Reaktion #9693

Reaktionsgleichung

6-methoxy-2-(methylsulfonyl)-1,3-benzothiazole

6-methoxy-2-(methylsulfonyl)-1,3-benzothiazole

HCl

Methyl (1R,2R)-2-[(4′-amino-3′-fluoro-1,1′-biphenyl-4-yl)carbonyl]cyclo-pentanecarboxylate

n-butanol

→

butyl (1R,2R)-2-({3′-fluoro-4′-[(6-methoxy-1,3-benzothiazol-2-yl)amino]-1,1′-biphenyl-4-yl}carbonyl)cyclopentanecarboxylate

Ausbeute 65.0%

Reaktionsbedingungen

Aufarbeitung

1. 1
   SonstigeSolvent was then removed by rotary evaporation
2. 2
   Sonstigethe residue was purified by flash chromatography (Biotage Flash 40 M, 3:1 hexane/EtOAc)

Vorschrift

Methyl (1R,2R)-2-[(4′-amino-3′-fluoro-1,1′-biphenyl-4-yl)carbonyl]cyclo-pentanecarboxylate (462 mg, 1.35 mmol) was dissolved in n-butanol (15 mL), and 6-methoxy-2-(methylsulfonyl)-1,3-benzothiazole (162 mg, 0.8 mmol) and 4 M aqueous HCl (1.5 mL) were added. The mixture was heated at 90° C. for 5 h. An additional portion of 6-methoxy-2-(methylsulfonyl)-1,3-benzothiazole (162 mg, 0.8 mmol) was added, and the mixture was stirred overnight at 90° C. Solvent was then removed by rotary evaporation, and the residue was purified by flash chromatography (Biotage Flash 40 M, 3:1 hexane/EtOAc) to afford butyl (1R,2R)-2-({3′-fluoro-4′-[(6-methoxy-1,3-benzothiazol-2-yl)amino]-1,1′-biphenyl-4-yl}carbonyl)cyclopentanecarboxylate (480 mg, 65%). LC-MS ret. time 4.36 min, m/z 547.3 (MH+); 1H NMR (300 MHz, CDCl3) δ 0.85 (t, 3H), 1.25–1.35 (m, 2H), 1.40–1.58 (m, 2H), 1.74–1.84 (m, 3H), 1.91–1.96 (m, 1H), 2.11-2.20 (m, 2H), 3.40–3.46 (m, 1H), 3.84 (s, 3H), 4.03 (t, 2H), 6.81–6.87 (m, 1H), 6.98 (dd, 1H), 7.18 (d, 1H), 7.40–7.52 (m, 2H), 7.64 (d, 2H), 8.14 (d, 2H), 8.42 (t, 1H).

Quelle