反応式
[Cl:1][C:2]1[CH:3]=[C:4]([C:17]([O:19]C)=[O:18])[C:5]2[O:9][C:8]([C:10]3[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=3)=[N:7][C:6]=2[CH:16]=1.[OH-].[Li+]>>[Cl:1][C:2]1[CH:3]=[C:4]([C:17]([OH:19])=[O:18])[C:5]2[O:9][C:8]([C:10]3[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=3)=[N:7][C:6]=2[CH:16]=1参加物
3
実験手順
5-Chloro-2-phenylbenzoxazole-7-carboxylic acid was prepared from methyl 5-chloro-2-phenyl-benzoxazole-7-carboxylate via lithium hydroxide mediated hydrolysis as described in Step B of Example 14. This material was obtained as a white solid in 82% yield. 1H NMR (300 MHz, DMSO-d6) δ 13.84 (br s, 1H), 8.22-8.19 (m, 3H), 7.85 (d, J=2.1 Hz, 1H), 7.70-7.63 (m, 3H), 4.07 (s, 3H); MS (ESI) m/z 274 [M+H]+.
後処理
- customhydrolysis
- customThis material was obtained as a white solid in 82% yield
出典と根拠
- ORDレコード
- ord-945d2baad0494423afb1666aca8cfc33
- 出典データセット
- uspto-grants-2010_08
- 特許番号
- US07781430B2
関連ノート
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