Hydrogen Bromide → 3-[(2-Aminoethyl)thiomethyl]isoxazole hydrobromide
反応式
Cl[CH2:2][C:3]1[CH:7]=[CH:6][O:5][N:4]=1.Cl.[NH2:9][CH2:10][CH2:11][SH:12].[BrH:13]>>[BrH:13].[NH2:9][CH2:10][CH2:11][S:12][CH2:2][C:3]1[CH:7]=[CH:6][O:5][N:4]=1参加物
4
実験手順
A solution of 3-chloromethylisoxazole (5.8 g.) and cysteamine hydrochloride (6.25 g.) in aqueous hydrobromic acid (48%, 100 ml) was heated under reflux for 6 hours. Concentration in the presence of water and subsequently n-propanol, followed by recrystallisation of the residue from isopropyl alcohol-ethanol afforded 3-[(2-aminoethyl)thiomethyl]isoxazole hydrobromide m.p. 131°-133°. (Found: Br, 33.6; S, 13.7. C6H10N2O S. H Br requires: Br, 33.4; S, 13.4).
後処理
- temperatureunder reflux for 6 hours
- concentrationConcentration in the presence of water and subsequently n-propanol
- customfollowed by recrystallisation of the residue from isopropyl alcohol-ethanol
出典と根拠
- ORDレコード
- ord-c27515ac845a49fa8cf8f862d99c459f
- 出典データセット
- uspto-grants-1980_09
- 特許番号
- US04221802
反応ノート
読み込み中…