反応式
[Cl:1][C:2]1[C:7]([OH:8])=[CH:6][C:5]([NH:9][C:10](=O)[C:11]2[CH:16]=[CH:15][C:14]([OH:17])=[C:13]([F:18])[CH:12]=2)=[C:4]([OH:20])[CH:3]=1.Cl.N1C=CC=CC=1>>[Cl:1][C:2]1[C:7]([OH:8])=[CH:6][C:5]2[N:9]=[C:10]([C:11]3[CH:16]=[CH:15][C:14]([OH:17])=[C:13]([F:18])[CH:12]=3)[O:20][C:4]=2[CH:3]=1参加物
3
実験手順
The title compound was prepared in substantially the same manner as described in Example 1, step b, from N-(4-chloro-2,5-dihydroxyphenyl)-3-fluoro-4-hydroxybenzamide and pyridine hydrochloride and was obtained as a white solid, m.p. 258–260° C.; MS m/e 278 (M−H)+.
後処理
- customwas obtained as a white solid, m.p. 258–260° C.
出典と根拠
- ORDレコード
- ord-ca6ad7f61aa549fda28e56862a595561
- 出典データセット
- uspto-grants-2006_10
- 特許番号
- US07129258B2
関連ノート
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