Hydrochloric Acid → 4-Hydroxy-1-(4-(methylsulfonyl)phenyl)-6-oxo-1,6-dihydropyridine-3-carbonitrile
반응식
[OH:1][C:2]1[C:3]([C:9]#[N:10])=[CH:4][NH:5][C:6](=[O:8])[CH:7]=1.Br[C:12]1[CH:17]=[CH:16][C:15]([S:18]([CH3:21])(=[O:20])=[O:19])=[CH:14][CH:13]=1.COC1C2C(=C3C(=CC=2)C(OC)=CC=N3)N=CC=1.C(=O)([O-])[O-].[K+].[K+].Cl>CS(C)=O.[Cu]I.O>[OH:1][C:2]1[C:3]([C:9]#[N:10])=[CH:4][N:5]([C:12]2[CH:17]=[CH:16][C:15]([S:18]([CH3:21])(=[O:20])=[O:19])=[CH:14][CH:13]=2)[C:6](=[O:8])[CH:7]=1참가 물질
9
반응물 5
생성물 1
시약·촉매·용매 3
반응 조건
- 온도
- 190 °C
실험 절차
A mixture of 4-hydroxy-6-oxo-1,6-dihydropyridine-3-carbonitrile (200 mg, 1.469 mmol, Medinoah), 1-bromo-4-(methylsulfonyl)benzene (345 mg, 1.469 mmol), 4,7-dimethoxy-1,10-phenanthroline (70.6 mg, 0.294 mmol), copper(I) iodide (56.0 mg, 0.294 mmol) and potassium carbonate (609 mg, 4.41 mmol) in DMSO (3 mL) was heated at 190° C. To the reaction mixture was added H2O (10 mL) and the pH adjusted to ˜2 using with 1N HCl. The resulting aqueous mixture was extracted with EtOAc (40 mL, 2×). The combined extracts were dried over Na2SO4 and concentrated to give a brown oil. The crude oil was purified by flash chromatography (SiO2, 0-5% MeOH/CH2Cl2) to give a yellow solid (35 mg, 0.084 mmol, 5.74%). MS (ESI) 291 (M+H).
후처리
- extractionThe resulting aqueous mixture was extracted with EtOAc (40 mL, 2×)
- dry with materialThe combined extracts were dried over Na2SO4
- concentrationconcentrated
- customto give a brown oil
- customThe crude oil was purified by flash chromatography (SiO2, 0-5% MeOH/CH2Cl2)
출처 및 근거
- ORD 기록
- ord-ccce094df6ae4c04a6a2ca0ae9716e4a
- 출처 데이터셋
- uspto-grants-2012_07
- 특허 번호
- US08232404B2
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