Methyl 2-[4-(aminomethyl)-3-fluorophenoxy]acetate → (R)-2-[4-({[2-(Benzo[1,3]dioxol-5-yloxy)-5-fluoro-pyridine-3-carbonyl]-amino}-methyl)-3-fluoro-phenoxy]-propionic acid methyl ester
反応式
[O:1]1[C:5]2[CH:6]=[CH:7][C:8]([O:10][C:11]3[N:19]=[CH:18][C:17]([F:20])=[CH:16][C:12]=3[C:13]([OH:15])=O)=[CH:9][C:4]=2[O:3][CH2:2]1.[CH3:21][O:22][C:23](=[O:36])[C@H:24]([O:26][C:27]1[CH:32]=[CH:31][C:30]([CH2:33][NH2:34])=[C:29]([F:35])[CH:28]=1)[CH3:25].COC(=O)COC1C=CC(CN)=C(F)C=1>>[CH3:21][O:22][C:23](=[O:36])[C@H:24]([O:26][C:27]1[CH:32]=[CH:31][C:30]([CH2:33][NH:34][C:13]([C:12]2[C:11]([O:10][C:8]3[CH:7]=[CH:6][C:5]4[O:1][CH2:2][O:3][C:4]=4[CH:9]=3)=[N:19][CH:18]=[C:17]([F:20])[CH:16]=2)=[O:15])=[C:29]([F:35])[CH:28]=1)[CH3:25]参加物
4
反応物 3
生成物 1
実験手順
The compound of Formula (5.0.32) was prepared in a manner analogous to that described in Preparation 20, substituting 2-(benzo[1,3]dioxol-5-yloxy)-5-fluoro-nicotinic acid and (R)-2-(4-aminomethyl-3-fluoro-phenoxy)-propionic acid methyl ester for the corresponding 2-(benzo-[[1,3]-dioxol-5-yloxy)-nicotinic acid and (4-aminomethyl-3-fluoro-phenoxy)-acetic acid methyl ester materials, respectively.
後処理
- customthat described in Preparation 20
出典と根拠
- ORDレコード
- ord-0dce3e1866bb4bc78492428e2b755f2e
- 出典データセット
- uspto-grants-2007_02
- 特許番号
- US07183293B2
反応ノート
読み込み中…