Sodium Hydroxide → 3-Amino-6-(2,4-dichloro-phenyl)-5-trifluoromethyl-pyridine-2-carboxylic acid

HRID 444937ノート

反応式

HRID 444937 の反応式
C[O:2][C:3]([C:5]1[C:10]([NH2:11])=[CH:9][C:8]([C:12]([F:15])([F:14])[F:13])=[C:7]([C:16]2[CH:21]=[CH:20][C:19]([Cl:22])=[CH:18][C:17]=2[Cl:23])[N:6]=1)=[O:4].[OH-].[Na+].O1CCOCC1>CO>[NH2:11][C:10]1[C:5]([C:3]([OH:4])=[O:2])=[N:6][C:7]([C:16]2[CH:21]=[CH:20][C:19]([Cl:22])=[CH:18][C:17]=2[Cl:23])=[C:8]([C:12]([F:13])([F:14])[F:15])[CH:9]=1

参加物

5

実験手順

3-Amino-6-(2,4-dichloro-phenyl)-5-trifluoromethyl-pyridine-2-carboxylic acid methyl ester (0.9 g, 2.465 mmol) was suspended in MeOH (15 ml) and NaOH 2M (2.465 ml, 4.93 mmol) was added under stirring. 1,4-Dioxane (15.00 ml) was added and the solution was left standing at RT over night. The solvent was removed in vacuo and the resulting residue was dissolved in water (10 ml) and carefully acidified to pH4 with slow addition of 2M HCl (2 ml) whilst stirring. The mixture was extracted with EtOAc (20 ml) and the organic portion was washed with brine and concentrated in vacuo. The residue was purified by reverse phase chromatography (130 g C18 column) eluting with water/MeOH to afford the title compound; LS-MS Rt=1.57 mins [M+H]+ 351.0 (Method 2 min LC_v002).

後処理

  1. waitthe solution was left
  2. waitstanding at RT over night
  3. customThe solvent was removed in vacuo
  4. dissolutionthe resulting residue was dissolved in water (10 ml)
  5. additioncarefully acidified to pH4 with slow addition of 2M HCl (2 ml)
  6. stirringwhilst stirring
  7. extractionThe mixture was extracted with EtOAc (20 ml)
  8. washthe organic portion was washed with brine
  9. concentrationconcentrated in vacuo
  10. customThe residue was purified by reverse phase chromatography (130 g C18 column)
  11. washeluting with water/MeOH

出典と根拠

ORDレコード
ord-42b82da000714c8fbd726f709ccce3c2
出典データセット
uspto-grants-2013_07
特許番号
US08476269B2

反応ノート

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