反応式
Cl[C:2]1[CH:11]=[N:10][C:9]2[C:4](=[CH:5][CH:6]=[C:7]([Cl:12])[CH:8]=2)[N:3]=1.[OH:13][C:14]1[CH:30]=[CH:29][C:17]([O:18][CH:19]([CH3:28])[C:20]([O:26][CH3:27])=[CH:21][C:22]([O:24][CH3:25])=[O:23])=[CH:16][CH:15]=1>>[Cl:12][C:7]1[CH:8]=[C:9]2[C:4](=[CH:5][CH:6]=1)[N:3]=[C:2]([O:13][C:14]1[CH:15]=[CH:16][C:17]([O:18][CH:19]([CH3:28])[C:20]([O:26][CH3:27])=[CH:21][C:22]([O:24][CH3:25])=[O:23])=[CH:29][CH:30]=1)[CH:11]=[N:10]2参加物
3
実験手順
The procedure of Example 37 is repeated using 2,6-dichloroquinoxaline and methyl 4-(4-hydroxyphenoxy)-3-methoxy-2-pentenoate as the starting materials to yield methyl 4-[4-(6-chloro-2-quinoxalyloxy)phenoxy]-3-methoxy-2-pentenoate which is treated with 35% HClO4 to yield the 3-oxo ester. Methyl 4-[4-(6-chloro-2-quinoxalyloxy)phenoxy]-3-oxopentanoate.
出典と根拠
- ORDレコード
- ord-c8b7876b8696489d98d06c70e2589ed5
- 出典データセット
- uspto-grants-1985_07
- 特許番号
- US04529438
関連ノート
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