Chlorosuccinimide → Ethyl 1-(4-chloromethyl-5-methyl-1,3-thiazol-2-yl)piperidine-4-carboxylate
Reaction equation
[CH3:1][C:2]1[N:3]=[C:4]([N:8]2[CH2:13][CH2:12][CH:11]([C:14]([O:16][CH2:17][CH3:18])=[O:15])[CH2:10][CH2:9]2)[S:5][C:6]=1[CH3:7].[Cl:19]N1C(=O)CCC1=O.C(=O)([O-])O.[Na+]>C(#N)C>[Cl:19][CH2:1][C:2]1[N:3]=[C:4]([N:8]2[CH2:13][CH2:12][CH:11]([C:14]([O:16][CH2:17][CH3:18])=[O:15])[CH2:10][CH2:9]2)[S:5][C:6]=1[CH3:7]Participants
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 0 °C
Procedure
To a mixture of ethyl 1-(4,5-dimethyl-1,3-thiazol-2-yl)piperidine-4-carboxylate (6.51 g), acetonitrile (100 mL) was added N-chlorosuccinimide (3.24 g) at 0° C. The reaction mixture was stirred at 0° C. for 2 hrs. Saturated aqueous sodium hydrogen carbonate was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate and concentrated. The residue was subjected to silica gel column chromatography and eluted with ethyl acetate-hexane (1:3, v/v) to give ethyl 1-(4-chloromethyl-5-methyl-1,3-thiazol-2-yl)piperidine-4-carboxylate as colorless crystals (1.93 g, yield 26%). The crystals were recrystallized from ethyl acetate-hexane. melting point: 76-77° C.
Workup
- extractionthe mixture was extracted with ethyl acetate
- washThe organic layer was washed with saturated brine
- dry with materialdried over anhydrous magnesium sulfate
- concentrationconcentrated
- washeluted with ethyl acetate-hexane (1:3
Sources & evidence
- ORD record
- ord-dd4157df683e4ab19cc4a7f91284c9dc
- Source dataset
- uspto-grants-2008_05
- Patent number
- US07368578B2
Reaction notes
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