Hydrogen Bromide → 3-[(2-Aminoethyl)thiomethyl]isoxazole hydrobromide
Reaction equation
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]=1Participants
4
Procedure
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).
Workup
- 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
Sources & evidence
- ORD record
- ord-c6c759d19ba744959a3207668c347249
- Source dataset
- uspto-grants-1977_05
- Patent number
- US04024271
Reaction notes
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