反応式
Cl.C(O[N:5]=[CH:6][C:7]1[CH:17]=[CH:16][C:10]([C:11]([O:13][CH2:14][CH3:15])=[O:12])=[CH:9][CH:8]=1)C.[CH2:18](N)[CH2:19][NH2:20]>C(O)C>[NH:20]1[CH2:19][CH2:18][N:5]=[C:6]1[C:7]1[CH:8]=[CH:9][C:10]([C:11]([O:13][CH2:14][CH3:15])=[O:12])=[CH:16][CH:17]=1参加物
実験手順
The resulting ethyl 4-[1-(ethoxy)iminomethyl]benzoate hydrochloride (2.00 g) was dissolved in ethanol (30 ml). Under ice cooling, ethylenediamine (0.52 ml) was added to the resulting solution, followed by heating to room temperature. The reaction mixture was stirred overnight. To the residue obtained by distilling off the solvent under reduced pressure, dilute hydrochloric acid was added to make it acidic, followed by concentration again. The residue was purified by chromatography through a synthetic adsorbent (“Diaion HP-20”, trade name; water˜50% acetonitrile-water). Solution of hydochloride in ethanol was added to the resulting fraction and the mixture was concentrated. Colorless crystalline powder precipitated by the addition of tetrahydrofuran was collected by filtration and dried, whereby the title compound (1.63 g, 19%) was obtained.
後処理
- customTo the residue obtained
- distillationby distilling off the solvent under reduced pressure, dilute hydrochloric acid
- additionwas added
- concentrationfollowed by concentration again
- customThe residue was purified by chromatography through a synthetic adsorbent (“Diaion HP-20”, trade name; water˜50% acetonitrile-water)
- additionSolution of hydochloride in ethanol was added to the resulting fraction
- concentrationthe mixture was concentrated
- customColorless crystalline powder precipitated by the addition of tetrahydrofuran
- filtrationwas collected by filtration
- customdried
出典と根拠
- ORDレコード
- ord-ff087d32c8ed47359c453f9c1a4f1ce5
- 出典データセット
- uspto-grants-2004_06
- 特許番号
- US06747023B1
関連ノート
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