4-(4-Benzylaminosulfonylmethylbenzyl)-nitrobenzene → 4-(4-Benzylaminosulfonylmethylbenzyl)-phenylamine
反応式
[CH2:1]([NH:8][S:9]([CH2:12][C:13]1[CH:28]=[CH:27][C:16]([CH2:17][C:18]2[CH:23]=[CH:22][C:21]([N+:24]([O-])=O)=[CH:20][CH:19]=2)=[CH:15][CH:14]=1)(=[O:11])=[O:10])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1>C(OCC)(=O)C.[Pd]>[CH2:1]([NH:8][S:9]([CH2:12][C:13]1[CH:14]=[CH:15][C:16]([CH2:17][C:18]2[CH:19]=[CH:20][C:21]([NH2:24])=[CH:22][CH:23]=2)=[CH:27][CH:28]=1)(=[O:11])=[O:10])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1参加物
4
実験手順
A solution of 4-(4-benzylaminosulfonylmethylbenzyl)-nitrobenzene (44 mg) was dissolved in ethyl acetate and hydrogenated at 40 psi with 10% palladium on carbon catalyst for 2 hours. The mixture was filtered, and the solvent was evaported to give 4-(4-benzylaminosulfonylmethylbenzyl)-phenylamine (39 mg) as an off-white solid.
後処理
- filtrationThe mixture was filtered
出典と根拠
- ORDレコード
- ord-10a620ee54fe432099073948578b0a51
- 出典データセット
- uspto-grants-2001_02
- 特許番号
- US06184242B2
反応ノート
読み込み中…