Methylamine → Tert-butyl 8-(methylamino)-2-azaspiro[4.5]decane-2-carboxylate
Reaction equation
CN.O=[C:4]1[CH2:20][CH2:19][C:7]2([CH2:11][N:10]([C:12]([O:14][C:15]([CH3:18])([CH3:17])[CH3:16])=[O:13])[CH2:9][CH2:8]2)[CH2:6][CH2:5]1.[BH3-][C:22]#[N:23].[Na+]>>[CH3:22][NH:23][CH:4]1[CH2:20][CH2:19][C:7]2([CH2:11][N:10]([C:12]([O:14][C:15]([CH3:18])([CH3:17])[CH3:16])=[O:13])[CH2:9][CH2:8]2)[CH2:6][CH2:5]1Participants
4
Procedure
To a solution of methylamine (33% [w/w] in EtOH, 7.42 g, 79.0 mmol) was added tert-butyl 8-oxo-2-azaspiro[4.5]decane-2-carboxylate (4 g, 15.80 mmol), the reaction mixture was stirred at rt overnight. To the mixture was added NaBH3CN (2.98 g, 47.4 mmol), and the reaction mixture was stirred at rt for another 2 h and concentrated in vacuo. The residue was diluted with H2O (50 mL) and the resulting mixture was extracted with DCM (80 mL×3). The combined organic phases were washed with brine (100 mL), dried over Na2SO4, filtered and concentrated in vacuo. The residue was purified by silica gel column chromatography (DCM/MeOH (v/v)=10/1) to give the product as yellow oil (3.2 g, 75.7%).
Workup
- stirringthe reaction mixture was stirred at rt for another 2 h
- concentrationconcentrated in vacuo
- additionThe residue was diluted with H2O (50 mL)
- extractionthe resulting mixture was extracted with DCM (80 mL×3)
- washThe combined organic phases were washed with brine (100 mL)
- dry with materialdried over Na2SO4
- filtrationfiltered
- concentrationconcentrated in vacuo
- customThe residue was purified by silica gel column chromatography (DCM/MeOH (v/v)=10/1)
Sources & evidence
- ORD record
- ord-a4732ffe5fd04d42b3b0175dc671f003
- Source dataset
- uspto-grants-2016_08
- Patent number
- US09403801B2
Reaction notes
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