반응식
[CH:1]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][C:2]=1[C:11]([NH2:13])=[NH:12].[N+:14]([C:17]1[CH:28]=[CH:27][C:20]([CH:21]=[CH:22][S:23](Cl)(=[O:25])=[O:24])=[CH:19][CH:18]=1)([O-:16])=[O:15]>>[N+:14]([C:17]1[CH:18]=[CH:19][C:20]([CH:21]=[CH:22][S:23]([NH:12][C:11]([C:2]2[CH:3]=[CH:4][C:5]3[C:10](=[CH:9][CH:8]=[CH:7][CH:6]=3)[CH:1]=2)=[NH:13])(=[O:25])=[O:24])=[CH:27][CH:28]=1)([O-:16])=[O:15]참가 물질
3
실험 절차
Reaction of β-naphthamidine with 4-nitrostyrylsulfonyl chloride according to the above procedure affords N-(4-NITROSTYRYLSULFONYL)-β-NAPHTHAMIDINE, m.p. 180°-182.5° C., by triturating with isopropanol.
출처 및 근거
- ORD 기록
- ord-e486ecde99534aaa93869a06f06fe5d3
- 출처 데이터셋
- uspto-grants-1981_03
- 특허 번호
- US04259482
연결된 노트
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