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[N:1]1([N:7]2[NH:11][CH:10]=[C:9]([C:12]3[N:13]([CH3:20])[C:14]([N+:17]([O-:19])=[O:18])=[CH:15][N:16]=3)[S:8]2)[CH2:6][CH2:5]C[CH2:3][CH2:2]1.[NH:21]1CCNCC1.N1CCCCC1>>[N:1]1([N:7]2[NH:11][CH:10]=[C:9]([C:12]3[N:13]([CH3:20])[C:14]([N+:17]([O-:19])=[O:18])=[CH:15][N:16]=3)[S:8]2)[CH2:6][CH2:5][NH:21][CH2:3][CH2:2]1참가 물질
4
실험 절차
The preparation of the subject compound is carried out essentially as described for the 2-piperidino derivative (Example 28), two equivalents of piperazine replacing the piperidine. The crude project is recrystallized from 2-methoxyethanol to yield the pure compound melting at 240°-241° C. ;cl EXAMPLE 24
후처리
- customThe preparation of the subject compound
- customThe crude project is recrystallized from 2-methoxyethanol
출처 및 근거
- ORD 기록
- ord-12914646f91d4db4b530caf5515c91e9
- 출처 데이터셋
- uspto-grants-1977_12
- 특허 번호
- US04065567
연결된 노트
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