Pyridine → 7-Methanesulfonyl-amino-benzofuran-4-carboxylic acid methyl ester
Reaction equation
[CH3:1][O:2][C:3]([C:5]1[CH:6]=[CH:7][C:8](N)=[C:9]2[O:13][CH:12]=[CH:11][C:10]=12)=[O:4].[N:15]1C=CC=CC=1.[CH3:21][S:22](Cl)(=[O:24])=[O:23]>ClCCl>[CH3:1][O:2][C:3]([C:5]1[CH:6]=[CH:7][C:8]([S:22]([CH3:21])(=[O:24])=[O:23])=[C:9]2[O:13][C:12]([NH2:15])=[CH:11][C:10]=12)=[O:4]Participants
Procedure
To a solution of 7-amino-benzofuran-4-carboxylic acid methyl ester (6.14 g, 32.1 mmol) and pyridine (13.69 g, 173 mmole) in dichloromethane (100 mL) was added methanesulfonyl chloride (2.8 mL, 36.2 mmol). The reaction mixture was stirred at room temperature under nitrogen for 72 hours. The solvent was removed under reduced pressure and the residue partitioned between dichloromethane and 1 N hydrochloric acid. The organic extract was dried (anhydrous sodium sulfate) and concentrated. The residue was purified by flash column chromatography over silica gel eluting with 20 to 30% ethyl acetate in hexane to give 7-methanesulfonyl-amino-benzofuran-4-carboxylic acid methyl ester (7.73 g, 89%) as a solid. 1H NMR (CDCl3) δ: 3.15 (s, 3H), 3.98 (s, 3H), 7.43 (d, 1H, J=2.2 Hz), 7.50 (d, 1H, J=8.4 Hz), 7.74 (d, 1H, J=2.1 Hz), 8.00 (d, 1H, J=8.3 Hz).
Workup
- customThe solvent was removed under reduced pressure
- customthe residue partitioned between dichloromethane and 1 N hydrochloric acid
- extractionThe organic extract
- dry with materialwas dried (anhydrous sodium sulfate)
- concentrationconcentrated
- customThe residue was purified by flash column chromatography over silica gel eluting with 20 to 30% ethyl acetate in hexane
Sources & evidence
- ORD record
- ord-7177f770167c4b3c8875fd7d2a187cd1
- Source dataset
- uspto-grants-2004_06
- Patent number
- US06756395B2
Reaction notes
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