反応式
[H-].[Na+].C(S)C.[NH2:6][C:7]1[C:15]([Cl:16])=[CH:14][C:10]([C:11]([OH:13])=[O:12])=[C:9]([O:17]C)[CH:8]=1>CN(C)C=O>[NH2:6][C:7]1[C:15]([Cl:16])=[CH:14][C:10]([C:11]([OH:13])=[O:12])=[C:9]([OH:17])[CH:8]=1参加物
反応条件
- 温度
- 25 °C
実験手順
A cooled (5° C.) suspension of 60% sodium hydride oil dispersion (20.0 g, 0.50 mole) in anhydrous dimethylformamide (300 ml) under nitrogen was treated dropwise with ethyl mercaptan (18.7 g, 0.3 mole) while maintaining the reaction temperature below 15° C. The solution was stirred for 15 minutes at 25° C., cooled (5° C.), and treated in small portions with 4-amino-5-chloro-2-methoxybenzoic acid (40.33 g, 0.2 mole). The mixture was heated to 105°±5° C. for 4 hours, cooled, concentrated in vacuo to remove most of the dimethylformamide, then diluted with water (500 ml). The aqueous solution was extracted with methylene chloride (2×150 ml), then with ether (150 ml), acidified with concentrated HCl (55 ml), filtered, and the filter cake was washed with water and dried in vacuo in the presence of Drierite to provide a crude product. The product was recrystallized from tetrahydrofuran/hexane to yield 31.3 g (83%) of white solid, mp 192° C.
後処理
- temperatureA cooled
- temperaturewhile maintaining the reaction temperature below 15° C
- temperaturecooled (5° C.)
- temperatureThe mixture was heated to 105°±5° C. for 4 hours
- temperaturecooled
- concentrationconcentrated in vacuo
- customto remove most of the dimethylformamide
- additiondiluted with water (500 ml)
- extractionThe aqueous solution was extracted with methylene chloride (2×150 ml)
- filtrationfiltered
- washthe filter cake was washed with water
- dry with materialdried in vacuo in the presence of Drierite
- customto provide a crude product
- customThe product was recrystallized from tetrahydrofuran/hexane
出典と根拠
- ORDレコード
- ord-7efec71635e9487ead43743c726bc72a
- 出典データセット
- uspto-grants-1993_12
- 特許番号
- US05273972
関連ノート
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