{2-(4-Hydroxy-phenyl)-1-[1-methylcarbamoyl-2-(4-nitro-phenyl)-ethylcarbamoyl]-ethyl} carbamic acid tert-butyl ester → {2-(4-Hydroxy-phenyl)-1-[1-methylcarbamoyl-2-(4-amino-phenyl)-ethylcarbamoyl]-ethyl}-carbamic acid tert-butyl ester

HRID 500102

反応式

HRID 500102 の反応式
[C:1]([O:5][C:6](=[O:35])[NH:7][CH:8]([C:17](=[O:34])[NH:18][CH:19]([C:30](=[O:33])[NH:31][CH3:32])[CH2:20][C:21]1[CH:26]=[CH:25][C:24]([N+:27]([O-])=O)=[CH:23][CH:22]=1)[CH2:9][C:10]1[CH:15]=[CH:14][C:13]([OH:16])=[CH:12][CH:11]=1)([CH3:4])([CH3:3])[CH3:2]>CO.[Pd]>[C:1]([O:5][C:6](=[O:35])[NH:7][CH:8]([C:17](=[O:34])[NH:18][CH:19]([C:30](=[O:33])[NH:31][CH3:32])[CH2:20][C:21]1[CH:26]=[CH:25][C:24]([NH2:27])=[CH:23][CH:22]=1)[CH2:9][C:10]1[CH:11]=[CH:12][C:13]([OH:16])=[CH:14][CH:15]=1)([CH3:4])([CH3:2])[CH3:3]

参加物

4

実験手順

{2-(4-Hydroxy-phenyl)-1-[1-methylcarbamoyl-2-(4-nitro-phenyl)-ethylcarbamoyl]-ethyl}carbamic acid tert-butyl ester (300, 0.617 mmol) is dissolved in methanol (10 mL). To this was added palladium on carbon (10% by weight, 100 mg). The reaction is placed under a hydrogen atmosphere until reaction is complete (tlc). The catalyst is removed by filtration and the filtrate is concentrated to provide the amine, which is used without purification.

後処理

  1. customThe reaction is placed under a hydrogen atmosphere until reaction
  2. customThe catalyst is removed by filtration
  3. concentrationthe filtrate is concentrated

出典と根拠

ORDレコード
ord-0d09edfc7d5a45708ad6f556debc364c
出典データセット
uspto-grants-2010_08
特許番号
US07769575B2

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