189531. lajstromszámú szabadalom • Eljárás alanin-származékok előállítására

189 531 Szám n R‘ R2 R3 MMR spektrum 247 0-ch3 O H Il 1 —CH2—CH2—C—N— —(4-etoxi-fenil)-c2h5 A 7,3-6,4m (8H); 3,6q (3H); 2,lm (2H); 1,5m (2H) 248 0-ch3 —ch2—ch2— H 1 —CON—CH(CH3)2-c2h5 A 2,8-2,2m (3H); 1,5m (2H): l,2d (3H); l,0d (6H) 249 0-ch3 H 1 —CH2—CH,—CON — —CH2-fenil-c2h5 A 7,4—6,5m (9H); 5.1--4,3m + s (5H); 2,lm (2H); l,5m (211): 1 »2d (3H) 250 0-ch3 —ch2—ch2—coh— 1 N —ch2—ch2— (3,4-dimetoxi-fenil) —C2Hs A 7,3-6,2m (7H); 3,9s (6H): 2.9-2.lm (6H); 1,5m (2H): 1.2d (3H) 251 !-ch3 —CH2—CH,-fenil-c2h5 B 7.2bs (9H): 2.6m (2H): l,7m (2H); l,2d (3H) 252 1 —ch3 — CH2—CH,-fenil — H B 7,2bs (9H): 2,6m (2H); 1.7m (2H) 253 1-ch3 —CHj— CH,— (2-meii|­­fenil)-c\h5 B 7,4-7,0m (8H); 2,6m (2H); 2.3s (3H); 1.7m (2H); 1.2d (3H) 254 1 HO—CH2— — CH2—CH2-fenil —c,h5 B 7,2bs (9H); 2,8-2,5m (4H); 1,7m (2H) 255 1 H,N — -(CH2)4— — CH2—CH2-fenil — H B 7,2bs (9H); 2,8-2,3m (4H): l,8-l,3m (8H) 256 1 H2N(CH2)3 —CH2—CH,— (3-nitro­­fenil) —H B 8,2-7,lm (8H); 2,8-2,3m (4H); 1,8-1,3m (6H) 257 1 —ch3 —ch2—ch2 —(4-klór-fenil) —C,HS B 7,5-6,9m (8H); 2,7m (2H): l,7m (2H); l,2d (3H) 258 1-ch3 —CH2—CH,— (4-klór­­fenil) — H B 7,5-6,9m (8H); 2,7m (2H); l,7m (2H); l,2d (3H) 259 1-ch3 —CH2—CH2 —(4-benzoe­­sav) —H B 7,8-7,lm (8H); 2,7m (2H): l,7m (2H); l,2d (3H) 260 1 HN^r — NH — —(CH2)4— —CH2—CH2—(4-klór­­fenil) —CHS B 7,5-7,0 (8H); 2,8-2.om 44li,; l,7-l,3m (6H) 261 1 h2n— —(CH2)2— —CH2—CH2—(4-hidroxi­­fenil) — H B 7,2-6,5m (8H): 2.8 2.3m (4H); l,7-l,3m (4H) 262 1 h2n—-(CH2)s— —CH2—CH2-fenil — H B 7,2bs (9H); 2,7-2.?m dl!,. l,7-l,2m (10H) 263 1 h2n— —(CH2)4— —CH2—CH,— (4-karba­­moil-fenil) — H B 7,8-7,lm (8H); 2,?~-2.3m (4H); l,8-l,3m (8H) 264 1 H2N—CH2— —CH2—CH2-fenil —H B 7,2bs (9H); 2.7-2.3m (411): 1,7m (2H) 265 1-ch3 —CH2—CH,— (4-fluor­­fenil)-c2h5 B 7,2-6,8m (8111: 2.7m (2111: 1,7m (2H): 1.2d (311)

Next

/
Oldalképek
Tartalom