C1(C)C=CC(S([N:10]2[CH2:15][C@@H:14]3[CH2:16][C@H:11]2[CH2:12][N:13]3[CH2:17][C:18]2[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=2)(=O)=O)=CC=1.Br>C(O)(=O)C>[CH2:17]([N:13]1[CH2:12][C@@H:11]2[CH2:16][C@H:14]1[CH2:15][NH:10]2)[C:18]1[CH:19]=[CH:20][CH:21]=[CH:22][CH:23]=1A mixture of (1S,4S)-2-(4-toluenesulfonyl)-5-phenylmethyl-2,5-diazabicyclo[2.2.1]heptane (54.9 g) in acetic acid (830 mL) containing hydrobromic acid (30% wt) was heated at 70° C. for 18 h. The reaction mixture was allowed to cool and concentrated under reduced pressure to a final volumen of ca. 300 mL. The precipitate that formed was filtered and washed with acetone to give (1S,4S)-N-benzyl-2,5-diazabicyclo[2.2.1]heptane (50.30 g 91.3%, m.p. 272-275° C.).
Wird geladen…