反応式
[F:1][CH:2]1[N:8](S(C2C=CC(C)=CC=2)(=O)=O)[CH:7]([C:19]2[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=2)[C:6]2[CH:25]=[C:26]([N+:29]([O-:31])=[O:30])[CH:27]=[CH:28][C:5]=2[NH:4][C:3]1=[O:32].C1(C)C=CC(S(N2C(C3C=CC=CC=3)C3C=C([N+]([O-])=O)C=CC=3NC(=O)C2)(=O)=O)=CC=1.C(OF)(F)(F)F>CN(C=O)C>[F:1][CH:2]1[N:8]=[C:7]([C:19]2[CH:20]=[CH:21][CH:22]=[CH:23][CH:24]=2)[C:6]2[CH:25]=[C:26]([N+:29]([O-:31])=[O:30])[CH:27]=[CH:28][C:5]=2[NH:4][C:3]1=[O:32]参加物
5
反応物 3
生成物 1
試薬・触媒・溶媒 1
実験手順
2.35 g. of sublimed potassium tert.-butylate are added at 5° to a solution of 4.55 g. of 3-fluoro-4-p-toluenesulfonyl-5-phenyl-7-nitro-2,3,4,5-tetrahydro-1H-1,4-benzodiazepin-2-one, obtainable from 4-p-toluenesulfonyl-5-phenyl-7-nitro-2,3,4,5-tetrahydro-1H-1,4-benzodiazepin-2-one and CF3OF, in 50 ml. of DMF. After stirring for 1 hour, the temperature is allowed to rise to 20° and the mixture is stirred for 48 hours more. The mixture is poured onto ice and worked up in the customary manner to give 3-fluoro-5-phenyl-7-nitro-2,3-dihydro-1H-1,4-benzodiazepin-2-one.
後処理
- customto rise to 20°
- stirringthe mixture is stirred for 48 hours more
- additionThe mixture is poured onto ice
出典と根拠
- ORDレコード
- ord-930db9717e944bd3a8b5d05a3ffb243a
- 出典データセット
- uspto-grants-1980_11
- 特許番号
- US04232016
関連ノート
読み込み中…