Tetrahydrofuran → 5-Ethyl-2-[2-fluoro-4-(2-hydroxyethylamino)-phenoxy]phenol
反応式
C([O:8][C:9]1[CH:26]=[C:25]([CH2:27][CH3:28])[CH:24]=[CH:23][C:10]=1[O:11][C:12]1[CH:17]=[CH:16][C:15]([NH:18][CH2:19][CH2:20][OH:21])=[CH:14][C:13]=1[F:22])C1C=CC=CC=1.O1CCCC1>CO>[CH2:27]([C:25]1[CH:24]=[CH:23][C:10]([O:11][C:12]2[CH:17]=[CH:16][C:15]([NH:18][CH2:19][CH2:20][OH:21])=[CH:14][C:13]=2[F:22])=[C:9]([OH:8])[CH:26]=1)[CH3:28]参加物
4
実験手順
According to the procedure of example 20(b) except substituting 4-ethyl-2-methoxy-1-[4-nitro-2-(trifluoromethyl)phenoxy]benzene for N-[4-(2-Benzyloxy-4-ethylphenoxy)-3-fluorophenyl]-2-aminoethanol (350 mg, 0.92 mmol) and tetrahydrofurane for methanol (25 mL), the title compound (210 mg; 78%) was obtained as a yellow solid, after purification on silica gel (ethylacetate and petroleum ether: 5/5)
出典と根拠
- ORDレコード
- ord-9e6c68587c0f449ebff65061273f2c2e
- 出典データセット
- uspto-grants-2014_05
- 特許番号
- US08722746B2
反応ノート
読み込み中…