Ethyl bromopyruvate → Ethyl 2-(3-hydroxy-4-methoxyanilino)-1,3-thiazole-4-carboxylate
反応式
[OH:1][C:2]1[CH:3]=[C:4]([NH:10][C:11]([NH2:13])=[S:12])[CH:5]=[CH:6][C:7]=1[O:8][CH3:9].Br[CH2:15][C:16](=O)[C:17]([O:19][CH2:20][CH3:21])=[O:18]>CN(C=O)C>[OH:1][C:2]1[CH:3]=[C:4]([NH:10][C:11]2[S:12][CH:15]=[C:16]([C:17]([O:19][CH2:20][CH3:21])=[O:18])[N:13]=2)[CH:5]=[CH:6][C:7]=1[O:8][CH3:9]参加物
4
実験手順
Following the general procedure for the synthesis of derivatives 6 and 7, a solution of 1-(3-hydroxy-4-methoxyphenyl)thiourea (150 mg, 0.76 mmol) and ethyl 3-bromopyruvate (0.095 mL, 0.76 mmol) in dry DMF (3.0 mL) was heated at 60° C. for 6 h. The title compound was obtained after purification by flash chromatography on silica gel (hexane:EtOAc 6/4) in 63% yield (139 mg).
後処理
- customfor the synthesis of derivatives 6 and 7
出典と根拠
- ORDレコード
- ord-4d91efbfd2c3430589f6bd4a878bd3b6
- 出典データセット
- uspto-grants-2015_04
- 特許番号
- US09018209B2
反応ノート
読み込み中…