Hydrochloric Acid → (5-(1-Hydroxy-1-methyl-ethyl))-pyridine-2-sulfonic acid amide

HRID 1066505

反応式

HRID 1066505 の反応式
[K+].[CH:2]([C:5]1[CH:6]=[CH:7][C:8]([S:11]([NH-:14])(=[O:13])=[O:12])=[N:9][CH:10]=1)([CH3:4])[CH3:3].[O-:15][Mn](=O)(=O)=O.[K+].Cl>O>[OH:15][C:2]([C:5]1[CH:6]=[CH:7][C:8]([S:11]([NH2:14])(=[O:13])=[O:12])=[N:9][CH:10]=1)([CH3:4])[CH3:3]

参加物

5

反応物 3

HCID 313Hydrochloric AcidHCID 516875Potassium PermanganateHCID 1317209445-Isopropyl pyridine-2-sulfonamide potassium salt

生成物 1

HCID 54360667(5-(1-Hydroxy-1-methyl-ethyl))-pyridine-2-sulfonic acid amide

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

To a solution of 5-isopropyl-pyridine-2-sulfonamide potassium salt (synthesis described in EP 0 799 209) in water (10 ml) were added 1.2 g of KMnO4 at RT and the mixture was then refluxed for 30 minutes. The mixture was cooled to RT, acidified with diluted HCl and the product was extracted into AcOEt. The organic layer was washed with washed with water, dried over Na2SO4 and concentrated in vacuo to give (5-(1-hydroxy-1-methyl-ethyl))-pyridine-2-sulfonic acid amide as yellow oil. EI mass spectrum, m/e 216 (M calculated for: C8H12N2O3S 216).

後処理

  1. temperaturethe mixture was then refluxed for 30 minutes
  2. extractionthe product was extracted into AcOEt
  3. washThe organic layer was washed
  4. washwith washed with water
  5. dry with materialdried over Na2SO4
  6. concentrationconcentrated in vacuo

出典と根拠

ORDレコード
ord-c31ba97edaf847d8a81e22851e037264
出典データセット
uspto-grants-2001_06
特許番号
US06242601B1

関連ノート

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