Diisopropylamine → Methyl 5-(4-fluorophenyl)-6-hydroxynicotinate
반응식
Br[C:2]1[C:7](=[O:8])[NH:6][CH:5]=[C:4]([C:9]([O:11][CH3:12])=[O:10])[CH:3]=1.[F:13][C:14]1[CH:19]=[CH:18][C:17](B(O)O)=[CH:16][CH:15]=1.[Na+].O.S(C1C=C(P(C2C=CC=C(S([O-])(=O)=O)C=2)C2C=CC=C(S([O-])(=O)=O)C=2)C=CC=1)([O-])(=O)=O.[Na+].[Na+].C(NC(C)C)(C)C>CN(C=O)C.O.C([O-])(=O)C.[Pd+2].C([O-])(=O)C>[F:13][C:14]1[CH:19]=[CH:18][C:17]([C:2]2[C:7](=[O:8])[NH:6][CH:5]=[C:4]([C:9]([O:11][CH3:12])=[O:10])[CH:3]=2)=[CH:16][CH:15]=1참가 물질
반응물 4
생성물 1
시약·촉매·용매 3
반응 조건
- 온도
- 125 °C
실험 절차
To a solution of methyl 5-bromo-6-oxo-1,6-dihydropyridine-3-carboxylate (0.5 g, 2.16 mmol) in DMF (8.1 mL) and water (2.7 mL) were added (4-fluorophenyl)boronic acid (0.38 g, 2.69 mmol), palladium(II)acetate (36.3 mg, 0.16 mmol), tris(3-sulfonatophenyl)phosphine hydrate sodium salt (0.31 g, 0.49 mmol) and diisopropylamine (1.54 mL, 10.77 mmol). The mixture was heated in the microwave reactor for 15 min at 125° C. The mixture was filtered and water was added to the filtrate. The mixture was extracted with ethyl acetate (3×). The combined organic extracts were washed with water (3×), brine, dried over sodium sulfate, filtered and concentrated. Purification by silica gel chromatography (100% dichloromethane→70% dichloromethane/ethyl acetate) gave the title compound (0.35 g). MS 248.1 (M+1).
후처리
- filtrationThe mixture was filtered
- additionwater was added to the filtrate
- extractionThe mixture was extracted with ethyl acetate (3×)
- washThe combined organic extracts were washed with water (3×), brine
- dry with materialdried over sodium sulfate
- filtrationfiltered
- concentrationconcentrated
- customPurification by silica gel chromatography (100% dichloromethane→70% dichloromethane/ethyl acetate)
출처 및 근거
- ORD 기록
- ord-4c9043255e504be898c1ce263e88a52b
- 출처 데이터셋
- uspto-grants-2013_12
- 특허 번호
- US08598209B2
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