Hydrochloric Acid → 1-(5-(Trifluoromethyl)pyridin-3-yl)piperazine
反応式
[F:1][C:2]([F:23])([F:22])[C:3]1[CH:4]=[C:5]([N:9]2[CH2:14][CH2:13][N:12](C(OC(C)(C)C)=O)[CH2:11][CH2:10]2)[CH:6]=[N:7][CH:8]=1.Cl>O1CCOCC1>[F:22][C:2]([F:1])([F:23])[C:3]1[CH:4]=[C:5]([N:9]2[CH2:14][CH2:13][NH:12][CH2:11][CH2:10]2)[CH:6]=[N:7][CH:8]=1参加物
4
実験手順
tert-Butyl 4-[5-(trifluoromethyl)pyridin-3-yl]piperazine-1-carboxylate (0.24 g, 0.25 mmol) was treated with a 4.0 M solution of HCl in 1,4-dioxane (7 mL) at room temperature for 1 h and concentrated. The residue was used for next step without further purification. MS calculated for C10H12F3N3: (M+H) 232; found 232.1.
後処理
- concentrationconcentrated
- customThe residue was used for next step without further purification
出典と根拠
- ORDレコード
- ord-fe5569ae421746fcbe5e213b450692ed
- 出典データセット
- uspto-grants-2013_10
- 特許番号
- US08563582B2
反応ノート
読み込み中…