Reaktion #73567

Reaktionsgleichung

Isopropyl acetate

(2S,3R)—N-(2-((3-Pyridinyl)methyl)-1-azabicyclo[2.2.2]octan-3-yl)benzofuran-2-carboxamide

dichloromethane

p-Toluenesulfonic acid

→

(2S,3R)—N-(2-((3-pyridinyl)methyl)-1-azabicyclo[2.2.2]oct-3-yl)benzofuran-2-carboxamide p-toluenesulfonate

Ausbeute 92.4%

Lösungsmittel

Water

Reaktionsbedingungen

Aufarbeitung

1. 1
   EinengenThe solution was concentrated to an oil, acetone (4 L)
2. 2
   workup.ADDITIONwas added
3. 3
   Einengenthe mixture was concentrated to an oily solid
4. 4
   workup.ADDITIONAdditional acetone (12 L) was added to the oily solid in the rotary evaporator bulb
5. 5
   Sonstigethe resulting slurry was transferred to a 50 L glass reaction flask with a mechanical stirrer, condenser
6. 6
   TemperaturThe reaction mixture was heated to 50° C.±5° C
7. 7
   workup.ADDITIONwas added to the reaction mixture in portions over approximately 15 min
8. 8
   TemperaturThe reaction mixture was heated
9. 9
   Temperaturto reflux
10. 10
    Sonstigeheld at that temperature for a minimum of 30 min
11. 11
    Sonstigeto obtain a solution
12. 12
    TemperaturThe reaction was cooled to 40° C.±5° C. over approximately 2 h
13. 13
    FiltrationThe mixture was filtered
14. 14
    Waschenthe filter cake was washed with isopropyl acetate (3.5 L)
15. 15
    SonstigeThe isolated product was dried under vacuum at 105° C.±5° C. for between 2 h and 9 h

Vorschrift

(2S,3R)—N-(2-((3-Pyridinyl)methyl)-1-azabicyclo[2.2.2]octan-3-yl)benzofuran-2-carboxamide (1.62 kg, 4.48 mol) and dichloromethane (8.60 kg) were added into a carboy. The weight/weight percent of the material in solution was determined through HPLC analysis. The solution was concentrated to an oil, acetone (4 L) was added, and the mixture was concentrated to an oily solid. Additional acetone (12 L) was added to the oily solid in the rotary evaporator bulb, and the resulting slurry was transferred to a 50 L glass reaction flask with a mechanical stirrer, condenser, temperature probe, and condenser under an inert atmosphere. The reaction mixture was heated to 50° C.±5° C. Water (80.7 g) was added to the solution, and it was stirred for a minimum of 10 min. p-Toluenesulfonic acid (853 g, 4.44 mol) was added to the reaction mixture in portions over approximately 15 min. The reaction mixture was heated to reflux and held at that temperature for a minimum of 30 min to obtain a solution. The reaction was cooled to 40° C.±5° C. over approximately 2 h. Isopropyl acetate (14.1 L) was added over approximately 1.5 h. The reaction mixture was slowly cooled to ambient temperature over a minimum of 10 h. The mixture was filtered and the filter cake was washed with isopropyl acetate (3.5 L). The isolated product was dried under vacuum at 105° C.±5° C. for between 2 h and 9 h to give 2.19 kg (88.5% yield) of (2S,3R)—N-(2-((3-pyridinyl)methyl)-1-azabicyclo[2.2.2]oct-3-yl)benzofuran-2-carboxamide p-toluenesulfonate, mp 226-228° C. 1H NMR (500 MHz, D2O) δ 8.29 (s, 1H), 7.78 (m, J=5.1, 1H), 7.63 (d, J=7.9, 1H), 7.54 (d, J=7.8, 1H), 7.49 (d, J=8.1, 2H), 7.37 (m, J=8.3, 1H), 7.33 (m, J=8.3, 6.9, 1.0, 1H), 7.18 (m, J=7.8, 6.9, 1.0, 1H), 7.14 (d, J=8.1, 2H), 7.09 (s, 1H), 6.99 (dd, J=7.9, 5.1, 1H), 4.05 (m, J=7.7, 1H), 3.74 (m, 1H), 3.47 (m, 2H), 3.28 (m, 1H), 3.22 (m, 1H), 3.15 (dd, J=13.2, 4.7, 1H), 3.02 (dd, J=13.2, 11.5, 1H), 2.19 (s, 3H), 2.02 (m, 2H), 1.93 (m, 2H), 1.79 (m, 1H). 13C NMR (126 MHz, D2O) δ 157.2, 154.1, 150.1, 148.2, 146.4, 145.2, 138.0, 137.0, 130.9, 128.2 (2), 126.9, 126.8, 125.5 (2), 123.7, 123.3, 122.7, 111.7, 100.7, 61.3, 50.2, 48.0, 40.9, 33.1, 26.9, 21.5, 20.8, 17.0.

Quelle