Methanol → HCID 67288093, compound
Reaction equation
[Cl:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][C:11]=1[O:12][C:13]1[CH:18]=[CH:17][C:16]([C:19](=[O:35])[NH:20][C:21]3[N:26]=[C:25]([C:27]4[CH:28]=[N:29][C:30]([O:33][CH3:34])=[CH:31][CH:32]=4)[CH:24]=[CH:23][CH:22]=3)=[CH:15][CH:14]=1)[O:8][CH2:7][CH2:6][CH:5]2[C:36]([OH:38])=[O:37].C[O-].[Na+:41].CO>C1COCC1.CO>[Cl:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][C:11]=1[O:12][C:13]1[CH:18]=[CH:17][C:16]([C:19](=[O:35])[NH:20][C:21]3[N:26]=[C:25]([C:27]4[CH:28]=[N:29][C:30]([O:33][CH3:34])=[CH:31][CH:32]=4)[CH:24]=[CH:23][CH:22]=3)=[CH:15][CH:14]=1)[O:8][CH2:7][CH2:6][CH:5]2[C:36]([O-:38])=[O:37].[Na+:41]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
To a solution of 6-chloro-7-(4-(6′-methoxy-2,3′-bipyridin-6-ylcarbamoyl)phenoxy)chroman-4-carboxylic acid (0.080 g, 0.150 mmol) in 1:1 THF/methanol (2 ml) was added a 0.5 M solution of sodium methoxide in methanol (0.301 ml, 0.150 mmol), and the reaction was stirred for 2 hours, then concentrated to yield the desired compound (0.080 g, 0.144 mmol, 96.0% yield). MS (apci) m/z=532.2 (M-Na+2H).
Workup
- concentrationconcentrated
Sources & evidence
- ORD record
- ord-60e5e39f84b341f5aeda74dab66936d7
- Source dataset
- uspto-grants-2014_07
- Patent number
- US08785445B2
Reaction notes
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