Diethyl (ethoxymethylene)malonate → 4-Chloro-6-methylquinoline
反応式
[Cl:1][C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[C:9](F)[CH:10]=2)[N:5]=[CH:4][CH:3]=1.N[C:14]1C=CC(C)=CC=1.C(OC=C(C(OCC)=O)C(OCC)=O)C>>[Cl:1][C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[C:9]([CH3:14])[CH:10]=2)[N:5]=[CH:4][CH:3]=1参加物
4
実験手順
This compound was made in a manner analogous to that of the synthesis of 4-chloro-6-fluoroquinoline described in Example 12. Starting from p-toluidine and diethyl ethoxymethylenemalonate the compound was obtained as a solid of mp 47°-51°.
後処理
- customwas obtained as a solid of mp 47°-51°
出典と根拠
- ORDレコード
- ord-22feae69b3004835bd9dbcaf9ec499ba
- 出典データセット
- uspto-grants-1985_12
- 特許番号
- US04560692
反応ノート
読み込み中…