Hydrochloric Acid → N-(5-Amino-2-hydroxy-2-(4-isopropyl-2-methoxyphenyl)-1,3-dioxo-2,3-dihydro-1H-inden-4-yl)acetamide
반응식
[OH:1][C:2]1([C:20]2[CH:25]=[CH:24][C:23]([CH:26]([CH3:28])[CH3:27])=[CH:22][C:21]=2[O:29][CH3:30])[C:10](=[O:11])[C:9]2[C:4](=[CH:5][CH:6]=[C:7]([N+:16]([O-])=O)[C:8]=2[NH:12][C:13](=[O:15])[CH3:14])[C:3]1=[O:19].Cl.O>C(O)C.[Fe]>[NH2:16][C:7]1[C:8]([NH:12][C:13](=[O:15])[CH3:14])=[C:9]2[C:4](=[CH:5][CH:6]=1)[C:3](=[O:19])[C:2]([OH:1])([C:20]1[CH:25]=[CH:24][C:23]([CH:26]([CH3:27])[CH3:28])=[CH:22][C:21]=1[O:29][CH3:30])[C:10]2=[O:11]참가 물질
6
반응물 3
생성물 1
시약·촉매·용매 2
실험 절차
N-(2-hydroxy-2-(4-isopropyl-2-methoxyphenyl)-5-nitro-1,3-dioxo-2,3-dihydro-1H-inden-4-yl)acetamide (0.10 g, 0.24 mmol) was completely dissolved in anhydrous ethanol (3 ml). This solution was added with iron (0.098 g), conc. HCl (0.05 ml) and water (0.3 ml). The reaction mixture was heated for 2 hrs under reflux. After filtration at high temperature to remove iron, the filtrate was concentrated in a vacuum and purified using column chromatography (ethylacetate 100%) to afford the title compound (90 mg, 98%).
후처리
- temperatureThe reaction mixture was heated for 2 hrs
- temperatureunder reflux
- filtrationAfter filtration at high temperature
- customto remove iron
- concentrationthe filtrate was concentrated in a vacuum
- custompurified
출처 및 근거
- ORD 기록
- ord-96472b29eea344aabaea3251405c53d3
- 출처 데이터셋
- uspto-grants-2016_05
- 특허 번호
- US09346749B2
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