N-(2-methoxy-5-nitrophenyl)methanesulfonamide → N-(5-amino-2-methoxyphenyl)methanesulfonamide

HRID 19975

反応式

HRID 19975 の反応式
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([N+:9]([O-])=O)=[CH:5][C:4]=1[NH:12][S:13]([CH3:16])(=[O:15])=[O:14]>CO.[Pd]>[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([NH2:9])=[CH:5][C:4]=1[NH:12][S:13]([CH3:16])(=[O:15])=[O:14]

参加物

4

反応物 1

HCID 743556N-(2-methoxy-5-nitrophenyl)methanesulfonamide

生成物 1

HCID 10775094N-(5-amino-2-methoxyphenyl)methanesulfonamide

試薬・触媒・溶媒 2

HCID 23938Palladium触媒HCID 887Methanol溶媒

実験手順

A solution of 2-Methoxy-5-nitro-methanesulfonylaminobenzene (1 g) in methanol (20 ml) containing palladium on carbon (10%, 100 mg) was stirred at RT under hydrogen for 48 h. The mixture was filtered through celite then evaporated to give 2-methoxy-5-amino-methanesulfonylaminobenzene as a brown gum. This was used without purification in the following reaction.

後処理

  1. filtrationThe mixture was filtered through celite
  2. customthen evaporated

出典と根拠

ORDレコード
ord-8b2221c0082a4c95abf5c3c40f2e6318
出典データセット
uspto-grants-2010_06
特許番号
US07745490B2

関連ノート

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