Potassium Hydroxide → 1,5-diamino-3-(4-fluorophenyl)-1H-pyrazole

HRID 902202노트

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HRID 902202 반응식
[NH2:1]OS(O)(=O)=O.[NH2:7][C:8]1[NH:12][N:11]=[C:10]([C:13]2[CH:18]=[CH:17][C:16]([F:19])=[CH:15][CH:14]=2)[CH:9]=1.[OH-].[K+]>>[NH2:1][N:12]1[C:8]([NH2:7])=[CH:9][C:10]([C:13]2[CH:18]=[CH:17][C:16]([F:19])=[CH:15][CH:14]=2)=[N:11]1

참가 물질

4

반응물 3

HCID 14797Potassium Hydroxide2회HCID 76284hydroxylamine-O-sulfonic acid2회HCID 178507289HCID 178507289, 화합물

생성물 1

HCID 230848951,5-diamino-3-(4-fluorophenyl)-1H-pyrazole수율 14.9%

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온도
80 °C

실험 절차

Hydroxylamine-O-sulfonic acid (2.26 g, 20.0 mmol) was portionwise added to aqueous solution (100 mL) containing 5-amino-3-(4-fluorophenyl)-1H-pyrazole (2.0 g, 11.3 mmol) and potassium hydroxide (2.52 g, 45 mmol) while stirring at 80° C. After the mixture was stirred at 80° C. for 30 minutes, potassium hydroxide (2.52 g, 45 mmol) was added thereto, hydroxylamine-O-sulfonic acid (2.26 g, 20.0 mmol) was portionwise added, and the mixture was stirred for further 1 hour. The reaction solution was cooled down to room temperature, and extracted with ethyl acetate. The organic layer was washed with saturated brine, dried over anhydrous potassium carbonate, and concentrated in vacuo. The residue was purified by a silica gel column chromatography (C-300, hexane:ethyl acetate=1:2) to obtain the title compound (324 mg, 14.9%).

후처리

  1. stirringAfter the mixture was stirred at 80° C. for 30 minutes
  2. stirringthe mixture was stirred for further 1 hour
  3. temperatureThe reaction solution was cooled down to room temperature
  4. extractionextracted with ethyl acetate
  5. washThe organic layer was washed with saturated brine
  6. dry with materialdried over anhydrous potassium carbonate
  7. concentrationconcentrated in vacuo
  8. customThe residue was purified by a silica gel column chromatography (C-300, hexane:ethyl acetate=1:2)

출처 및 근거

ORD 기록
ord-4131979826d2487cbb0c59bb833e4b86
출처 데이터셋
uspto-grants-2008_04
특허 번호
US07365079B2

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