1-Piperazinecarbothioamide → 1-[4-(2,2,2-Trifluoro-ethyl)-thiazol-2-yl]-piperazine
反応式
[N:1]1([C:7](=[S:9])[NH2:8])[CH2:6][CH2:5][NH:4][CH2:3][CH2:2]1.Br[CH2:11][C:12](=O)[CH2:13][C:14]([F:17])([F:16])[F:15]>>[F:15][C:14]([F:17])([F:16])[CH2:13][C:12]1[N:8]=[C:7]([N:1]2[CH2:6][CH2:5][NH:4][CH2:3][CH2:2]2)[S:9][CH:11]=1参加物
3
実験手順
Prepared in analogy to example 49 (a) from 1-piperazinecarbothioamide and 1-bromo-4,4,4-trifluoro-butan-2-one. The crude material was purified by chromatography (SiO2, methanol/dichloromethane) to yield the title compound as a brown oil (yield 24%). MS (m/e): 252.3 (M+H+, 100%).
後処理
- customThe crude material was purified by chromatography (SiO2, methanol/dichloromethane)
出典と根拠
- ORDレコード
- ord-eedcf6cd32484b7e84ee966bda90eaca
- 出典データセット
- uspto-grants-2007_05
- 特許番号
- US07220744B2
反応ノート
読み込み中…