Cyanogen Bromide → 1-[(4-Chlorophenyl)methyl]-4,5-dihydro-1H-imidazol-2-amine hydrochloride
反応式
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([CH2:8][NH:9][CH2:10][CH2:11][NH2:12])=[CH:4][CH:3]=1.[N:13]#[C:14]Br>CO>[ClH:1].[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([CH2:8][N:9]2[CH2:10][CH2:11][N:12]=[C:14]2[NH2:13])=[CH:6][CH:7]=1参加物
4
実験手順
The amine produced in Procedure 90, 14.5 g. (0.079 mole) was dissolved in 50 ml. of methanol and treated with a solution 9.1 g. (0.086 mole) of cyanogen bromide in 30 ml. of methanol in dropwise fashion. The warm solution was cooled to room temperature which resulted in the formation of a precipitate. The mixture was kept with stirring for 1/2 hr. and then a portion of the solvent was removed by distillation in vacuo. The solid product which separated was collected on a filter, washed with Et2O, and air dried, yield 16 g., m.p. 270°-272°.
後処理
- dissolution(0.079 mole) was dissolved in 50 ml
- customresulted in the formation of a precipitate
- customand then a portion of the solvent was removed by distillation in vacuo
- customThe solid product which separated
- customwas collected on a filter
- washwashed with Et2O, and air
- customdried
出典と根拠
- ORDレコード
- ord-88588e1ea8604fde9481a7ede944d609
- 出典データセット
- uspto-grants-1987_02
- 特許番号
- US04642345
反応ノート
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