HCID 22482739, compound → HCID 5252118, compound
Reaction equation
Cl.[C:2]([C:5]1[CH2:6][CH2:7][NH:8][CH2:9][CH:10]=1)(=[O:4])[NH2:3]>C(=O)([O-])O.[Na+]>[C:2]([C:5]1[CH2:10][CH2:9][NH:8][CH2:7][CH:6]=1)(=[O:4])[NH2:3]Participants
3
Reactant 1
Product 1
Reagents, catalysts & solvents 1
Procedure
4-carbamoyl-1,2,3,6-tetrahydropyridine hydrochloride was dissolved in a saturated aqueous solution of sodium hydrogen carbonate, followed by extraction with chloroform. The organic layer was dried over anhydrous sodium sulfate. After the desiccant was filtered off, the filtrate was concentrated under reduced pressure to yield crystals of free 4-carbamoyl-1,2,3,6-tetrahydropyridine.
Workup
- extractionfollowed by extraction with chloroform
- dry with materialThe organic layer was dried over anhydrous sodium sulfate
- filtrationAfter the desiccant was filtered off
- concentrationthe filtrate was concentrated under reduced pressure
Sources & evidence
- ORD record
- ord-8dc05a1003474a09885a01d63723aa5a
- Source dataset
- uspto-grants-2003_07
- Patent number
- US06600038B1
Reaction notes
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