration
20. 20
    Lavagewashed with water (22 ml) and isooctanes (22 ml)
21. 21
    Autredried in a nitrogen stream

Mode opératoire

To a mixture of [4-(3,6-dihydro-2H-thiopyran-4-yl)-3-fluorophenyl]carbamic acid 2-methylpropyl ester (17.89 g, 57.83 mmol), (S)—N-[2-(acetyloxy)-3-chloropropyl]acetamide (22.35 g, 115.42 mmol, 2.00 eq), methanol (3.66 g, 114 mmol, 1.97 eq), 2,6-di-tert-butyl-4-methylphenol (0.1365 g, 0.6194 mmol, 0.0107 eq), toluene (52 ml), isooctanes (49 ml), and N,N-dimethylformamide (34.3 ml) is added a solution of lithium t-butoxide (13.94 g, 174.1 mmol, 3.01 eq) in isooctanes (130 ml) over 1.6 h while maintaining 15° C. Isooctanes (20 ml) is added and the mixture stirred at 15 to 19° C. for 17 h. The mixture is cooled to 0° C. and acetic acid (6.7 ml, 117 mmol, 2.02 eq) added. The mixture is warmed to 21° C. and methanol (29 ml) added. The phases are separated and the upper washed twice with a mixture of methanol (29 ml) and water (9 ml). To the combined lower phases is added water (69 ml) and methylene chloride (69 ml). The phases are separated and the upper phase washed twice with methylene chloride (29 ml). The combined lower phases are concentrated under reduced pressure to 112 ml total volume. Methanol (69 ml) is added and the mixture concentrated to 112 ml. Methanol (69 ml) is added and the mixture concentrated to 75 ml then toluene (65 ml) is added. Water (65 ml) is added over ½ h while maintaining 19 to 30° C. The mixture is cooled to 9° C. and isooctanes (56 ml) added. The slurry is cooled to 0° C. and the precipitate collected by vacuum filtration, washed with water (22 ml) and isooctanes (22 ml) and dried in a nitrogen stream to give the title compound (15.909 g, 78.5%): HPLC retention time=2.77 min (column=Phenomenex Luna 5.0 micron C-8(12) 150×4.6 mm, flow rate=2.0 ml/min, gradient elution from 40:60 A:B to 73.3:26.7 A:B over 15 minutes; A=acetonitrile; B=water).

Source