Methylamine → 2-Chloro-4-fluoro-5-[(methylamino)sulfonyl]benzoic acid

HRID 1992145

反応式

HRID 1992145 の反応式
[Cl:1][C:2]1[CH:10]=[C:9]([F:11])[C:8]([S:12](Cl)(=[O:14])=[O:13])=[CH:7][C:3]=1[C:4]([OH:6])=[O:5].[CH3:16][NH2:17]>>[Cl:1][C:2]1[CH:10]=[C:9]([F:11])[C:8]([S:12]([NH:17][CH3:16])(=[O:14])=[O:13])=[CH:7][C:3]=1[C:4]([OH:6])=[O:5]

参加物

3

実験手順

At 0° C., to a stirred ice-water suspension (˜200 mL) of 2-chloro-5-(chlorosulfonyl)-4-fluorobenzoic acid was slowly added a precooled 40% methylamine (13 mL). The reaction mixture was then stirred for 2 hours before being acidified to pH˜2. The desired product was precipitated and filtered out. After being dried overnight, the pure 2-chloro-4-fluoro-5-[(methylamino)sulfonyl]benzoic acid was obtained as white solid (9.8 g, 100%).

後処理

  1. customThe desired product was precipitated
  2. filtrationfiltered out
  3. customAfter being dried overnight

出典と根拠

ORDレコード
ord-d4cdc502fd844cb393bdfcf4550de3ac
出典データセット
uspto-grants-2010_01
特許番号
US07645771B2

関連ノート

読み込み中…