반응식
[CH3:1][C:2]([CH3:12])([O:4][C:5]([NH:7][CH2:8][C:9]([OH:11])=O)=[O:6])[CH3:3].[CH:13]1([N:19]=C=NC2CCCCC2)CCCC[CH2:14]1.[C:28]1([CH2:34][O:35][C:36]2[CH:41]=[CH:40][C:39](CCN)=[CH:38][CH:37]=2)[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=1>O1CCCC1>[C:28]1([CH2:34][O:35][C:36]2[CH:37]=[CH:38][CH:39]=[CH:40][C:41]=2[CH2:14][CH2:13][NH:19][C:9](=[O:11])[CH2:8][NH:7][C:5]([O:4][C:2]([CH3:1])([CH3:3])[CH3:12])=[O:6])[CH:29]=[CH:30][CH:31]=[CH:32][CH:33]=1참가 물질
실험 절차
N-(1,1-Dimethylethoxycarbonyl)glycine N-(2-(4-phenylmethoxy)phenyl)ethyl)amide. N-(1,1-Dimethylethoxycarbonyl)glycine (850 mg, 4.85 mmol) was stirred with dicyclohexylcarbodiimide (1.00 g, 4.85 mmol) and 2-(4-(phenylmethoxy)phenyl)ethylamine (Intermediate C) (1.00 g, 4.4 mmol) in dry tetrahydrofuran (30 mL) for 16 h. The suspension was filtered and the solvent was evaporated from the filtrate under reduced pressure. The residue was dissolved in ethyl acetate and was washed with aqueous sulphuric acid (10%) and with saturated brine. The solution was dried with anhydrous magnesium sulphate and the solvent was evaporated under reduced pressure to give N-(1,1dimethylethoxycarbonyl)glycine N-(2-(-(phenylmethoxy)phenyl)ethyl)amide (1.65 g, 98%).
후처리
- filtrationThe suspension was filtered
- customthe solvent was evaporated from the filtrate under reduced pressure
- dissolutionThe residue was dissolved in ethyl acetate
- washwas washed with aqueous sulphuric acid (10%) and with saturated brine
- dry with materialThe solution was dried with anhydrous magnesium sulphate
- customthe solvent was evaporated under reduced pressure
출처 및 근거
- ORD 기록
- ord-6078d91084014e80b9e9af5fb94aaee3
- 출처 데이터셋
- uspto-grants-1997_04
- 특허 번호
- US05618528
연결된 노트
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