반응식
[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]=1참가 물질
4
실험 절차
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°.
후처리
- customwas obtained as a solid of mp 47°-51°
출처 및 근거
- ORD 기록
- ord-22feae69b3004835bd9dbcaf9ec499ba
- 출처 데이터셋
- uspto-grants-1985_12
- 특허 번호
- US04560692
연결된 노트
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