Hydrochloric Acid → HCID 69479868、化合物
反応式
[Cl:1][C:2]1[N:3]([CH2:10][C@@:11]([OH:26])([CH3:25])[CH2:12][O:13]C(=O)C2C=CC([N+]([O-])=O)=CC=2)[CH:4]=[C:5]([N+:7]([O-:9])=[O:8])[N:6]=1.Cl.S([O-])([O-])(=O)=O.[Mg+2]>CO.C(=O)([O-])[O-].[K+].[K+]>[Cl:1][C:2]1[N:3]([CH2:10][C@@:11]([OH:26])([CH3:25])[CH2:12][OH:13])[CH:4]=[C:5]([N+:7]([O-:9])=[O:8])[N:6]=1参加物
実験手順
(S)-2-Chloro-4-nitro-1-[2-hydroxy-3-(4-nitrobenzoyloxy)-2-methylpropyl]imidazole prepared in Example 15 (6.8 g, 17.67 mmol) was dissolved in methanol (68 ml). Potassium carbonate (122 mg, 0.88 mmol) was added to the solution, and the resulting mixture was stirred at room temperature overnight. The mixture was cooled on ice-bath, 6N hydrochloric acid (0.3 ml) and magnesium sulfate (3 g) were added to the mixture in this order, and the mixture was stirred for 30 minutes. Insoluble matters were removed by filtration, and the filtrate was concentrated under reduced pressure. Ethyl acetate (3.4 ml) and toluene (34 ml) were added to the residue, and the resulting precipitates were filtered off to afford (S)-2-chloro-1-(2,3-dihydroxy-2-methylpropyl)-4-nitroimidazole (4.09 g, yield 97%) as a yellow powder.
後処理
- temperatureThe mixture was cooled on ice-bath
- stirringthe mixture was stirred for 30 minutes
- customInsoluble matters were removed by filtration
- concentrationthe filtrate was concentrated under reduced pressure
- additionEthyl acetate (3.4 ml) and toluene (34 ml) were added to the residue
- customthe resulting precipitates
- filtrationwere filtered off
出典と根拠
- ORDレコード
- ord-770b5bd5350e41968cbd00c66484b1fc
- 出典データセット
- uspto-grants-2007_08
- 特許番号
- US07262212B2
反応ノート
読み込み中…