1-(2-Bromoethyl)-2-methyl-5-nitroimidazole → Tinidazole
反応式
Br[CH2:2][CH2:3][N:4]1[C:8]([N+:9]([O-:11])=[O:10])=[CH:7][N:6]=[C:5]1[CH3:12].[Na].[CH2:14]([S:16]([OH:18])=[O:17])[CH3:15]>CS(C)=O>[CH2:14]([S:16]([CH2:2][CH2:3][N:4]1[C:8]([N+:9]([O-:11])=[O:10])=[CH:7][N:6]=[C:5]1[CH3:12])(=[O:18])=[O:17])[CH3:15]参加物
5
実験手順
5.83 g. (25 m moles) of 1-(2'-bromoethyl)-2-methyl-5-nitroimidazole is dissolved in 50 ml. of dimethylsulfoxide and 5.48 g. (30 m mole) of the sodium salt of ethyl sulfinic acid (CH3CH2SO2Na) is added. The reaction mixture is maintained for 21/2 hours at 100°-110° C. thereafter the solvent is removed under vacuum and the solid residue is washed with water and recrystallized from ethanol. The yield is 2.28 (37%) of 1-[2'-(ethylsulfonyl)-ethyl]-2-methyl-5-nitroimidazole, M.P. 124°-126° C.
後処理
- temperatureThe reaction mixture is maintained for 21/2 hours at 100°-110° C.
- customthe solvent is removed under vacuum
- washthe solid residue is washed with water
- customrecrystallized from ethanol
出典と根拠
- ORDレコード
- ord-7acfe97b781245468d9dddf48f2cda21
- 出典データセット
- uspto-grants-1979_07
- 特許番号
- US04160096
反応ノート
読み込み中…