Potassium Iodide → HCID 86681505、化合物
反応式
C(=O)([O-])[O-].[Cs+].[Cs+].[I-].[K+].[OH:9][N:10]=[C:11]([C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1)[C:12]([NH:14][CH3:15])=[O:13].Cl[CH2:23][C:24]1[N:29]=[C:28]([NH:30][C:31](=[O:37])[O:32][C:33]([CH3:36])([CH3:35])[CH3:34])[CH:27]=[CH:26][CH:25]=1>C(#N)C.CN(C=O)C>[CH3:15][NH:14][C:12](=[O:13])[C:11](=[N:10][O:9][CH2:23][C:24]1[N:29]=[C:28]([NH:30][C:31](=[O:37])[O:32][C:33]([CH3:35])([CH3:34])[CH3:36])[CH:27]=[CH:26][CH:25]=1)[C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1参加物
実験手順
37.4 g (114 mmol) of caesium carbonate and 0.91 g, (5.47 mmol) of potassium iodide were added to a solution of 10.7 g (60.1 mmol) of 2-(hydroxyimino)-N-methyl-2-phenylacetamide (81:19 mixture of the Z and E diastereoisomers) and 13.3 g (54.7 mmol) of tert-butyl [6-(chloromethyl)pyridin-2-yl]carbamate in 100 ml of acetonitrile: DMF 75:25. After stirring for 3 h at room temperature, the mixture was concentrated by evaporation in vacuo and the residue was admixed with 250 ml of ethyl acetate. Then, 500 ml of water were added, the phases were separated and the aqueous phase was extracted again with 250 ml of ethyl acetate. The combined organic phases were dried with MgSO4 and concentrated by evaporation in vacuo. This gave 16.8 g (95% purity; 89:11 mixture of Z and E isomers) of tert-butyl {6-[({[2-(methylamino)-2-oxo-1-phenylethylidene]amino}oxy)methyl]pyridin-2-yl}carbamate.
後処理
- concentrationthe mixture was concentrated by evaporation in vacuo
- additionThen, 500 ml of water were added
- customthe phases were separated
- extractionthe aqueous phase was extracted again with 250 ml of ethyl acetate
- dry with materialThe combined organic phases were dried with MgSO4
- concentrationconcentrated by evaporation in vacuo
出典と根拠
- ORDレコード
- ord-83098e5c023d4086b122e33367fdd4a8
- 出典データセット
- uspto-grants-2014_03
- 特許番号
- US08680283B2
反応ノート
読み込み中…