4-Isopropylaniline → N-(4-isopropylphenyl)-3-(phenylsulfonyl)benzamide
反応式
[C:1]1([S:7]([C:10]2[CH:11]=[C:12]([CH:16]=[CH:17][CH:18]=2)[C:13]([OH:15])=O)(=[O:9])=[O:8])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[CH:19]([C:22]1[CH:28]=[CH:27][C:25]([NH2:26])=[CH:24][CH:23]=1)([CH3:21])[CH3:20]>>[CH:19]([C:22]1[CH:28]=[CH:27][C:25]([NH:26][C:13](=[O:15])[C:12]2[CH:16]=[CH:17][CH:18]=[C:10]([S:7]([C:1]3[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=3)(=[O:8])=[O:9])[CH:11]=2)=[CH:24][CH:23]=1)([CH3:21])[CH3:20]参加物
3
実験手順
The entitled compound was produced according to the method of Example 92 but using 3-(phenylsulfonyl)benzoic acid and 4-isopropylaniline as the starting materials.
後処理
- customThe entitled compound was produced
出典と根拠
- ORDレコード
- ord-c0466ecbc6334eae8c19a41be7432444
- 出典データセット
- uspto-grants-2013_04
- 特許番号