HCID 6465104、化合物 → HCID 68680371、化合物
反応式
C[O:2][C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][C:4]=1[CH2:9][CH2:10][NH:11][S:12]([C:15]1[CH:20]=[CH:19][C:18]([CH3:21])=[CH:17][CH:16]=1)(=[O:14])=[O:13].FC1C=CC(OC2C=CC(S(NCCC3C=CC=CC=3O)(=O)=O)=CC=2)=CC=1>>[OH:2][C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][C:4]=1[CH2:9][CH2:10][NH:11][S:12]([C:15]1[CH:16]=[CH:17][C:18]([CH3:21])=[CH:19][CH:20]=1)(=[O:14])=[O:13]参加物
3
実験手順
The title compound is prepared starting from N-[2-(2-methoxyphenyl)ethyl]-4-methylbenzenesulfonamide in analogy to the method described under 19B, it likewise being possible for the crude product to be reacted further without further purification.
後処理
- customto be reacted further without further purification
出典と根拠
- ORDレコード
- ord-6def471736164d988dd9ede3fd8e3eb6
- 出典データセット
- uspto-grants-2010_12
- 特許番号
- US07858619B2
反応ノート
読み込み中…