反応式
Br[CH2:2][C:3](=O)[CH:4]([CH3:6])[CH3:5].[NH2:8][C:9](=[S:15])[C:10]([O:12][CH2:13][CH3:14])=[O:11]>C(O)C>[CH:4]([C:3]1[N:8]=[C:9]([C:10]([O:12][CH2:13][CH3:14])=[O:11])[S:15][CH:2]=1)([CH3:6])[CH3:5]参加物
実験手順
1-Bromo-3-methylbutan-2-one (3.72 g) in ethanol (15 mL) was added dropwise over 15 minutes to a refluxing solution of ethyl 2-amino-2-thioxoacetate (3 g) in ethanol (120 mL). The mixture was heated at reflux for 2 hours and then cooled to room temperature. The solvent was evaporated down under reduced pressure to a volume of 30 mL, this solution was added to ice/water (200 mL) and the mixture neutralised by dropwise addition of ‘880’ concentrated aqueous ammonia. The mixture was extracted twice with ethyl acetate, the combined organics were washed with brine, dried over sodium sulphate, filtered and the solvent evaporated under reduced pressure. The crude product was purified by flash silica chromatography eluting with 20% ethyl acetate in isohexane. Pure fractions were evaporated to dryness to afford the subtitled compound. Yield 2.2 g.
後処理
- temperatureThe mixture was heated
- temperatureat reflux for 2 hours
- customThe solvent was evaporated down under reduced pressure to a volume of 30 mL
- additionthis solution was added to ice/water (200 mL)
- additionthe mixture neutralised by dropwise addition of ‘880’ concentrated aqueous ammonia
- extractionThe mixture was extracted twice with ethyl acetate
- washthe combined organics were washed with brine
- dry with materialdried over sodium sulphate
- filtrationfiltered
- customthe solvent evaporated under reduced pressure
- customThe crude product was purified by flash silica chromatography
- washeluting with 20% ethyl acetate in isohexane
- customPure fractions were evaporated to dryness
出典と根拠
- ORDレコード
- ord-58e413c2f5024fc68c8072edb22b80fa
- 出典データセット
- uspto-grants-2014_01
- 特許番号
- US08629271B2
関連ノート
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