반응식
[Cl:1][CH2:2][C:3]([C:5]1[CH:10]=[CH:9][C:8]([CH:11]([CH3:13])[CH3:12])=[C:7]([S:14](=[O:17])(=[O:16])[NH2:15])[CH:6]=1)=[O:4].[CH2:18]([NH:20][C:21]([NH:23][CH2:24][CH3:25])=[S:22])[CH3:19]>>[ClH:1].[CH2:24]([N:23]1[C:3]([C:5]2[CH:10]=[CH:9][C:8]([CH:11]([CH3:13])[CH3:12])=[C:7]([S:14](=[O:17])(=[O:16])[NH2:15])[CH:6]=2)([OH:4])[CH2:2][S:22][C:21]1=[N:20][CH2:18][CH3:19])[CH3:25]참가 물질
3
실험 절차
5.5 g of 2-chloro-4'isopropyl-3'-sulfamoylacetophenone and 2.2 g of 1,3-diethylthio urea were reacted and worked up as prescribed in Example 12. Colorless solid body, decomposition beginning at 96° C, γC=N 1610 cm-1.
후처리
- customat 96° C
출처 및 근거
- ORD 기록
- ord-6d66f298bf38433788dccb257f970ab9
- 출처 데이터셋
- uspto-grants-1977_12
- 특허 번호
- US04061761
연결된 노트
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