Hydrochloric Acid → 2-[(3-{4-[(benzyl{2-methyl-3-[(methylsulfonyl)amino]phenyl}amino)methyl]phenoxy}phenoxy)methyl]cyclopropanecarboxylic Acid
反応式
[CH2:1]([N:8]([CH2:21][C:22]1[CH:44]=[CH:43][C:25]([O:26][C:27]2[CH:28]=[C:29]([CH:40]=[CH:41][CH:42]=2)[O:30][CH2:31][CH:32]2[CH2:34][CH:33]2[C:35]([O:37]CC)=[O:36])=[CH:24][CH:23]=1)[C:9]1[CH:14]=[CH:13][CH:12]=[C:11]([NH:15][S:16]([CH3:19])(=[O:18])=[O:17])[C:10]=1[CH3:20])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.Cl.O1CCCC1>O>[CH2:1]([N:8]([CH2:21][C:22]1[CH:23]=[CH:24][C:25]([O:26][C:27]2[CH:28]=[C:29]([CH:40]=[CH:41][CH:42]=2)[O:30][CH2:31][CH:32]2[CH2:34][CH:33]2[C:35]([OH:37])=[O:36])=[CH:43][CH:44]=1)[C:9]1[CH:14]=[CH:13][CH:12]=[C:11]([NH:15][S:16]([CH3:19])(=[O:18])=[O:17])[C:10]=1[CH3:20])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1参加物
5
反応物 3
生成物 1
試薬・触媒・溶媒 1
実験手順
To the product from Example 284A was added 2N hydrochloric acid (1 mL), tetrahydrofuran (0.5 mL) and water (0.5 mL). The reaction mixture was stirred at room temperature overnight. Water (2 mL) was added. The solution was neutralized with 1N hydrochloric aid until pH=2˜3. The product was extracted with ethyl acetate (2 mL), dried in vaccuo, and purified by HPLC to provide the titled compound. 1H NMR (500 MHz, DMSO-d6) δ12.01-12.29 (br.s, 1 H), 8.95 (s, 1 H), 7.23 (m, 8 H), 7.03 (m, 1 H), 6.94 (m, 4 H), 6.69 (m, 1 H), 6.50 (m, 2 H), 4.06 (s, 2 H), 4.03 (s, 2 H), 3.94 (m, 1 H), 3.80 (m, 1 H), 2.91 (s, 3 H), 2.40 (s, 3 H), 1.67 (m, 1 H), 1.57 (m, 1 H), 1.05 (m, 1 H), 0.92 (m, 1 H); MS (APCI+) m/z 587.1 (M+H)+.
後処理
- extractionThe product was extracted with ethyl acetate (2 mL)
- customdried in vaccuo
- custompurified by HPLC
出典と根拠
- ORDレコード
- ord-0160176a53eb4974abc93d73f80a24c4
- 出典データセット
- uspto-grants-2003_06
- 特許番号
- US06583180B2
反応ノート
読み込み中…