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

HRID 2357911
ノート
印刷プレビュー

反応式

HRID 2357911 の反応式
[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
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

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

生成物 1

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

試薬・触媒・溶媒 1

HCID 679Dimethyl Sulfoxide溶媒

実験手順

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).

後処理

  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

出典と根拠

ORDレコード
ord-565902a8da2043ef8f0bd277bd280e60
出典データセット
uspto-grants-2010_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07763617B2

反応ノート

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