Acetic Acid → 5-Hydroxy-2-((2-methyl-3-(trifluoromethyl)phenyl)amino)-3-pyridinecarboxylic acid

HRID 1395648

反応式

HRID 1395648 の反応式
[CH3:1][C:2]1[C:17]([C:18]([F:21])([F:20])[F:19])=[CH:16][CH:15]=[CH:14][C:3]=1[NH:4][C:5]1[N:13]=[CH:12][CH:11]=[CH:10][C:6]=1[C:7]([OH:9])=[O:8].C(O)(=[O:24])C.OO>O>[OH:24][C:11]1[CH:12]=[N:13][C:5]([NH:4][C:3]2[CH:14]=[CH:15][CH:16]=[C:17]([C:18]([F:19])([F:21])[F:20])[C:2]=2[CH3:1])=[C:6]([CH:10]=1)[C:7]([OH:9])=[O:8]

参加物

5

反応物 3

HCID 176Acetic AcidHCID 784Hydrogen Peroxide2 回HCID 38081Flunixin

生成物 1

HCID 129782155-Hydroxy-2-((2-methyl-3-(trifluoromethyl)phenyl)amino)-3-pyridinecarboxylic acid

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

To a suspension of 10 g. of 2-(2-methyl-3-trifluoromethylanilino) nicotinic acid and 160 ml. of glacial acetic acid, add 9 ml. of 30% hydrogen peroxide solution at room temperature. Warm the reaction mixture on a steam bath for one hour and add an additional 5 ml. of 30% hydrogen peroxide. Heat the resulting mixture for three hours on a steam bath, dilute with water and filter. After recrystallization from acetic acid, the product, 5-hydroxy-2-(2-methyl-3-trifluoromethylanilino) nicotinic acid melts at 305°-308° (dec.)

後処理

  1. additionTo a suspension of 10 g
  2. customat room temperature
  3. temperatureWarm the reaction mixture on a steam bath for one hour
  4. additionadd an additional 5 ml
  5. temperatureHeat the resulting mixture for three hours on a steam bath
  6. filtrationfilter
  7. customAfter recrystallization from acetic acid

出典と根拠

ORDレコード
ord-d6cf29cb4a114fc897e812715c781ee1
出典データセット
uspto-grants-1980_05
特許番号
US04205073

関連ノート

読み込み中…