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
反応式
[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]=1参加物
反応物 4
生成物 1
試薬・触媒・溶媒 1
実験手順
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).
後処理
- 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)
出典と根拠
- ORDレコード
- ord-9c64077b249a43d285b3321f6cae5c78
- 出典データセット
- uspto-grants-2013_01
- 特許番号
- US08354442B2
反応ノート
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