Hydrazine → 1-Amino-3-methoxy-1H-pyrrole-2,4-dicarboxylic acid diethyl ester
反応式
[CH2:1]([O:3][C:4]([C:6]1[N:7]([N:18]2C(=O)C3C(=CC=CC=3)C2=O)[CH:8]=[C:9]([C:13]([O:15][CH2:16][CH3:17])=[O:14])[C:10]=1[O:11][CH3:12])=[O:5])[CH3:2].NN>CCO>[CH2:1]([O:3][C:4]([C:6]1[N:7]([NH2:18])[CH:8]=[C:9]([C:13]([O:15][CH2:16][CH3:17])=[O:14])[C:10]=1[O:11][CH3:12])=[O:5])[CH3:2]参加物
4
実験手順
A mixture of 393D (0.58 g, 1.58 mmol) and NH2NH2 (60 μl, 2.21 mmol) in EtOH (5 ml) was stirred at rt overnight, filtered through Celite, the filtrate was concentrated and the residue was purified by silica gel flash column chromatography to give 393E (0.30 g, 75%) (0%-5% EtOAc—CH2Cl2).
後処理
- filtrationfiltered through Celite
- concentrationthe filtrate was concentrated
- customthe residue was purified by silica gel flash column chromatography
出典と根拠
- ORDレコード
- ord-4f3ffa5678524a1a8aa0ce1e435ed189
- 出典データセット
- uspto-grants-2006_04
- 特許番号
- US07030112B2
反応ノート
読み込み中…