Acetic Acid → 5-Amino-6-((S)-2-imidazol-1-yl-1-phenyl-ethoxy)-3,4-dihydro-2H-naphthalen-1-one
반응식
[N+:1]([C:4]1[C:13]([O:14][C@@H:15]([C:22]2[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=2)[CH2:16][N:17]2[CH:21]=[CH:20][N:19]=[CH:18]2)=[CH:12][CH:11]=[C:10]2[C:5]=1[CH2:6][CH2:7][CH2:8][C:9]2=[O:28])([O-])=O.CO.C(O)(=O)C.C([O-])(O)=O.[Na+]>[Fe].CO.C(Cl)Cl.CCOC(C)=O.O>[NH2:1][C:4]1[C:13]([O:14][C@@H:15]([C:22]2[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=2)[CH2:16][N:17]2[CH:21]=[CH:20][N:19]=[CH:18]2)=[CH:12][CH:11]=[C:10]2[C:5]=1[CH2:6][CH2:7][CH2:8][C:9]2=[O:28]참가 물질
반응물 4
생성물 1
시약·촉매·용매 4
실험 절차
A mixture of 5-nitro-6-((S)-2-imidazol-1-yl-1-phenyl-ethoxy)-3,4-dihydro-2H-naphthalen-1-one (2.05 g, 5.43 mmol), MeOH (135 mL), H2O (30 mL) and glacial acetic acid (3.1 mL, 54 mmol) was treated at reflux with iron powder (3.01 g, 54 mmol). The reaction was monitored by mass spectrometry and was complete in 5 h. The volume of solvent was reduced under reduced pressure. EtOAc and dilute aqueous NaHCO3 were added. A brownish-green emulsion formed which was filtered through Celite. The mixture was extracted with EtOAc. The combined organic layer was washed with dilute aqueous NaHCO3 and brine, dried over Na2SO4, and concentrated under reduced pressure to give a brown solid. Purification by chromatography (EtOAc then 6% MeOH/CH2Cl2) gave the product as a tan solid (1.43 g, 4.12 mmol, 76%). The structure was confirmed by NMR and mass spectrometry. MS m/z 348 (M++H).
후처리
- additionwas treated
- customA brownish-green emulsion formed which
- filtrationwas filtered through Celite
- extractionThe mixture was extracted with EtOAc
- washThe combined organic layer was washed with dilute aqueous NaHCO3 and brine
- dry with materialdried over Na2SO4
- concentrationconcentrated under reduced pressure
- customto give a brown solid
- customPurification by chromatography (EtOAc
출처 및 근거
- ORD 기록
- ord-c76182f548b94a59ac1c9392ce917451
- 출처 데이터셋
- uspto-grants-2005_09
- 특허 번호
- US06943183B2
반응 노트
불러오는 중…