Hydrochloric Acid → HCID 69479868、化合物

HRID 856157ノート

反応式

HRID 856157 の反応式
[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

6

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

  1. temperatureThe mixture was cooled on ice-bath
  2. stirringthe mixture was stirred for 30 minutes
  3. customInsoluble matters were removed by filtration
  4. concentrationthe filtrate was concentrated under reduced pressure
  5. additionEthyl acetate (3.4 ml) and toluene (34 ml) were added to the residue
  6. customthe resulting precipitates
  7. 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

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