ClC1C=C(C2C=CC([C@H](N)C)=CC=2)C(OC)=NC=1.BrC1C=CC([C@H](NC(=O)O)C)=CC=1.ClC1C=CC(OC)=C(B(O)O)C=1.[Cl:44][C:45]1[CH:46]=[CH:47][C:48]([O:60][CH3:61])=[C:49]([C:51]2[CH:56]=[CH:55][C:54]([C@H:57]([NH2:59])[CH3:58])=[CH:53][CH:52]=2)[CH:50]=1.[F:62][C:63]1[CH:64]=[C:65]([S:70](Cl)(=[O:72])=[O:71])[CH:66]=[CH:67][C:68]=1[F:69]>>[Cl:44][C:45]1[CH:46]=[CH:47][C:48]([O:60][CH3:61])=[C:49]([C:51]2[CH:56]=[CH:55][C:54]([C@H:57]([NH2:59])[CH3:58])=[CH:53][CH:52]=2)[CH:50]=1.[Cl:44][C:45]1[CH:46]=[CH:47][C:48]([O:60][CH3:61])=[C:49]([C:51]2[CH:56]=[CH:55][C:54]([C@H:57]([NH:59][S:70]([C:65]3[CH:66]=[CH:67][C:68]([F:69])=[C:63]([F:62])[CH:64]=3)(=[O:72])=[O:71])[CH3:58])=[CH:53][CH:52]=2)[CH:50]=1(R)-1-(5′-Chloro-2′-methoxy-biphenyl-4-yl)-ethylamine was prepared in a similar manner to (R)-1-[4-(5-chloro-2-methoxypyridin-3-yl)-phenyl]ethylamine (Example 39) starting from (R)-[1-(4-bromophenyl)-ethyl]-carbamic acid and 5-chloro-2-methoxyphenylboronic acid. The title compound was prepared in a similar manner to (R)-1-Methyl-3-trifluoromethyl-1H-pyrazole-4-sulfonic acid 1-{[4-(5-chloro-2-methoxypyridin-3-yl)-phenyl]-ethyl}-amide (Example 39) using (R)-1-(5′-chloro-2′-methoxy-biphenyl-4-yl)-ethylamine and 3,4-difluorobenzenesulfonyl chloride. 1H NMR (400 MHz, CDCl3): 7.52-7.42 (m, 2H), 7.35-7.08 (m, 7H), 6.90 (m, 1H), 4.80 (d, 1H), 4.60 (q, 1H), 3.79 (s, 3H), 1.51 (d, 3H) ppm.
Wird geladen…