Dimethylformamide → HCID 58046633, compound
Reaction equation
Cl[CH2:2][C:3]([N:5]1[CH2:10][CH2:9][N:8]([CH3:11])[CH2:7][CH2:6]1)=[O:4].O=C1[C:17]2([CH2:22][CH2:21][N:20]([C:23]([O:25][C:26]([CH3:29])([CH3:28])[CH3:27])=[O:24])[CH2:19][CH2:18]2)[N:16]([C:30]2[CH:35]=[CH:34][CH:33]=[CH:32][CH:31]=2)CN1.[C:36](=[O:39])([O-:38])[O-].[K+].[K+].[CH3:42][N:43]([CH3:46])[CH:44]=[O:45]>C(OCC)(=O)C>[CH3:11][N:8]1[CH2:9][CH2:10][N:5]([C:3](=[O:4])[CH2:2][O:38][C:36]([C:30]2[CH:31]=[C:32]([CH:33]=[CH:34][CH:35]=2)[CH2:42][N:43]2[C:44](=[O:45])[C:17]3([CH2:22][CH2:21][N:20]([C:23]([O:25][C:26]([CH3:29])([CH3:28])[CH3:27])=[O:24])[CH2:19][CH2:18]3)[N:16]([C:30]3[CH:35]=[CH:34][CH:33]=[CH:32][CH:31]=3)[CH2:46]2)=[O:39])[CH2:6][CH2:7]1Participants
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 65 °C
Procedure
To a solution of 2-chloro-1-(4-methylpiperazin-1-yl)ethanone in N,N-dimethylformamide (3 mL), was added tert-butyl 4-oxo-1-phenyl-1,3,8-triazaspiro[4.5]decane-8-carboxylate (0.2 g, 0.43 mmol) and potassium carbonate (0.119 g, 0.86 mmol). After stirring at 65° C. for 18 hours, the reaction mixture was diluted with ethyl acetate (25 mL), washed with dilute citric acid, water and brine. The organic phase was dried over MgSO4, filtered and isolated by Biotage flash chromatography (2-20% methanol/dichloromethane) to obtain the title compound (0.16 g, 62%); 1H NMR (DMSO-d6): δ 1.45 (s, 9H), 1.64 (t, 2H, J=12.8 Hz), 2.18 (s, 3H), 2.25-2.45 (m, 6H), 3.41-3.50 (m, 6H), 3.85 (br, 2H), 4.60-4.65 (m, 4H), 5.05 (s, 2H), 6.64-6.69 (m, 2H), 6.76-6.79 (m, 1H), 7.13-7.19 (m, 2H), 7.54-7.60 (m, 2H), 7.91-7.93 (m, 2H); MS for C33H43N5O6 m/z 606.08 (M+H)+.
Workup
- washwashed with dilute citric acid, water and brine
- dry with materialThe organic phase was dried over MgSO4
- filtrationfiltered
- customisolated by Biotage flash chromatography (2-20% methanol/dichloromethane)
Sources & evidence
- ORD record
- ord-025e705f23de4d8b9994c3dae4bfc71d
- Source dataset
- uspto-grants-2014_04
- Patent number
- US08691836B2
Reaction notes
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