2-(Methoxymethyl)-2'-methylbiphenyl-4-carboxylic acid → (3-{5-[2-(Methoxymethyl)-2'-methylbiphenyl-4-yl]-1,2,4-oxadiazol-3-yl}phenyl)methanol
反応式
[CH3:1][O:2][CH2:3][C:4]1[CH:9]=[C:8]([C:10]([OH:12])=O)[CH:7]=[CH:6][C:5]=1[C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][C:14]=1[CH3:19].O[N:21]=[C:22]([NH2:31])[C:23]1[CH:28]=[CH:27][CH:26]=[C:25]([CH2:29][OH:30])[CH:24]=1>>[CH3:1][O:2][CH2:3][C:4]1[CH:9]=[C:8]([C:10]2[O:12][N:31]=[C:22]([C:23]3[CH:24]=[C:25]([CH2:29][OH:30])[CH:26]=[CH:27][CH:28]=3)[N:21]=2)[CH:7]=[CH:6][C:5]=1[C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][C:14]=1[CH3:19]参加物
3
実験手順
The title compound was prepared following the general procedure 3 starting from Intermediate 3 and Intermediate 70 and was isolated as a yellow oil. HPLC (Method A) Rt 5.16 min (Purity: 97.0%).
後処理
- customwas isolated as a yellow oil
出典と根拠
- ORDレコード
- ord-2a733703ea6b4180b55427e33933af88
- 出典データセット
- uspto-grants-2014_08
- 特許番号
- US08815919B2
反応ノート
読み込み中…