Hydrochloric Acid → 7-Amino-8-methylquinoline-3-carbaldehyde
반응식
[CH3:1][C:2]1[C:7]([NH2:8])=[CH:6][CH:5]=[CH:4][C:3]=1[NH2:9].Cl.[C:11](=[O:14])([O-])[O-].[K+].[K+].[CH:17](OC(C)C)([CH3:19])[CH3:18]>C(O)(C)C.C(OCC)(=O)C.O>[NH2:8][C:7]1[C:2]([CH3:1])=[C:3]2[C:4]([CH:18]=[C:17]([CH:11]=[O:14])[CH:19]=[N:9]2)=[CH:5][CH:6]=1참가 물질
실험 절차
A suspension of 2-methyl-1,3-benzenediamine (30.0 g, 246 mmol) and 2-dimethylaminomethylene-1,3-bis(dimethylimmonio)propane bis-tetrafluoroborate (263 g, 737 mmol) in isopropanol (500 ml) was heated under reflux with stirring for 16 hrs. and allowed to cool to room temperature. To the reaction solution was added 1N hydrochloric acid (500 ml). The mixture was stirred at 70° C. for 5 hrs. with heating and allowed to cool to room temperature. The resulting precipitate was collected and washed with water, acetonitrile and isopropyl ether. A suspension of the obtained precipitate (61.6 g) and potassium carbonate (170 g, 1.23 mol) in ethyl acetate (500 ml)-water (500 ml) was vigorously stirred with heating at 90° C. and allowed to cool to room temperature. The organic layer was separated, washed with saturated brine, dried over sodium sulfate and passed through silica gel (100 g) packed in a glass filter. The solvent was evaporated under reduced pressure and the obtained crude product was treated with isopropyl ether to give the title compound (35.4 g) as a powder.
후처리
- temperaturewas heated
- temperatureunder reflux
- stirringThe mixture was stirred at 70° C. for 5 hrs
- temperaturewith heating
- temperatureto cool to room temperature
- customThe resulting precipitate was collected
- washwashed with water, acetonitrile and isopropyl ether
- stirringwas vigorously stirred
- temperaturewith heating at 90° C.
- temperatureto cool to room temperature
- customThe organic layer was separated
- washwashed with saturated brine
- dry with materialdried over sodium sulfate
- filtrationfilter
- customThe solvent was evaporated under reduced pressure
- customthe obtained crude product
출처 및 근거
- ORD 기록
- ord-99095e4ff0ba4959b49c73bcc1599ad2
- 출처 데이터셋
- uspto-grants-2007_02
- 특허 번호
- US07183415B2
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