Water → 2-[5-(4-Chloro-phenyl)-1-(2,4-dichloro-phenyl)-4-methyl-1H-pyrazol-3-yl]-3,5,5-trimethyl-3,5-dihydro-imidazol-4-one
반응식
[H-].[Na+].[Cl:3][C:4]1[CH:9]=[CH:8][C:7]([C:10]2[N:14]([C:15]3[CH:20]=[CH:19][C:18]([Cl:21])=[CH:17][C:16]=3[Cl:22])[N:13]=[C:12]([C:23]3[NH:27][C:26](=[O:28])[C:25]([CH3:30])([CH3:29])[N:24]=3)[C:11]=2[CH3:31])=[CH:6][CH:5]=1.[CH3:32]I.O>CN(C=O)C>[Cl:3][C:4]1[CH:9]=[CH:8][C:7]([C:10]2[N:14]([C:15]3[CH:20]=[CH:19][C:18]([Cl:21])=[CH:17][C:16]=3[Cl:22])[N:13]=[C:12]([C:23]3[N:27]([CH3:32])[C:26](=[O:28])[C:25]([CH3:29])([CH3:30])[N:24]=3)[C:11]=2[CH3:31])=[CH:6][CH:5]=1참가 물질
반응물 4
생성물 1
시약·촉매·용매 1
실험 절차
To a solution of sodium hydride (14.4 mg, 0.66 mole) in DMF (3 mL) at 0° C. was added compound 23 (100 mg, 0.22 mmol) in one portion. The mixture was allowed to warm to room temperature and stirred for 30 min, at which time methyl iodide (2 g, 14.08 mmol) was added. After the mixture was stirred for 2 h, water was added and the resulting mixture was extracted with ethyl acetate (2×50 mL). The combined extracts were washed with brine, dried over anhydrous sodium sulfate, filtered, and concentrated. Purification of the crude residue by flash chromatography on silica gel with hexanes/ethyl acetate (1:1) gave the product 27 (70 mg, 0.15 mmol, 68%) as a white solid. 1H NMR (400 MHz, CDCl3) δ 7.45 (d, 1H), 7.30 (d, 2H), 7.26 (dd, 1H), 7.18 (d, 1H), 7.07 (d, 2H), 3.28 (s, 3H), 2.24 (s, 3H), 1.87 (s, 6H); ESMS m/: 461.1 (M+1).
후처리
- additionwas added
- extractionthe resulting mixture was extracted with ethyl acetate (2×50 mL)
- washThe combined extracts were washed with brine
- dry with materialdried over anhydrous sodium sulfate
- filtrationfiltered
- concentrationconcentrated
- customPurification of the crude residue by flash chromatography on silica gel with hexanes/ethyl acetate (1:1)
출처 및 근거
- ORD 기록
- ord-9c64077b249a43d285b3321f6cae5c78
- 출처 데이터셋
- uspto-grants-2013_01
- 특허 번호
- US08354442B2
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