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Potassium Hydroxide → 2-Isopropylpyrazolo[1,5-a]pyridine-3-carboxylic acid

HRID 731734
ノート
印刷プレビュー

反応式

HRID 731734 の反応式
[CH:1]([C:4]1[C:12]([CH:13]=[O:14])=[C:7]2[CH:8]=[CH:9][CH:10]=[CH:11][N:6]2[N:5]=1)([CH3:3])[CH3:2].[Mn]([O-])(=O)(=O)=[O:16].[K+].[OH-].[K+]>C1COCC1.O>[CH:1]([C:4]1[C:12]([C:13]([OH:16])=[O:14])=[C:7]2[CH:8]=[CH:9][CH:10]=[CH:11][N:6]2[N:5]=1)([CH3:3])[CH3:2]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 14797Potassium HydroxideHCID 516875Potassium PermanganateHCID 143032672-Isopropylpyrazolo[1,5-a]pyridine-3-carbaldehyde

生成物 1

HCID 578374592-Isopropylpyrazolo[1,5-a]pyridine-3-carboxylic acid収率 60.2%

試薬・触媒・溶媒 2

HCID 962Water溶媒HCID 8028
Tetrahydrofuran
溶媒

実験手順

A mixture of 2-isopropylpyrazolo[1,5-a]pyridine-3-carbaldehyde (1.5 g, 1 equivalent) and potassium permanganate (2.9 g, 2.1 equivalents) in 10 mL of THF was stirred at room temperature for 2 days. A solution of potassium hydroxide (2.2 g, 5 equivalents) in 10 mL of water was added and the resulting solution was stirred at room temperature for 2 hours. The mixture was filtered to remove insoluble solids and the filtrate was extracted to remove unreacted aldehyde. The remaining aqueous solution was acidified with concentrated HCl and the precipitates were collected by filtration and dried under reduced pressure to give 2-isopropylpyrazolo[1,5-a]pyridine-3-carboxylic acid (0.98 g, 60% yield) as a solid. Compound 1079.

後処理

  1. stirringthe resulting solution was stirred at room temperature for 2 hours
  2. filtrationThe mixture was filtered
  3. customto remove insoluble solids
  4. extractionthe filtrate was extracted
  5. customto remove unreacted aldehyde
  6. filtrationthe precipitates were collected by filtration
  7. customdried under reduced pressure

出典と根拠

ORDレコード
ord-11e85c5f963f4f1b97409560ea22af2f
出典データセット
uspto-grants-2009_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07585875B2

反応ノート

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