Reaktion #74516

Reaktionsgleichung

trifluoroacetic acid

hydrochloric acid

N-(2,4-dimethoxybenzyl)-2,4,5-trifluoro-N-1,2,4-thiadiazol-5-ylbenzenesulfonamide

2-(2-aminopyridin-4-yl)-4-chlorophenol

potassium carbonate

→

title compound

4-[2-(2-aminopyridin-4-yl)-4-chlorophenoxy]-2,5-difluoro-N-1,2,4-thiadiazol-5-ylbenzenesulfonamide

Lösungsmittel

dichloromethane

ethyl acetate

ethyl acetate

dimethyl sulfoxide

Reaktionsbedingungen

Aufarbeitung

1. 1
   SonstigeThe reaction was partitioned between ethyl acetate (150 mL) and saturated aqueous sodium chloride solution (150 mL)
2. 2
   SonstigeThe organic layer was collected
3. 3
   Einengenconcentrated in vacuo
4. 4
   Sonstigeto afford an orange residue
5. 5
   workup.STIRRINGThe reaction was stirred at room temperature for 24 hours
6. 6
   Einengenbefore concentrating in vacuo
7. 7
   Sonstigeto afford a pink residue
8. 8
   Sonstigeto form a white slurry that
9. 9
   Waschenwas washed with saturated sodium bicarbonate solution (200 mL)
10. 10
    FiltrationFiltration
11. 11
    Sonstigeyielded a white solid
12. 12
    Sonstigethat was dried in vacuo
13. 13
    SonstigeThe organic layer was collected
14. 14
    Einengenconcentrated in vacuo

Vorschrift

A suspension of N-(2,4-dimethoxybenzyl)-2,4,5-trifluoro-N-1,2,4-thiadiazol-5-ylbenzenesulfonamide (Preparation 647, 10 g, 22.45 mmol), 2-(2-aminopyridin-4-yl)-4-chlorophenol (Preparation 258, 5 g, 22.67 mmol) and potassium carbonate (3.72 g, 26.94 mmol) in dimethyl sulfoxide (150 mL) was stirred at room temperature for 2 hours. The reaction was partitioned between ethyl acetate (150 mL) and saturated aqueous sodium chloride solution (150 mL). The organic layer was collected and concentrated in vacuo to afford an orange residue. This was dissolved in dichloromethane (145 mL) and trifluoroacetic acid (8.48 mL) was added. The reaction was stirred at room temperature for 24 hours before concentrating in vacuo to afford a pink residue. This was taken up in ethyl acetate (200 mL) to form a white slurry that was washed with saturated sodium bicarbonate solution (200 mL). Filtration yielded a white solid that was dried in vacuo, slurried in water and hydrochloric acid (1 N aqueous solution, 1.05 eq) and extracted with ethyl acetate. The organic layer was collected and concentrated in vacuo to yield the title compound.

Quelle