Sodium Carbonate → Methyl (3R)-3-phthalimido-3-(3,4-dimethoxyphenyl)propionate
Reaction equation
[NH2:1][C@@H:2]([C:8]1[CH:13]=[CH:12][C:11]([O:14][CH3:15])=[C:10]([O:16][CH3:17])[CH:9]=1)[CH2:3][C:4]([O:6][CH3:7])=[O:5].C(=O)([O-])[O-].[Na+].[Na+].C(N1[C:33](=[O:34])[C:32]2=[CH:35][CH:36]=[CH:37][CH:38]=[C:31]2[C:30]1=[O:39])(OCC)=O>>[C:30]1(=[O:39])[N:1]([C@@H:2]([C:8]2[CH:13]=[CH:12][C:11]([O:14][CH3:15])=[C:10]([O:16][CH3:17])[CH:9]=2)[CH2:3][C:4]([O:6][CH3:7])=[O:5])[C:33](=[O:34])[C:32]2=[CH:35][CH:36]=[CH:37][CH:38]=[C:31]12Participants
Procedure
Methyl (3R)-3-amino-3-(3,4-dimethoxyphenyl)propionate (0.25 g, 0.91 mmol), sodium carbonate (0.10 g, 0.91 mmol) and N-carboethoxyphthalimide (0.20 g, 0.91 mmol) were allowed to react according to the procedure of Example 85. Methyl (3R)-3-phthalimido-3-(3,4-dimethoxyphenyl)propionate was obtained as a white powder, 0.29 g (88%); 1H NMR (DMSO-d6, 250 MHz) δ7.87 (br s, 4H, Ar), 6.80-7.10 (m, 3H, Ar), 5.64 (dd, 1H, J1=7 Hz, J2=9 Hz), 3.73 (s, 3H, OCH3), 3.72 (s, 3H, OCH3), 355 (s, 3H, OCH3), 3.30-3.67 (m, 2H); 13C NMR (DMSO-d6) δ170.8, 167.6, 148.6, 148.4, 134.7, 131.1, 131.0, 123.2, 119.2, 111.7, 111.0, 55.5, 51.6, 49.9, 35.6. Anal. Calcd for C20H19NO60.80 H2O. Theoretical C, 62.60; H, 4.99; N, 3.69. Found C, 62.60; H, 4.93; N, 3.69. HPLC 99.9%.
Workup
- customto react
Sources & evidence
- ORD record
- ord-5b84c6d6ba6e45a99103973e6037182f
- Source dataset
- uspto-grants-2001_03
- Patent number
- US06200987B1
Reaction notes
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