Hydrogen Bromide → HCID 22726020, compound
Reaction equation
[NH2:1][C:2]1[S:3][C:4]2[CH2:10][CH:9]([NH:11][CH2:12][CH2:13][CH3:14])[CH2:8][CH2:7][C:5]=2[N:6]=1.[BrH:15]>CO>[BrH:15].[NH2:1][C:2]1[S:3][C:4]2[CH2:10][CH:9]([NH:11][CH2:12][CH2:13][CH3:14])[CH2:8][CH2:7][C:5]=2[N:6]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
4.00 g of (±)-2-amino-6-propylamino-4,5,6,7-tetrahydrobenzothiazole was dissolved in 10 mL of hot methanol and 2.2 mL of 48% hydrobromic acid was added. The obtained suspension was stirred, cooled and precipitated solid was filtered off. The cake was washed with cold methanol and air-dried to give 2.7 g of (±)-2-amino-6-propylamino-4,5,6,7-tetrahydrobenzothiazole monohydrobromide with m.p. 236-245° C.
Workup
- temperaturecooled
- customprecipitated solid
- filtrationwas filtered off
- washThe cake was washed with cold methanol
- customair-dried
Sources & evidence
- ORD record
- ord-48c73cce3c344b4faecc611f4e487d12
- Source dataset
- uspto-grants-2004_04
- Patent number
- US06727367B2
Reaction notes
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