Hexane → 5-Bromo-4-tert-butyl-1,3-thiazol-2-amine
反応式
[NH2:1][C:2]1[S:3][CH:4]=[C:5]([C:7]([CH3:10])([CH3:9])[CH3:8])[N:6]=1.[Br:11]N1C(=O)CCC1=O.CCCCCC>C(Cl)(Cl)(Cl)Cl>[NH2:1][C:2]1[S:3][C:4]([Br:11])=[C:5]([C:7]([CH3:10])([CH3:9])[CH3:8])[N:6]=1参加物
5
実験手順
2-Amino-4-[(1,1-dimethyl)ethyl]thiazole (compound of Example 181(1); 0.87 g, 5.6 mmol) was dissolved in carbon tetrachloride (9 mL). N-Bromosuccinimide (1.00 g, 5.6 mmol) was added, and the mixture was stirred at room temperature for 1 hour. Hexane was added to the reaction mixture. The insoluble matter was filtered off, and the residue obtained by evaporation of the filtrate under reduced pressure was purified by chromatography on silica gel (hexane:ethyl acetate=2:1) to give the title compound (1.23 g, 93.7%) as an yellowish gray powder.
後処理
- filtrationThe insoluble matter was filtered off
- customthe residue obtained by evaporation of the filtrate under reduced pressure
- customwas purified by chromatography on silica gel (hexane:ethyl acetate=2:1)
出典と根拠
- ORDレコード
- ord-7a79036d05b44beabd86e65881402ec7
- 出典データセット
- uspto-grants-2010_04
- 特許番号
- US07700655B2
反応ノート
読み込み中…