1,1-Dimethylethyl 3-[5-(5-{3-cyano-4-[(cyclopropylmethyl)oxy]phenyl}-1,2,4-oxadiazol-3-yl)-1-isoquinolinyl]propanoate → 3-[5-(5-{3-Cyano-4-[(cyclopropylmethyl)oxy]phenyl}-1,2,4-oxadiazol-3-yl)-1-isoquinolinyl]propanoic acid
反応式
[C:1]([C:3]1[CH:4]=[C:5]([C:14]2[O:18][N:17]=[C:16]([C:19]3[CH:28]=[CH:27][CH:26]=[C:25]4[C:20]=3[CH:21]=[CH:22][N:23]=[C:24]4[CH2:29][CH2:30][C:31]([O:33]C(C)(C)C)=[O:32])[N:15]=2)[CH:6]=[CH:7][C:8]=1[O:9][CH2:10][CH:11]1[CH2:13][CH2:12]1)#[N:2]>Cl.O1CCOCC1.CN1CCCC1=O>[C:1]([C:3]1[CH:4]=[C:5]([C:14]2[O:18][N:17]=[C:16]([C:19]3[CH:28]=[CH:27][CH:26]=[C:25]4[C:20]=3[CH:21]=[CH:22][N:23]=[C:24]4[CH2:29][CH2:30][C:31]([OH:33])=[O:32])[N:15]=2)[CH:6]=[CH:7][C:8]=1[O:9][CH2:10][CH:11]1[CH2:13][CH2:12]1)#[N:2]参加物
5
反応物 1
生成物 1
試薬・触媒・溶媒 3
実験手順
1,1-Dimethylethyl 3-[5-(5-{3-cyano-4-[(cyclopropylmethyl)oxy]phenyl}-1,2,4-oxadiazol-3-yl)-1-isoquinolinyl]propanoate (D48; 36 mg, 0.072 mmol) was dissolved in 4N HCl in 1,4-dioxane (4 ml) and the mixture was allowed to stand at room temperature for 4.5 h. The solvent was evaporated in vacuo and the residue triturated with dry ether to give a white solid which was dissolved in N-methyl-2-pyrrolidinone (1 ml) and purified by Mass Directed Preparative HPLC (Supelcosil ABZ+Plus column, eluting with solvents A/B (A: Water+0.1% Formic acid, B: MeCN:Water 95:5+0.05% Formic acid)). The solvent was dried under a stream of nitrogen to give the title compound as a white solid (10.5 mg)
後処理
- customThe solvent was evaporated in vacuo
- customthe residue triturated with dry ether
- customto give a white solid which
- custompurified by Mass Directed Preparative HPLC (Supelcosil ABZ+Plus column
- washeluting with solvents A/B (A: Water+0.1% Formic acid, B
- customThe solvent was dried under a stream of nitrogen
出典と根拠
- ORDレコード
- ord-95350a07e7b243f4bd751b74783c9c5c
- 出典データセット
- uspto-grants-2012_12
- 特許番号
- US08329730B2
反応ノート
読み込み中…