HCID 58446972、化合物 → HCID 58446997、化合物
反応式
[Br:1][C:2]1[C:3]([N:21]=[CH:22][NH:23]O)=[N:4][C:5]([N:8]2[CH2:13][CH2:12][N:11](C(OC(C)(C)C)=O)[CH2:10][CH2:9]2)=[N:6][CH:7]=1>[OH-].[K+]>[Br:1][C:2]1[C:3]2[N:4]([N:23]=[CH:22][N:21]=2)[C:5]([N:8]2[CH2:13][CH2:12][NH:11][CH2:10][CH2:9]2)=[N:6][CH:7]=1参加物
3
反応条件
- 温度
- 100 °C
実験手順
A 100 mL round bottom flask was charged with tert-butyl 4-(5-bromo-4-(((hydroxyamino)methylene)amino)pyrimidin-2-yl)piperazine-1-carboxylate (1.1 g) and polyphosphoric acid (20 g). The resulting mixture was stirred at 100° C. overnight. Work-up: the reaction mixture was carefully diluted with saturated aqueous KOH (300 mL) and then extracted with CH2Cl2 (100 mL×3). The combined organic layers were dried over anhydrous Na2SO4 and concentrated in vacuo. The residue was purified by flash column chromatography on silica gel to afford 0.3 g (39%) of the product as a white solid. MS m/z: 283 (M+H+).
後処理
- extractionextracted with CH2Cl2 (100 mL×3)
- dry with materialThe combined organic layers were dried over anhydrous Na2SO4
- concentrationconcentrated in vacuo
- customThe residue was purified by flash column chromatography on silica gel
出典と根拠
- ORDレコード
- ord-65e29874661e4830b05b7ac650b65b14
- 出典データセット
- uspto-grants-2013_10
- 特許番号
- US08569300B2
反応ノート
読み込み中…