3-Amino-3-(3,4-dimethoxyphenyl)propanoic acid → Methyl 3-amino-3-(3-cyclopentyloxy-4-methoxy-phenyl)propionate
反応式
N[CH:2](C1C=CC(OC)=C(OC)C=1)CC(O)=O.[NH2:17][CH:18]([C:23]1[CH:28]=[CH:27][C:26]([O:29][CH3:30])=[C:25]([O:31][CH:32]2[CH2:36][CH2:35][CH2:34][CH2:33]2)[CH:24]=1)[CH2:19][C:20]([OH:22])=[O:21]>>[NH2:17][CH:18]([C:23]1[CH:28]=[CH:27][C:26]([O:29][CH3:30])=[C:25]([O:31][CH:32]2[CH2:33][CH2:34][CH2:35][CH2:36]2)[CH:24]=1)[CH2:19][C:20]([O:22][CH3:2])=[O:21]参加物
3
実験手順
The title compound was prepared following the method for preparing Intermediate 6 except that 3-amino-3-(3,4-dimethoxy-phenyl)propionic acid was substituted with 3-amino-3-(3-cyclopentyloxy-4-methoxy-phenyl)propionic acid. 1H NMR (CDCl3): δ 6.78-6.88 (m, 3H), 4.76 (s, 1H), 4.34 (t, 1H, J=5 Hz), 3.80 (s, 3H), 3.66 (s, 3H), 2.62 (d, 2H, J=5 Hz), 1.82-1.92 (m, 8H), 1.58 (s, 2H).
出典と根拠
- ORDレコード
- ord-f04353b51bce4abf8c90aab1d74f571f
- 出典データセット
- uspto-grants-2013_06
- 特許番号
- US08466191B2
反応ノート
読み込み中…