反応式
F[C:2]1C=CC=C2C=1C(=O)N(C1C=CC=CC=1)C([C@@H](NC1N=CN=C3C=1N=CN3)CC)=N2.[N+:32]([C:35]1[CH:43]=[CH:42][C:41](C)=[CH:40][C:36]=1[C:37]([OH:39])=O)([O-:34])=[O:33].FC1C=CC=C([N+]([O-])=O)C=1C(O)=O.[F:58][C:59]1[CH:65]=[CH:64][CH:63]=[C:62]([F:66])[C:60]=1[NH2:61].NC1C=CC=CC=1>>[F:58][C:59]1[CH:65]=[CH:64][CH:63]=[C:62]([F:66])[C:60]=1[NH:61][C:37](=[O:39])[C:36]1[C:35]([N+:32]([O-:34])=[O:33])=[CH:43][CH:42]=[CH:41][C:40]=1[CH3:2]参加物
6
実験手順
Compound 118a was prepared following the preparation procedure described above with respect to compound 107, but 2-nitro-5-methylbenzoic acid was substituted for 2-fluoro-6-nitrobenzoic acid and 2,6-difluoroaniline was substituted for aniline.
後処理
- customthe preparation procedure
出典と根拠
- ORDレコード
- ord-d59e7ee8af924843bc6ac5f7c6917486
- 出典データセット
- uspto-grants-2012_06
- 特許番号
- US08207153B2
関連ノート
読み込み中…