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Acetic Acid → 3-Acetamido-2-phenylpyrazolo[1,5-a]pyridine

HRID 1534128
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반응식

HRID 1534128 반응식
[N:1]([C:3]1[C:4]([C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=2)=[N:5][N:6]2[CH:11]=[CH:10][CH:9]=[CH:8][C:7]=12)=O.C(=O)(O)[O-].[Na+].[C:23](O)(=[O:25])[CH3:24]>[Zn]>[C:23]([NH:1][C:3]1[C:4]([C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=2)=[N:5][N:6]2[CH:11]=[CH:10][CH:9]=[CH:8][C:7]=12)(=[O:25])[CH3:24]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 176Acetic AcidHCID 516892Sodium BicarbonateHCID 143735903-Nitroso-2-phenylpyrazolo[1,5-a]pyridine

생성물 1

HCID 190924173-Acetamido-2-phenylpyrazolo[1,5-a]pyridine

시약·촉매·용매 1

HCID 23994Zinc촉매

실험 절차

A mixture of 3-nitroso-2-phenylpyrazolo[1,5-a]pyridine (0.81 g) and zinc powder (0.95 g) in acetic acid (10 ml) was heated under reflux for 2.5 hours. The reaction mixture was poured onto ice-water (100 ml) and neutralized with saturated aqueous sodium bicarbonate solution. Resultant precipitates were collected by filtration, washed with water, and recrystallized from ethyl acetate to give crystals of 3-acetamido-2-phenylpyrazolo[1,5-a]pyridine (304 mg).

후처리

  1. temperaturewas heated
  2. temperatureunder reflux for 2.5 hours
  3. additionThe reaction mixture was poured onto ice-water (100 ml)
  4. customResultant precipitates
  5. filtrationwere collected by filtration
  6. washwashed with water
  7. customrecrystallized from ethyl acetate

출처 및 근거

ORD 기록
ord-51d175e43cc64d1196e4f81f8e6b98d1
출처 데이터셋
uspto-grants-1992_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05087629

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