Methanol → HCID 73855136, compound
Reaction equation
[CH2:1]([N:8]1[C:12](=[O:13])[C:11](=[C:14]2[N:18]([CH3:19])[C:17]3[CH:20]=[CH:21][CH:22]=[CH:23][C:16]=3[S:15]2)[S:10][C:9]1=[N:24][C:25]1[CH:26]=[C:27]([NH:34][C:35]([CH2:37][O:38]C(=O)C)=[O:36])[CH:28]=[CH:29][C:30]=1[NH:31][CH2:32][CH3:33])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.CO.O.C(=O)([O-])[O-].[K+].[K+]>C(Cl)(Cl)Cl>[CH2:1]([N:8]1[C:12](=[O:13])[C:11](=[C:14]2[N:18]([CH3:19])[C:17]3[CH:20]=[CH:21][CH:22]=[CH:23][C:16]=3[S:15]2)[S:10][C:9]1=[N:24][C:25]1[CH:26]=[C:27]([NH:34][C:35](=[O:36])[CH2:37][OH:38])[CH:28]=[CH:29][C:30]=1[NH:31][CH2:32][CH3:33])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1Participants
6
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Procedure
To a 50 mL flask was added the product of Example 157 (0.19 g, 0.32 mmol), CHCl3 (5 mL), MeOH (10 mL), water (2 mL), and potassium carbonate (0.22 g, 1.6 mmol). After 4 h the reaction mixture was diluted with CHCl3 (40 mL), and the organic phase was partitioned, washed with water (20 mL), dried over Na2SO4, filtered, and concentrated under reduced pressure. The crude sample was chromatographed (silica gel, 0-10% MeOH/DCM) to afford the title compound (37 mg, 21%). 1H-NMR (CDCl3): δ 8.14 (1H, s), 7.42-7.48 (3H, m), 7.27-7.33 (5H, m), 7.15 (1H, t), 7.09 (1H, dd), 6.99 (1H, d), 6.56 (1H, d), 5.15 (2H, s), 4.14 (2H, s), 3.71 (3H, s), 2.95 (2H, q), 0.99 (3H, t); MS(ESI): 546 (MH+).
Workup
- customthe organic phase was partitioned
- washwashed with water (20 mL)
- dry with materialdried over Na2SO4
- filtrationfiltered
- concentrationconcentrated under reduced pressure
- customThe crude sample was chromatographed (silica gel, 0-10% MeOH/DCM)
Sources & evidence
- ORD record
- ord-cb158f8d6e3c4a76b037f9d3f10a8751
- Source dataset
- uspto-grants-2004_02
- Patent number
- US06696473B2
Reaction notes
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