반응식
[OH:1][C:2]1[CH2:7][CH:6]([C:8]2[C:13]([CH3:14])=[CH:12][C:11]([CH3:15])=[CH:10][C:9]=2[CH3:16])[CH2:5][C:4](=[O:17])[C:3]=1[C:18](=O)[CH2:19][CH3:20].Cl[S:23]([OH:26])(=O)=[O:24].[CH3:27][NH:28][CH3:29].Cl.[CH2:31]([O:33][NH2:34])[CH3:32]>>[CH2:31]([O:33][N:34]=[C:18]([C:3]1[C:4](=[O:17])[CH2:5][CH:6]([C:8]2[C:13]([CH3:14])=[CH:12][C:11]([CH3:15])=[C:10]([S:23](=[O:26])(=[O:24])[N:28]([CH3:29])[CH3:27])[C:9]=2[CH3:16])[CH2:7][C:2]=1[OH:1])[CH2:19][CH3:20])[CH3:32]참가 물질
5
실험 절차
2-[1-(Ethoxyimino)propyl]-3-hydroxy-5-(2,4,6-trimethyl-3-dimethylsulfamoylphenyl)cyclohex-2-en-1-one (11) was prepared from 3-hydroxy-5-mesityl-2-propionylcyclohex-2-en-1-one, chlorosulfonic acid, dimethylamine, and ethoxyamine hydrochloride following essentially the same procedure as that described in Example 5.
출처 및 근거
- ORD 기록
- ord-8996f2393cca440f9c39eb2b1fc5caad
- 출처 데이터셋
- uspto-grants-1987_05
- 특허 번호
- US04666510
연결된 노트
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