반응식
[NH2:1][C:2]1[C:7]([Cl:8])=[C:6]([CH3:9])[C:5]([Cl:10])=[C:4]([CH3:11])[N:3]=1.[OH-].[K+].[N+:14]([C:17]1[CH:22]=[C:21]([N+:23]([O-:25])=[O:24])[CH:20]=[C:19]([C:26]([F:29])([F:28])[F:27])[C:18]=1Cl)([O-:16])=[O:15]>CN(C)C=O>[Cl:8][C:7]1[C:2]([NH:1][C:18]2[C:19]([C:26]([F:28])([F:29])[F:27])=[CH:20][C:21]([N+:23]([O-:25])=[O:24])=[CH:22][C:17]=2[N+:14]([O-:16])=[O:15])=[N:3][C:4]([CH3:11])=[C:5]([Cl:10])[C:6]=1[CH3:9]참가 물질
5
실험 절차
In 20 ml. of dimethylformamide, 1.9 g. of 2-amino-3,5-dichloro-4,6-dimethylpyridine was dissolved and 0.7 g. of powdery potassium hydroxide was gradually added with stirring and a solution of 2.7 g. of 2,4-dinitro-6-trifluoromethylchlorobenzene in 10 ml. of dimethylformamide was added dropwise at room temperature to react them for about 10 hours. The reaction mixture was treated as the process of Preparation No. 7 to obtain 1.6 g. of the object compound having the melting point of 131° to 133° C.
후처리
- customto react them for about 10 hours
- additionThe reaction mixture was treated as the process of Preparation No
- custom7 to obtain 1.6 g
출처 및 근거
- ORD 기록
- ord-1c7e097d51ff48ea8a22f98e6342a625
- 출처 데이터셋
- uspto-grants-1982_05
- 특허 번호
- US04331670
연결된 노트
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