Phenol → [2,6-Dimethyl-4-(5-phenoxy-oxazolo[5,4-d]pyrimidin-2-yl)-phenoxy]-acetic acid tert-butyl ester
反応式
[H-].[Na+].[C:3]1([OH:9])[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1.[C:10]([O:14][C:15](=[O:36])[CH2:16][O:17][C:18]1[C:23]([CH3:24])=[CH:22][C:21]([C:25]2[O:26][C:27]3[N:28]=[C:29](Cl)[N:30]=[CH:31][C:32]=3[N:33]=2)=[CH:20][C:19]=1[CH3:35])([CH3:13])([CH3:12])[CH3:11]>CC(N(C)C)=O>[C:10]([O:14][C:15](=[O:36])[CH2:16][O:17][C:18]1[C:23]([CH3:24])=[CH:22][C:21]([C:25]2[O:26][C:27]3[N:28]=[C:29]([O:9][C:3]4[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=4)[N:30]=[CH:31][C:32]=3[N:33]=2)=[CH:20][C:19]=1[CH3:35])([CH3:13])([CH3:12])[CH3:11]参加物
反応物 3
生成物 1
試薬・触媒・溶媒 1
実験手順
19 mg of sodium hydride were added under an argon atmosphere to a solution of 38 mg of phenol in 5 ml of dimethylacetamide. After stirring for 30 min at room temperature, a solution of 156 mg of [4-(5-chloro-oxazolo[5,4-d]pyrimidin-2-yl)-2,6-dimethyl-phenoxy]-acetic acid tert-butyl ester in 3 ml of dimethylacetamide was added slowly. The mixture was allowed to stir for 1.5 h at room temperature. Upon consumption of the starting ester an aqueous solution of citric acid (100 g/l) was added until the pH was neutral. The aqueous layer was extracted twice with 15 ml ethyl acetate. The combined organic layers were dried over sodium sulfate, filtered and the solvents were removed in vacuo. The title compound was isolated by silica gel chromatography (heptane/ethyl acetate gradient). Yield: 77 mg of a white solid.
後処理
- stirringto stir for 1.5 h at room temperature
- customUpon consumption of the starting ester an aqueous solution of citric acid (100 g/l)
- additionwas added until the pH
- extractionThe aqueous layer was extracted twice with 15 ml ethyl acetate
- dry with materialThe combined organic layers were dried over sodium sulfate
- filtrationfiltered
- customthe solvents were removed in vacuo
出典と根拠
- ORDレコード
- ord-5894b2320fdc46bc8dee19f753a981e8
- 出典データセット
- uspto-grants-2014_09
- 特許番号
- US08846692B2
反応ノート
読み込み中…