3-(Chloromethyl)-5-(4-chlorophenyl)-1,2-oxazole → {4-[5-(4-Chloro-phenyl)-isoxazol-3-ylmethylsulfanyl]-5-methoxy-2-methyl-phenoxy}-acetic Acid
反応式
C[O:2][C:3](=[O:16])[CH2:4][O:5][C:6]1[CH:11]=[C:10]([O:12][CH3:13])[C:9]([SH:14])=[CH:8][C:7]=1[CH3:15].Cl[CH2:18][C:19]1[CH:23]=[C:22]([C:24]2[CH:29]=[CH:28][C:27]([Cl:30])=[CH:26][CH:25]=2)[O:21][N:20]=1>>[Cl:30][C:27]1[CH:26]=[CH:25][C:24]([C:22]2[O:21][N:20]=[C:19]([CH2:18][S:14][C:9]3[C:10]([O:12][CH3:13])=[CH:11][C:6]([O:5][CH2:4][C:3]([OH:2])=[O:16])=[C:7]([CH3:15])[CH:8]=3)[CH:23]=2)=[CH:29][CH:28]=1参加物
3
実験手順
The title compound was prepared in the manner analogous to Example 1F using 1D and 3-chloromethyl-5-(4-chloro-phenyl)-isoxazole. MS m/z 434 (M+1).
出典と根拠
- ORDレコード
- ord-1260d13ff383468c9697516626d210ec
- 出典データセット
- uspto-grants-2005_11