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

HRID 731734
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HRID 731734 반응식
[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]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

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

생성물 1

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

시약·촉매·용매 2

HCID 962Water용매HCID 8028
Tetrahydrofuran
용매

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-11e85c5f963f4f1b97409560ea22af2f
출처 데이터셋
uspto-grants-2009_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07585875B2

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