Acetic Acid → 4-[(3-ethoxy-4-methoxybenzylidene)amino]-3-(2-fluorobenzylsulfanyl)-6-methyl-4H-1,2,4-triazin-5-one
反応式
[CH2:1]([O:3][C:4]1[CH:5]=[C:6]([CH:9]=[CH:10][C:11]=1[O:12][CH3:13])[CH:7]=O)[CH3:2].C(O)(=O)C.[NH2:18][N:19]1[C:24](=[O:25])[C:23]([CH3:26])=[N:22][N:21]=[C:20]1[S:27][CH2:28][C:29]1[CH:34]=[CH:33][CH:32]=[CH:31][C:30]=1[F:35]>C(O)C>[CH2:1]([O:3][C:4]1[CH:5]=[C:6]([CH:9]=[CH:10][C:11]=1[O:12][CH3:13])[CH:7]=[N:18][N:19]1[C:24](=[O:25])[C:23]([CH3:26])=[N:22][N:21]=[C:20]1[S:27][CH2:28][C:29]1[CH:34]=[CH:33][CH:32]=[CH:31][C:30]=1[F:35])[CH3:2]参加物
5
反応条件
- 温度
- 65 °C
実験手順
0.054 g of 3-ethoxy-4-methoxybenzaldehyde and 0.017 ml of acetic acid were added to a solution of 0.080 g of 4-amino-3-(2-fluorobenzylsulfanyl)-6-methyl-4H-1,2,4-triazin-5-one in 4 ml of ethanol, and the mixture was stirred at 65° C. The resultant precipitate was filtered off with suction, giving 4-[(3-ethoxy-4-methoxybenzylidene)amino]-3-(2-fluorobenzylsulfanyl)-6-methyl-4H-1,2,4-triazin-5-one.
後処理
- filtrationThe resultant precipitate was filtered off with suction
出典と根拠
- ORDレコード
- ord-1819011266ed44bbb0e0ad592c19e685
- 出典データセット
- uspto-grants-2009_02
- 特許番号
- US07485639B2
反応ノート
読み込み中…