Reaction #86681

Reaction equation

6-(3-tert-butyl-5-(2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)-2-methoxyphenyl)naphthalen-2-yl 1,1,2,2,3,3,4,4,4-nonafluorobutane-1-sulfonate

methanesulfonamide

di-tert-butyl(2′,4′,6′-triisopropyl-3,4,5,6-tetramethylbiphenyl-2-yl)phosphine

potassium phosphate tribasic

→

title compound

Yield 73.0%

N-(6-(3-tert-butyl-5-(2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)-2-methoxyphenyl)naphthalen-2-yl)methanesulfonamide

Yield 73.0%

Solvents

t-amyl alcohol

Conditions

Workup

1. 1
   workup.ADDITIONwere charged to the 3-L flask
2. 2
   OtherThe flask was purged with argon for not less than 90 minutes
3. 3
   workup.ADDITIONt-Amyl alcohol (250 ml) was charged to a separate 500-mL round-bottom flask
4. 4
   Otherwas purged with argon for not less than 30 minutes
5. 5
   workup.STIRRINGstirred at this temperature for 30 minutes
6. 6
   OtherA 1-L round-bottom flask equipped with a magnetic stir bar
7. 7
   Otherpurged with argon
8. 8
   Temperatureheated to 60° C
9. 9
   workup.STIRRINGThe reagent mixture was stirred under argon for not less than 30 minutes
10. 10
    TemperatureThe temperature of the 3-L flask was raised to 85° C.
11. 11
    workup.STIRRINGthe contents were stirred for 14 hours under a positive pressure of argon
12. 12
    TemperatureThe temperature was then raised to 95° C.
13. 13
    workup.STIRRINGthe contents were stirred for an additional 4 hours under a positive pressure of argon
14. 14
    Temperatureto cool down to room temperature
15. 15
    workup.ADDITIONdiluted with tetrahydrofuran (2200 mL) and water (800 mL)
16. 16
    Otherwas transferred to a 6-L separatory funnel
17. 17
    WashThe organic layer was washed thrice with water (2000 mL)
18. 18
    workup.ADDITIONcontaining L-cysteine (17.3 g) and NaCl (235 g)
19. 19
    OtherThe organic layer was collected
20. 20
    Filtrationfiltered through a pad of diatomaceous earth
21. 21
    Concentrationwas concentrated in vacuo to approximately 250 mL
22. 22
    workup.ADDITIONEthyl acetate (775 mL) was added over 7 hours
23. 23
    workup.STIRRINGwith stirring
24. 24
    workup.STIRRINGto stir for an additional 14 hours
25. 25
    OtherWhite solid was isolated by filtration
26. 26
    Washthe solid was washed with ethyl acetate (1000 mL)
27. 27
    workup.DISSOLUTIONThe solid was then dissolved in tetrahydrofuran (1500 mL)
28. 28
    Filtrationfiltered through a pad of diatomaceous earth
29. 29
    Otherto obtain a clear solution
30. 30
    WashThe diatomaceous earth was washed with tetrahydrofuran (300 mL)
31. 31
    ConcentrationThe combined tetrahydrofuran solution was concentrated in vacuo to approximately 250 mL
32. 32
    workup.ADDITIONethyl acetate (775 mL) was added over 7 hours
33. 33
    workup.STIRRINGwith stirring
34. 34
    workup.STIRRINGto stir for an additional 14 hours
35. 35
    OtherWhite solid was isolated by filtration
36. 36
    WashThe solid was washed with ethyl acetate (1000 mL)
37. 37
    Otherdried in a vacuum oven at 60° C. for 24 hours
38. 38
    Otherisolated by filtration
39. 39
    WashThe solid was washed with 132 mL of 200 proof ethanol
40. 40
    Otherdried in a vacuum oven at 50° C. for 18 hours

