Hydrochloric Acid → (R)-3-(2-((2-(8-(benzyloxy)-2-oxo-1,2-dihydroquinolin-5-yl)-2-((tert-butyldimethylsilyl)oxy)ethyl)amino)-2-methylpropyl)benzoic acid
反応式
[Li+].[OH-].[CH2:3]([O:10][C:11]1[CH:12]=[CH:13][C:14]([C@@H:22]([O:39][Si:40]([C:43]([CH3:46])([CH3:45])[CH3:44])([CH3:42])[CH3:41])[CH2:23][NH:24][C:25]([CH3:38])([CH3:37])[CH2:26][C:27]2[CH:28]=[C:29]([CH:34]=[CH:35][CH:36]=2)[C:30]([O:32]C)=[O:31])=[C:15]2[C:20]=1[NH:19][C:18](=[O:21])[CH:17]=[CH:16]2)[C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1.Cl>C1COCC1.CO.O>[CH2:3]([O:10][C:11]1[CH:12]=[CH:13][C:14]([C@@H:22]([O:39][Si:40]([C:43]([CH3:46])([CH3:45])[CH3:44])([CH3:42])[CH3:41])[CH2:23][NH:24][C:25]([CH3:38])([CH3:37])[CH2:26][C:27]2[CH:28]=[C:29]([CH:34]=[CH:35][CH:36]=2)[C:30]([OH:32])=[O:31])=[C:15]2[C:20]=1[NH:19][C:18](=[O:21])[CH:17]=[CH:16]2)[C:4]1[CH:5]=[CH:6][CH:7]=[CH:8][CH:9]=1参加物
5
反応物 3
生成物 1
試薬・触媒・溶媒 1
実験手順
Solid LiOH (370 mg, 15.4 mmol) was added to a stirring solution of Intermediate 100 (950 mg, 1.55 mmol) in THF/MeOH/H2O (15 mL, 3/1/1) at rt. The reaction mixture was stirred over night then pH was adjusted to 1 with 1 N HCl. The aqueous layer was extracted with EtOAc and the combined organic layers were washed with brine, dried over Na2SO4, and concentrated to give crude acid (1.09 g) as yellow solid. Recrystallization (CH2Cl2/Et2O) afforded the title compound (830 mg, 89%) as off white solid. ES/MS calcd. for C35H45N2O5Si+ 601.3. Found m/z=601.3 (M+H)+.
後処理
- extractionThe aqueous layer was extracted with EtOAc
- washthe combined organic layers were washed with brine
- dry with materialdried over Na2SO4
- concentrationconcentrated
- customto give crude acid (1.09 g) as yellow solid
- customRecrystallization (CH2Cl2/Et2O)
出典と根拠
- ORDレコード
- ord-c2e21407c62f40b5abd727416d2566ad
- 出典データセット
- uspto-grants-2013_03
- 特許番号
- US08394829B2
反応ノート
読み込み中…