N,N-dimethyl-N-(4-nitrophenyl)carbamylmethyl-N-3-formamidopropylammonium chloride → N,N-dimethyl-N-(4-aminophenyl)carbamylmethyl-N-3-formamidopropylammonium chloride

HRID 614721

反応式

[Cl-:1].[CH3:2][N+:3]([CH3:23])([CH2:10][C:11](=[O:22])[NH:12][C:13]1[CH:18]=[CH:17][C:16]([N+:19]([O-])=O)=[CH:15][CH:14]=1)[CH2:4][CH2:5][CH2:6][NH:7][CH:8]=[O:9]>[Pt]=S>[Cl-:1].[CH3:23][N+:3]([CH3:2])([CH2:10][C:11](=[O:22])[NH:12][C:13]1[CH:18]=[CH:17][C:16]([NH2:19])=[CH:15][CH:14]=1)[CH2:4][CH2:5][CH2:6][NH:7][CH:8]=[O:9]

参加物

実験手順

Following the procedure described in 1c above, N,N-dimethyl-N-(4-nitrophenyl)carbamylmethyl-N-3-formamidopropylammonium chloride was catalytically hydrogenated in aqueous solution at 70°-75° C. and at 600 pounds per square inch in the presence of a 5 percent platinum sulfide on charcoal mixture to obtain N,N-dimethyl-N-(4-aminophenyl)carbamylmethyl-N-3-formamidopropylammonium chloride.

出典と根拠

ORDレコード: ord-d289353742de491aa950d1975dc0b7ec
出典データセット: uspto-grants-1979_03
DOI: 10.6084/m9.figshare.5104873.v1
特許番号: US04146558

反応式

参加物

反応物 1

生成物 1

試薬・触媒・溶媒 1

実験手順

出典と根拠

関連ノート