Water → cis-4-Azidomethyl-1-tert-butoxycarbonyl-3-methoxypiperidine
Reaction equation
[H-].[Na+].[N:3]([CH2:6][C@H:7]1[CH2:12][CH2:11][N:10]([C:13]([O:15][C:16]([CH3:19])([CH3:18])[CH3:17])=[O:14])[CH2:9][C@H:8]1[OH:20])=[N+:4]=[N-:5].[CH3:21]I.O>CN(C)C=O>[N:3]([CH2:6][C@H:7]1[CH2:12][CH2:11][N:10]([C:13]([O:15][C:16]([CH3:17])([CH3:19])[CH3:18])=[O:14])[CH2:9][C@H:8]1[O:20][CH3:21])=[N+:4]=[N-:5]Participants
Procedure
To a solution of 60% sodium hydride (0.58 g) in dimethylformamide (10 ml) was added dropwise a solution of cis-4-azidomethyl-1-tert-butoxycarbonyl-3-hydroxypiperidine (3.4 g) in dimethylformamide (50 ml), and the resulting mixture was stirred at room temperature for 1 hr. Methyl iodide (1.24 ml) was added to the mixture with stirring, and the resulting mixture was stirred at room temperature for 15 hr. Water was added to the reaction mixture and the mixture was extracted with chloroform. The organic layer was washed with brine and dried. The solvent was evaporated under reduced pressure and the residue was purified by silica gel column chromatography (chloroform) to give 1.5 g of cis-4-azidomethyl-1-tert-butoxycarbonyl-3-methoxypiperidine.
Workup
- stirringwith stirring
- stirringthe resulting mixture was stirred at room temperature for 15 hr
- extractionthe mixture was extracted with chloroform
- washThe organic layer was washed with brine
- customdried
- customThe solvent was evaporated under reduced pressure
- customthe residue was purified by silica gel column chromatography (chloroform)
Sources & evidence
- ORD record
- ord-c09afe9b25b3429698b8d2d347524c88
- Source dataset
- uspto-grants-1999_01
- Patent number
- US05864039
Reaction notes
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