반응식
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]=1참가 물질
실험 절차
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.
후처리
- 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
출처 및 근거
- ORD 기록
- ord-ff087d32c8ed47359c453f9c1a4f1ce5
- 출처 데이터셋
- uspto-grants-2004_06
- 특허 번호
- US06747023B1
연결된 노트
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