反応式
[Cl:1][C:2]1[CH:10]=[CH:9][C:5]([C:6]([NH2:8])=[O:7])=[CH:4][CH:3]=1.[F:11][C:12]([F:19])([F:18])[C:13]([F:17])([F:16])[CH:14]=O.[NH:20]1[C:24]2[CH:25]=[CH:26][CH:27]=[CH:28][C:23]=2[N:22]=[N:21]1.C1(C)C=CC(S(O)(=O)=O)=CC=1>>[N:20]1([CH:14]([NH:8][C:6](=[O:7])[C:5]2[CH:9]=[CH:10][C:2]([Cl:1])=[CH:3][CH:4]=2)[C:13]([F:17])([F:16])[C:12]([F:19])([F:18])[F:11])[C:24]2[CH:25]=[CH:26][CH:27]=[CH:28][C:23]=2[N:22]=[N:21]1参加物
5
実験手順
4-Chlorobenzamide, pentafluoropropanal, benzotriazole, and p-toluenesulfonic acid were processed as described in Example 53A to provide the desired product.
出典と根拠
- ORDレコード
- ord-eb2449b977e846489132bb5e60b96796
- 出典データセット
- uspto-grants-2003_11
- 特許番号
- US06645968B2
関連ノート
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