Procedure

A 3-L, 3-neck, round-bottom flask was equipped with an overhead stirrer, a thermocouple, a Claisen condenser and a reflux condenser. Tris(dibenzylideneacetone)dipalladium(0) (0.330 g, 0.360 mmol), di-tert-butyl(2′,4′,6′-triisopropyl-3,4,5,6-tetramethylbiphenyl-2-yl)phosphine (0.416 g, 0.864 mmol) and milled potassium phosphate tribasic (21.0 g, 99.0 mmol) were charged to the 3-L flask. The flask was purged with argon for not less than 90 minutes with constant stirring of the solids. t-Amyl alcohol (250 ml) was charged to a separate 500-mL round-bottom flask and was purged with argon for not less than 30 minutes and was transferred to the 3-L flask using a cannula under argon atmosphere. The contents of the 3-L flask were heated to 80° C. and stirred at this temperature for 30 minutes. A 1-L round-bottom flask equipped with a magnetic stir bar was charged with 6-(3-tert-butyl-5-(2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)-2-methoxyphenyl)naphthalen-2-yl 1,1,2,2,3,3,4,4,4-nonafluorobutane-1-sulfonate (62.9 g, 90 mmol), methanesulfonamide (12.85 g, 135 mmol) and t-amyl alcohol (505 mL), purged with argon and heated to 60° C. The reagent mixture was stirred under argon for not less than 30 minutes. A clear yellow solution was observed. This solution was transferred to the 3-L flask using a cannula under argon atmosphere. The temperature of the 3-L flask was raised to 85° C. and the contents were stirred for 14 hours under a positive pressure of argon. The temperature was then raised to 95° C. and the contents were stirred for an additional 4 hours under a positive pressure of argon. The reaction mixture was allowed to cool down to room temperature, diluted with tetrahydrofuran (2200 mL) and water (800 mL) and was transferred to a 6-L separatory funnel. The organic layer was washed thrice with water (2000 mL) containing L-cysteine (17.3 g) and NaCl (235 g). The organic layer was collected, filtered through a pad of diatomaceous earth and was concentrated in vacuo to approximately 250 mL. Ethyl acetate (775 mL) was added over 7 hours with stirring, and the mixture was allowed to stir for an additional 14 hours. White solid was isolated by filtration, and the solid was washed with ethyl acetate (1000 mL). The solid was then dissolved in tetrahydrofuran (1500 mL) and filtered through a pad of diatomaceous earth to obtain a clear solution. The diatomaceous earth was washed with tetrahydrofuran (300 mL). The combined tetrahydrofuran solution was concentrated in vacuo to approximately 250 mL, and then ethyl acetate (775 mL) was added over 7 hours with stirring. The product solution was allowed to stir for an additional 14 hours. White solid was isolated by filtration. The solid was washed with ethyl acetate (1000 mL) and dried in a vacuum oven at 60° C. for 24 hours. The solid was slurried in 308 mL of 200 proof ethanol for 1.5 hours, then isolated by filtration. The solid was washed with 132 mL of 200 proof ethanol and dried in a vacuum oven at 50° C. for 18 hours. The title compound was isolated as a white solid (32.6 g, 100% potency vs. standard, 73% yield). 1H NMR (400 MHz, DMSO-d6) δ ppm 11.41 (d, J=2.1 Hz, 1H), 10.04 (s, 1H), 8.02 (d, J=0.9 Hz, 1H), 7.98-7.91 (m, 2H), 7.79 (d, J=7.9 Hz, 1H), 7.72 (d, J=2.0 Hz, 1H), 7.69 (dd, J=8.5, 1.7 Hz, 1H), 7.41 (dd, J=8.8, 2.2 Hz, 1H), 7.36 (d, J=2.7 Hz, 1H), 7.31 (d, J=2.7 Hz, 1H), 5.65 (dd, J=7.9, 2.2 Hz, 1H), 3.24 (s, 3H), 3.08 (s, 3H), 1.42 (s, 9H). 13C NMR (101 MHz, DMSO-d6) δ ppm 163.1 (C), 156.0 (C), 150.0 (C), 145.3 (CH), 142.9 (C), 136.0 (C), 134.3 (C), 134.2 CO, 133.5 (C), 132.2 (C), 129.5 (C), 129.0 (CH), 127.6 (CH), 127.1 (CH), 127.0 (CH), 126.5 (CH), 124.3 (CH), 120.2 (CH), 114.5 (CH), 101.1 (CH), 60.3 (CH3), 39.4 (CH3), 35.1 (C), 30.5 (CH3).

Source