Sulfuric acid magnesium salt (1:1) → 3-(4-Chlorophenyl)-2-isopropyl-7H-pyrano[2,3-e]indazol-4-one
反応式
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[C:17](=[O:18])[C:16]3[C:11](=[C:12]([CH:32]=O)[C:13](OS(C4C(C)=CC(C)=CC=4C)(=O)=O)=[CH:14][CH:15]=3)[O:10][C:9]=2[CH:34]([CH3:36])[CH3:35])=[CH:4][CH:3]=1.S([O-])([O-])(=O)=O.[Mg+2].C([O-])(=O)C.[NH4+:47].O.[NH2:49]N>C(O)C>[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[C:17](=[O:18])[C:16]3[C:11]([O:10][C:9]=2[CH:34]([CH3:36])[CH3:35])=[C:12]2[C:13](=[CH:14][CH:15]=3)[NH:49][N:47]=[CH:32]2)=[CH:4][CH:3]=1参加物
反応条件
- 温度
- 145 °C
実験手順
To a suspension of 2,4,6-trimethylbenzenesulfonic acid 3-(4-chlorophenyl)-8-formyl-2-isopropyl-4-oxo-4H-chromen-7-yl ester (391 mg, 0.745 mmol), magnesium sulphate (450 mg, 3.72 mmol) and ammonium acetate (230 mg, 2.98 mmol) in ethanol (15 ml) in a 20 ml microwave tube is added hydrazine hydrate (0.93 ml, 2.98 mmol). The tube is sealed and heated at 145° C. for ca. 80 min. The mixture is cooled to room temperature, and the volatiles are evaporated under reduced pressure. The residue is dissolved in dry pyridine (14 ml), the solution is transferred to a 20 ml microwave tube, the tube is sealed, and the mixture is heated at 190° C. for 100 min. The mixture is cooled and evaporated to dryness. The residue is purified by chromatography on silica gel using cyclohexane/ethyl acetate (6:1) as eluant.
後処理
- customThe tube is sealed
- temperatureThe mixture is cooled to room temperature
- customthe volatiles are evaporated under reduced pressure
- dissolutionThe residue is dissolved in dry pyridine (14 ml)
- customthe solution is transferred to a 20 ml microwave tube
- customthe tube is sealed
- temperaturethe mixture is heated at 190° C. for 100 min
- temperatureThe mixture is cooled
- customevaporated to dryness
- customThe residue is purified by chromatography on silica gel
出典と根拠
- ORDレコード
- ord-1b847f9f58a34d30a91eb189bd764274
- 出典データセット
- uspto-grants-2010_06
- 特許番号
- US07732435B2
反応ノート
読み込み中…