反応式
[CH3:1][C:2]1[N:3]([C:8]2[CH:12]=[C:11]([CH:13]([CH3:15])[CH3:14])[NH:10][N:9]=2)[C:4]([CH3:7])=[CH:5][CH:6]=1.[H-].[Na+].N[C@H:19](C(O)=O)CCSC.[Cl-].[NH4+]>C1COCC1.C(Cl)Cl>[CH3:1][C:2]1[N:3]([C:8]2[N:9]([CH3:19])[N:10]=[C:11]([CH:13]([CH3:15])[CH3:14])[CH:12]=2)[C:4]([CH3:7])=[CH:5][CH:6]=1.[CH3:1][C:2]1[N:3]([C:8]2[CH:12]=[C:11]([CH:13]([CH3:15])[CH3:14])[N:10]([CH3:19])[N:9]=2)[C:4]([CH3:7])=[CH:5][CH:6]=1参加物
反応物 4
生成物 2
試薬・触媒・溶媒 2
実験手順
To a solution of 3-(2,5-dimethyl-pyrrol-1-yl)-5-isopropyl-1H-pyrazole (7.7 g, 37.9 mmol) in THF (400 mL) that is purged with nitrogen is added NaH (2.272 g, 56.8 mmol) at 0° C. The mixture is stirred for 10 min in the ice bath then for 10 min at room temperature. Met (4.74 mL, 76 mmol) is added and the mixture is stirred at room temperature for 1 h. At that point the reaction is diluted with DCM and treated with saturated solution of ammonium chloride (10 mL). The mixture is concentrated to dryness and the residue is partitioned in water and DCM. The organic layer is combined, dried over sodium sulfate, concentrated and absorbed onto silica to purify by FCC (0-30% EtOAC/Heptane) to give 5-(2,5-Dimethyl-pyrrol-1-yl)-3-isopropyl-1-methyl-1H-pyrazole (2.4 g, 29%) as the first peak and 3-(2,5-Dimethyl-pyrrol-1-yl)-5-isopropyl-1-methyl-1H-pyrazole (5.24 g, 63%) as the second peak. MS (ESI) m/z 218.3 (m+1).
後処理
- concentrationThe mixture is concentrated to dryness
- customthe residue is partitioned in water
- dry with materialdried over sodium sulfate
- concentrationconcentrated
- customabsorbed onto silica
- customto purify by FCC (0-30% EtOAC/Heptane)
出典と根拠
- ORDレコード
- ord-d0b6d568edcc42c4baf54071ba01d9ce
- 出典データセット
- uspto-grants-2013_09
- 特許番号
- US08541432B2
関連ノート
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