4-(4-Phenyl-1,3-thiazol-2-yl)piperidine dihydrochloride → 4-Phenyl-2-(piperidin-4-yl)thiazole
Reaction equation
Cl.Cl.[C:3]1([C:9]2[N:10]=[C:11]([CH:14]3[CH2:19][CH2:18][NH:17][CH2:16][CH2:15]3)[S:12][CH:13]=2)[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1>[OH-].[Na+]>[C:3]1([C:9]2[N:10]=[C:11]([CH:14]3[CH2:19][CH2:18][NH:17][CH2:16][CH2:15]3)[S:12][CH:13]=2)[CH:4]=[CH:5][CH:6]=[CH:7][CH:8]=1Participants
3
Reactant 1
Product 1
Reagents, catalysts & solvents 1
Procedure
To 4-(4-phenyl-1,3-thiazol-2-yl)piperidine dihydrochloride (530 mg, 1.88 mmol) was added an aqueous 1N sodium hydroxide solution (10 ml) and the mixture was extracted with chloroform (50 ml). The extract was dried over anhydrous magnesium sulfate and the solvent was distilled off under reduced pressure to obtain the desired product (461 mg, 100%) as an oil.
Workup
- extractionthe mixture was extracted with chloroform (50 ml)
- dry with materialThe extract was dried over anhydrous magnesium sulfate
- distillationthe solvent was distilled off under reduced pressure
Sources & evidence
- ORD record
- ord-f1e7f5c584574bfd9a6eb52560f02719
- Source dataset
- uspto-grants-2010_12
- Patent number
- US07851473B2
Reaction notes
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