Acetonitrile → HCID 638695、化合物

HRID 1350690ノート

反応式

HRID 1350690 の反応式
I.[CH3:2][NH:3][C:4](=[NH:7])[S:5][CH3:6].Br[C:9](=[CH:12][O:13]C(C)C)[CH:10]=[O:11].CC#N.C([O-])([O-])=O.[K+].[K+]>O>[CH3:2][N:3]1[C:9]([CH:10]=[O:11])=[CH:12][N:7]=[C:4]1[S:5][CH3:6].[CH3:2][N:3]1[CH:10]=[C:9]([CH:12]=[O:13])[N:7]=[C:4]1[S:5][CH3:6]

参加物

7

反応物 4

HCID 6342AcetonitrileHCID 11430Potassium CarbonateHCID 534166342-Bromo-3-isopropoxy-propenalHCID 178485204HCID 178485204、化合物

生成物 2

HCID 638695HCID 638695、化合物HCID 210972441H-Imidazole-4-carboxaldehyde, 1-methyl-2-(methylthio)- (9CI)

試薬・触媒・溶媒 1

HCID 962Water溶媒

反応条件

温度
35 °C

実験手順

To a mixture of 2.65 g (11.4 mmol) of 1,2-dimethyl-isothiourea hydroiodide and 1.00 g (10.4 mmol) of 2-bromo-3-isopropoxy-propenal 8 mL of MeCN was added 1.58 g (11.4 mmol) of K2CO3 (Shilcrat, S. C. et al. J. Org. Chem., 1997, 62, 8449–8454). The mixture was stirred at 35° C. under N2 for 16 h, water (20 ml) was added, and the mixture was extracted with CH2Cl2 (200 mL). The extract was dried over MgSO4, filtered, concentrated, and chromatographed (0 to 100% EtOAc in hexanes) to provide 1.09 g of 3-methyl-2-methylsulfanyl-3H-imidazole-4-carbaldehyde and 284 mg of 1-methyl-2-methylsulfanyl-1H-imidazole-4-carbaldehyde.

後処理

  1. extractionthe mixture was extracted with CH2Cl2 (200 mL)
  2. dry with materialThe extract was dried over MgSO4
  3. filtrationfiltered
  4. concentrationconcentrated
  5. customchromatographed (0 to 100% EtOAc in hexanes)

出典と根拠

ORDレコード
ord-aa359d021bd04eb1a0f5790763575632
出典データセット
uspto-grants-2007_05
特許番号
US07214802B2

反応ノート

読み込み中…