Hydrochloric Acid → HCID 86628293, 화합물
반응식
[CH:1]([C:3]1[CH:11]=[CH:10][C:6]([C:7]([OH:9])=O)=[CH:5][C:4]=1[O:12][CH2:13][O:14][CH3:15])=[O:2].CCN=C=NCCCN(C)C.C1C=C2N=NN(O)C2=CC=1.O.[C:38]([NH2:47])([C:41]1[CH:46]=[CH:45][CH:44]=[CH:43][CH:42]=1)([CH3:40])[CH3:39].Cl>CN(C=O)C.O>[CH:1]([C:3]1[CH:11]=[CH:10][C:6]([C:7]([NH:47][C:38]([CH3:40])([C:41]2[CH:46]=[CH:45][CH:44]=[CH:43][CH:42]=2)[CH3:39])=[O:9])=[CH:5][C:4]=1[O:12][CH2:13][O:14][CH3:15])=[O:2]참가 물질
실험 절차
4-Formyl-3-methoxymethoxybenzoic acid (2.57 g, 12.2 mmol) was dissolved in DMF (50 mL), and the solution was added with EDCI (4.68 g, 24.4 mmol), HOBT monohydrate (1.65 g, 12.2 mmol) and cumylamine (4.03 mL, 24.4 mmol), followed by stirring at room temperature for 4 hours. The reaction mixture was added with water (10 mL) and 1 mol/L hydrochloric acid (10 mL) and stirred at room temperature for 1 hour. The reaction mixture was added with water and extracted with ethyl acetate. The organic layer was washed with water and saturated aqueous sodium hydrogencarbonate solution and saturated brine, followed by drying over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure and the residue was purified by flash column chromatography (hexane/ethyl acetate=95/5 to 80/20 to 70/30) to obtain 4-formyl-3-methoxymethoxy-N-(1-methyl-1-phenylethyl)benzamide (3.12 g, yield 78%).
후처리
- stirringstirred at room temperature for 1 hour
- extractionextracted with ethyl acetate
- washThe organic layer was washed with water and saturated aqueous sodium hydrogencarbonate solution and saturated brine
- dry with materialby drying over anhydrous sodium sulfate
- customThe solvent was evaporated under reduced pressure
- customthe residue was purified by flash column chromatography (hexane/ethyl acetate=95/5 to 80/20 to 70/30)
출처 및 근거
- ORD 기록
- ord-3bbf80376b0f4c05ab93e397b1118499
- 출처 데이터셋
- uspto-grants-2010_06
- 특허 번호
- US07745641B2
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