反応式
[N:1]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[C:3]([C:11]([OH:13])=O)[C:2]=1[C:14]([OH:16])=[O:15].C(OC(=O)C)(=O)C>>[N:1]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[C:3]2[C:11]([O:16][C:14](=[O:15])[C:2]=12)=[O:13]参加物
3
実験手順
Following isolation, the formula (VIII) quinoline-2,3-dicarboxylic acid is heated to about 70° to 95° C. with an excess of acetic anhydride to yield the formula (IV) 2,3-quinolinedicarboxylic acid anhydride, having the structure: ##STR8## wherein L, M, Q and R7 are as described above. A cosolvent such as pyridine or pyridine-dimethoxyethane may also be used in this reaction, but is not essential to obtain the desired product.
出典と根拠
- ORDレコード
- ord-8bf21d2f67544349a95dd0e7bade5524
- 出典データセット
- uspto-grants-1987_04
- 特許番号
- US04656283
関連ノート
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