Dimethylamine → N,N-dimethyl-1-t-butoxycarbonyl-4-phenylpiperidine-4-carboxamide
Reaction equation
C1CN([P+](ON2N=N[C:20]3[CH:21]=[CH:22][CH:23]=[CH:24][C:19]2=3)(N2CCCC2)N2CCCC2)CC1.F[P-](F)(F)(F)(F)F.CN(C=[O:38])C.[CH3:39][N:40]1[CH2:45][CH2:44]O[CH2:42][CH2:41]1.[NH:46]([CH3:48])[CH3:47].[CH3:49][C:50]([O:53]C)([CH3:52])[CH3:51].[CH3:55][CH2:56][O:57]C(C)=O>CN(C1C=CN=CC=1)C>[C:50]([O:53][C:39]([N:40]1[CH2:41][CH2:42][C:55]([C:56](=[O:57])[N:46]([CH3:48])[CH3:47])([C:19]2[CH:20]=[CH:21][CH:22]=[CH:23][CH:24]=2)[CH2:44][CH2:45]1)=[O:38])([CH3:49])([CH3:51])[CH3:52]Participants
Conditions
- Temperature
- 20 °C
Procedure
A 250 mL round-bottom flask was charged with acid (6.1 g; 20 mmol), PyBOP (10.4 g; 20 mmol), DMF (100 mL) and NMM (4.4 mL; 40 mmol). The reaction mixture was stirred at 20° C. for 15 min and then DMAP (240 mg; 2.0 mmol) and Me2NH (12.0 mL; 60.0 mmol) was added. The reaction mixture was stirred at 20° C. for 12 h. The reaction mixture was diluted with 1:1 MTBE/EtOAc (250 mL). The organic was washed with H2O (250 mL), saturated NaCl (250 mL), dried with MgSO4, filtered and concentrated in vacuo. The crude material was purified by flash chromatography (silica gel hexanes/THF 3:1) to yield pure product (6.0 g; 90% yield). 1H-NMR (300 MHz) δ (ppm) 7.20-7.40 (m; 5H), 3.98 (d; 2H); 3.23 (t; 2H); 2.40-3.00 (bs; 6H); 2.35 (d; 2H); 1.90 (t; 2H); 1.40 (s; 9H). 13C-NMR (300 MHz) δ (ppm) 174.1; 155.3; 145.0; 129.3; 128.8; 127.0; 125.2; 79.6; 49.8; 41.6; 38.0; 35.6; 28.7.
Workup
- stirringThe reaction mixture was stirred at 20° C. for 12 h
- washThe organic was washed with H2O (250 mL), saturated NaCl (250 mL)
- dry with materialdried with MgSO4
- filtrationfiltered
- concentrationconcentrated in vacuo
- customThe crude material was purified by flash chromatography (silica gel hexanes/THF 3:1)
- customto yield pure product (6.0 g; 90% yield)
Sources & evidence
- ORD record
- ord-bff3c40f1d294b0ba8b960b8440783e3
- Source dataset
- uspto-grants-2003_12
- Patent number
- US06656953B2
Reaction notes
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