反応式
[Br:1][C:2]1[C:3]([CH3:9])=[C:4]([CH:6]=[CH:7][CH:8]=1)[NH2:5].C(N(C(C)C)CC)(C)C.ClCCl.[C:22]12([C:32](Cl)=[O:33])[CH2:31][CH:26]3[CH2:27][CH:28]([CH2:30][CH:24]([CH2:25]3)[CH2:23]1)[CH2:29]2>C(OCC)(=O)C>[Br:1][C:2]1[C:3]([CH3:9])=[C:4]([NH:5][C:32]([C:22]23[CH2:31][CH:26]4[CH2:25][CH:24]([CH2:30][CH:28]([CH2:27]4)[CH2:29]2)[CH2:23]3)=[O:33])[CH:6]=[CH:7][CH:8]=1参加物
6
実験手順
3-Bromo-2-methylaniline (800 mg) and diisopropylethylamine (1667 mg) were added to dichloromethane (12 mL). 1-Adamantanecarbonyl chloride (940 mg) was added and the solution was stirred at room temperature for 16 hours. The solution was diluted with 50% ethyl acetate (hexanes), washed three times with 1 M aqueous HCl, washed with brine, dried over anhydrous sodium sulfate, and filtered. The solvent volume was partially reduced under vacuum, and the solid material precipitated out of solution, which was isolated by filtration to provide the title compound.
後処理
- washwashed three times with 1 M aqueous HCl
- washwashed with brine
- dry with materialdried over anhydrous sodium sulfate
- filtrationfiltered
- customthe solid material precipitated out of solution
- customwhich was isolated by filtration
出典と根拠
- ORDレコード
- ord-7c8f4e9fc1fb4d9b8c9f8978a82eb989
- 出典データセット
- uspto-grants-2014_11
- 特許番号
- US08889675B2
関連ノート
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