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Triethylamine → 7-Methoxy-4-propionyl-2-trifluoromethyl-pyrazolo[1,5-a]pyridine

HRID 2357911
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인쇄 미리보기

반응식

HRID 2357911 반응식
[OH:1][CH:2]([C:5]1[C:6]2[N:7]([N:13]=[C:14]([C:16]([F:19])([F:18])[F:17])[CH:15]=2)[C:8]([O:11][CH3:12])=[CH:9][CH:10]=1)[CH2:3][CH3:4].C(N(CC)CC)C>CS(C)=O>[CH3:12][O:11][C:8]1[N:7]2[N:13]=[C:14]([C:16]([F:19])([F:17])[F:18])[CH:15]=[C:6]2[C:5]([C:2](=[O:1])[CH2:3][CH3:4])=[CH:10][CH:9]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 8471TriethylamineHCID 593893854-(1-Hydroxypropyl)-7-methoxy-2-trifluoromethyl-pyrazolo[1,5-a]pyridine

생성물 1

HCID 593893617-Methoxy-4-propionyl-2-trifluoromethyl-pyrazolo[1,5-a]pyridine수율 75.3%

시약·촉매·용매 1

HCID 679Dimethyl Sulfoxide용매

실험 절차

The compound of Example 135 (32.1 g) was dissolved in DMSO (780 mL) in an argon atmosphere. To this solution, triethylamine (163 mL) and sulfur trioxide-pyridine complex (93.1 g) were sequentially added and the mixture was stirred at room temperature for 1 hour. The reaction mixture was then poured into ice water and the resulting solid product was collected by filtration. The product was washed with water and dissolved in ethyl acetate. The solution was dried over anhydrous sodium sulfate. Evaporation of the solvent afforded the title compound as a colorless powder (24.0 g).

후처리

  1. filtrationthe resulting solid product was collected by filtration
  2. washThe product was washed with water
  3. dissolutiondissolved in ethyl acetate
  4. dry with materialThe solution was dried over anhydrous sodium sulfate
  5. customEvaporation of the solvent

출처 및 근거

ORD 기록
ord-565902a8da2043ef8f0bd277bd280e60
출처 데이터셋
uspto-grants-2010_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07763617B2

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