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

HRID 1059705

反応式

HRID 1059705 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 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 water, dried over Na2SO4 and concentrated in vacuo to give (5-(1-hydroxy-1-methyl-ethyl))-pyridine-2-sulfonic acid amide as yellow oil. El 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 with water
  4. dry with materialdried over Na2SO4
  5. concentrationconcentrated in vacuo

出典と根拠

ORDレコード
ord-1e5674e319b44f52a4b76356230af6f2
出典データセット
uspto-grants-2003_02
特許番号
US06521631B2

関連ノート

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