Methyl (E)-4-(4-aminophenyl)-3-butenoate → HCID 178500100、化合物
反応式
[NH2:1][C:2]1[CH:7]=[CH:6][C:5](/[CH:8]=[CH:9]/[CH2:10][C:11]([O:13][CH3:14])=[O:12])=[CH:4][CH:3]=1.CS[C:17]1[NH:18][CH:19]=[CH:20][C:21](=[O:23])[N:22]=1>>[O:23]=[C:21]1[CH:20]=[CH:19][NH:18][C:17]([NH:1][C:2]2[CH:3]=[CH:4][C:5](/[CH:8]=[CH:9]/[CH2:10][C:11]([O:13][CH3:14])=[O:12])=[CH:6][CH:7]=2)=[N:22]1参加物
3
実験手順
A mixture comprising 3.00 g of methyl (E)-4-(4-aminophenyl)-3-butenoate and 2.34 g of 2-methylthio-1,4-dihydro-4-oxopyrimidine was stirred at 150° to 160° C. for 20 minutes. The reaction mixture was purified by silica gel column chromatography [solvent: dichloromethane/methanol (30:1)] to obtain 1.58 g of the title compound as a light brown powder (yield: 35%).
後処理
- customThe reaction mixture was purified by silica gel column chromatography [solvent: dichloromethane/methanol (30:1)]
出典と根拠
- ORDレコード
- ord-663d8520e9a2497eb30e6bd546f3dc83
- 出典データセット
- uspto-grants-1994_03
- 特許番号
- US05292770
反応ノート
読み込み中…