Pyridine → 2-(7-fluoro-4-propargyl-2H-1,4-benzoxazin-3(4H)-on-6-yl)-4,5,6,7-tetrahydro-1,2,3-benzotriazole-1-oxide
反応式
[F:1][C:2]1[C:15]([NH:16][NH:17][CH:18]2[CH2:23][CH2:22][CH2:21][CH2:20][C:19]2=[N:24][OH:25])=[CH:14][C:5]2[N:6]([CH2:11][C:12]#[CH:13])[C:7](=[O:10])[CH2:8][O:9][C:4]=2[CH:3]=1.N1C=CC=CC=1>O1CCCC1.O.S([O-])([O-])(=O)=O.[Cu+2]>[F:1][C:2]1[C:15]([N:16]2[N+:24]([O-:25])=[C:19]3[CH2:20][CH2:21][CH2:22][CH2:23][C:18]3=[N:17]2)=[CH:14][C:5]2[N:6]([CH2:11][C:12]#[CH:13])[C:7](=[O:10])[CH2:8][O:9][C:4]=2[CH:3]=1参加物
6
反応物 2
生成物 1
試薬・触媒・溶媒 3
反応条件
- 温度
- 80 °C
実験手順
To a solution of 2-[2-(7-fluoro-4-propargyl-2H-1,4-benzoxazin-3(4H)-on-6-yl)hydrazino]cyclohexanone oxime (0.4 g) in tetrahydrofuran (6 ml), 15% aqueous pyridine (7 g) was added, and a solution of copper sulfate (0.7 g) in water (1.5 ml) was added thereto, followed by heating at 80° C. for 2 hours. The reaction mixture was allowed to cool, combined with water and extracted with ethyl acetate. The organic layer was washed with 10% aqueous copper sulfate solution, dried and concentrated. The residue was purified by silica gel column chromatography using ethyl acetate as an eluent to give Compound No. 1 (0.2 g). m.p., 186°-187° C.
後処理
- temperatureto cool
- extractionextracted with ethyl acetate
- washThe organic layer was washed with 10% aqueous copper sulfate solution
- customdried
- concentrationconcentrated
- customThe residue was purified by silica gel column chromatography
- customto give Compound No
- customm.p., 186°-187° C.
出典と根拠
- ORDレコード
- ord-542bd86611a448529b031e8b1afeaf4c
- 出典データセット
- uspto-grants-1989_12
- 特許番号
- US04885024
反応ノート
読み込み中…