Hydrochloric Acid → HCID 62480333, compound
Reaction equation
[CH3:1][CH:2]1[CH2:7][NH:6][CH2:5][CH2:4][NH:3]1.Br[C:9]1[S:10][CH:11]=[CH:12][N:13]=1.Cl>>[CH3:1][CH:2]1[NH:3][CH2:4][CH2:5][N:6]([C:9]2[S:10][CH:11]=[CH:12][N:13]=2)[CH2:7]1Participants
4
Procedure
30.06 g (300.0 mmol) of 2-methylpiperazine were combined with 4.51 ml (50.0 mmol) of 2-bromothiazole. This mixture was fused and refluxed 5 min. The reaction mixture was cooled and taken up in 10% strength hydrochloric acid and washed with EA. The aqueous phase was set to pH>12 with a 10% strength aq. NaOH solution and then extracted with EA. The organic phase was dried over MgSO4 and conc. in vacuo. There were obtained 8.26 g (45.1 mmol, 90%) of 3-methyl-1-thiazol-2-ylpiperazine.
Workup
- temperaturerefluxed 5 min
- temperatureThe reaction mixture was cooled
- washwashed with EA
- extractionextracted with EA
- dry with materialThe organic phase was dried over MgSO4 and conc. in vacuo
Sources & evidence
- ORD record
- ord-7d1e0e53bed2463cb28340dc70e0db85
- Source dataset
- uspto-grants-2007_11
- Patent number
- US07300939B2
Reaction notes
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