反応式
[NH:1]1[C:5]2[CH:6]=[CH:7][C:8]([CH:10]=[N:11]O)=[CH:9][C:4]=2[N:3]=[CH:2]1.[ClH:13]>CO>[ClH:13].[NH:1]1[C:5]2[CH:6]=[CH:7][C:8]([CH2:10][NH2:11])=[CH:9][C:4]=2[N:3]=[CH:2]1参加物
4
実験手順
1H-benzo[d]imidazole-5-formaldehyde oxime (0.55 mmol, 1 eq.) was dissolved in 10 mL methanol and 300 μL of concentrated hydrochloric acid was added. The mixture was flushed with argone and palladium on activated carbon (10% Pd) was added to the solution. The mixture was hydrogenated at 4 bar for 3 hours. The resulted mixture was filtrated through a pad of celite, the solvent was removed and the residue was dried over phosphorus pentoxide in a exsiccator to give a white solid.
後処理
- customThe mixture was flushed with argone and palladium on activated carbon (10% Pd)
- additionwas added to the solution
- filtrationThe resulted mixture was filtrated through a pad of celite
- customthe solvent was removed
- dry with materialthe residue was dried over phosphorus pentoxide in a exsiccator
- customto give a white solid
出典と根拠
- ORDレコード
- ord-710b6adb3c6c4b0f8177d023b04d2a77
- 出典データセット
- uspto-grants-2015_05
- 特許番号
- US09034907B2
関連ノート
読み込み中…