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Sulfuric Acid → 3-Cyclopropylamino-2-methyl-4-(methylsulfonyl)benzoic acid

HRID 548524
ノート
印刷プレビュー

反応式

HRID 548524 の反応式
F[C:2]1[C:3]([CH3:15])=[C:4]([CH:8]=[CH:9][C:10]=1[S:11]([CH3:14])(=[O:13])=[O:12])[C:5]([OH:7])=[O:6].[CH:16]1([NH2:19])[CH2:18][CH2:17]1.S(=O)(=O)(O)O>>[CH:16]1([NH:19][C:2]2[C:3]([CH3:15])=[C:4]([CH:8]=[CH:9][C:10]=2[S:11]([CH3:14])(=[O:13])=[O:12])[C:5]([OH:7])=[O:6])[CH2:18][CH2:17]1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

4

反応物 3

HCID 1118Sulfuric AcidHCID 69828CyclopropylamineHCID 142544793-Fluoro-2-methyl-4-(methylsulfonyl)benzoic acid

生成物 1

HCID 574249453-Cyclopropylamino-2-methyl-4-(methylsulfonyl)benzoic acid

反応条件

温度
120 °C

実験手順

5.0 g (22 mmol) of 3-fluoro-2-methyl-4-(methylsulfonyl)benzoic acid were dissolved in 25.0 ml (356 mmol) of cyclopropylamine. With stirring, the mixture was then heated in an autoclave at 120° C. for 1 day, and then cooled to room temperature (RT), acidified with a mixture of ice-water and conc. sulfuric acid and extracted with ethyl acetate. The combined organic phases were dried over MgSO4, and the solvent was removed under reduced pressure. The residue was purified by preparative HPLC. This gave 1.8 g of a beige solid of purity of 95%.

後処理

  1. temperaturecooled to room temperature (RT)
  2. extractionextracted with ethyl acetate
  3. dry with materialThe combined organic phases were dried over MgSO4
  4. customthe solvent was removed under reduced pressure
  5. customThe residue was purified by preparative HPLC

出典と根拠

ORDレコード
ord-dbb00001c4bc416dac27fb72a49e131f
出典データセット
uspto-grants-2011_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07943550B2

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート