反応式
[N:1]1[CH:6]=[CH:5][C:4]([C:7]([OH:9])=[O:8])=[CH:3][N:2]=1.S(=O)(=O)(O)O.[CH3:15]O>>[N:1]1[CH:6]=[CH:5][C:4]([C:7]([O:9][CH3:15])=[O:8])=[CH:3][N:2]=1参加物
実験手順
To a solution of pyridazine-4-carboxylic acid (Aldrich, 5.0 g, 40.3 mmol) in methanol (anhydrous, Aldrich, 100 mL) was added sulfuric acid (concentrated, Aldrich, 2 mL). The reaction mixture was then heated to reflux and stirred for 16 hours. The volatiles were removed under reduced pressure. The residue was basified to pH=8-9 with saturated sodium carbonate (20 mL) and then extracted with EtOAc (3×100 mL). The combined extracts were washed with brine (2×20 mL) and dried over magnesium sulfate. The drying agent was filtered off and the organic solution was concentrated and dried to give the titled compound. 1H NMR (300 MHz, DMSO-d6) δ 3.34 (s, 3 H), 8.10 (dd, J=5.2, 2.4 Hz, 1 H), 9.52 (dd, J=5.2, 1.2 Hz, 1 H), 9.58 (dd, J=2.2, 1.4 Hz, 1 H) ppm; MS (DCI/NH3) m/z 139 (M+H)+.
後処理
- temperatureThe reaction mixture was then heated
- temperatureto reflux
- customThe volatiles were removed under reduced pressure
- extractionextracted with EtOAc (3×100 mL)
- washThe combined extracts were washed with brine (2×20 mL)
- dry with materialdried over magnesium sulfate
- filtrationThe drying agent was filtered off
- concentrationthe organic solution was concentrated
- customdried
出典と根拠
- ORDレコード
- ord-f2a44273635e4411b45c734350ab7dc4
- 出典データセット
- uspto-grants-2013_07
- 特許番号
- US08486979B2
関連ノート
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