反応式
[CH2:1]([O:7][C:8]1[CH:26]=[CH:25][C:11]([C:12]([NH:14][C:15]2[CH:24]=[CH:23][C:18]([C:19](OC)=[O:20])=[CH:17][CH:16]=2)=[O:13])=[CH:10][CH:9]=1)[CH2:2][CH2:3][CH2:4][CH2:5][CH3:6].O.[NH2:28][NH2:29]>CCO>[CH2:1]([O:7][C:8]1[CH:26]=[CH:25][C:11]([C:12]([NH:14][C:15]2[CH:24]=[CH:23][C:18]([C:19]([NH:28][NH2:29])=[O:20])=[CH:17][CH:16]=2)=[O:13])=[CH:10][CH:9]=1)[CH2:2][CH2:3][CH2:4][CH2:5][CH3:6]参加物
4
実験手順
To a suspension of methyl 4-{[4-(hexyloxy)benzoyl]amino}benzoate (856 mg, 2.41 mmol) in EtOH (10 mL) was added hydrazine hydrate (1.8 mL). After stirring for 15 h at reflux, the reaction mixture was cooled to rt and a white solid precipitated out. Filtration, washing with EtOH (1×2 mL) and water (2×2 mL), and drying under vacuo at rt for 72 hrs gave 681 mg of the title compound (80%) as a white solid in 99.7% purity by HPLC (MaxPlot detection between 230 and 400 nm).
後処理
- temperatureat reflux
- customa white solid precipitated out
- filtrationFiltration
- washwashing with EtOH (1×2 mL) and water (2×2 mL)
- customdrying under vacuo at rt for 72 hrs
出典と根拠
- ORDレコード
- ord-118a8f56c91c49d78e640cc15d227d8a
- 出典データセット
- uspto-grants-2010_04
- 特許番号
- US07696231B2
関連ノート
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