Phosphorus oxychloride → 7-[3-(Trifluoromethyl)phenyl]pyrazolo[1,5-a]pyrimidine-3-carbonitrile

HRID 225275

반응식

HRID 225275 반응식
[F:1][C:2]([F:22])([F:21])[C:3]1[CH:8]=[CH:7][CH:6]=[C:5]([C:9]2[N:14]3[N:15]=[CH:16][C:17]([C:18]([NH2:20])=O)=[C:13]3[N:12]=[CH:11][CH:10]=2)[CH:4]=1.P(Cl)(Cl)(Cl)=O>>[F:21][C:2]([F:1])([F:22])[C:3]1[CH:8]=[CH:7][CH:6]=[C:5]([C:9]2[N:14]3[N:15]=[CH:16][C:17]([C:18]#[N:20])=[C:13]3[N:12]=[CH:11][CH:10]=2)[CH:4]=1

참가 물질

3

실험 절차

One gram of 7-(α,α,α-trifluoro-m-tolyl)pyrazolo[1,5-a]pyrimidine-3-carboxamide and 5 ml. of phosphorus oxychloride is refluxed for 3 hours. The reaction mixture is evaporated to dryness and the residue is dissolved in methylene chloride, washed with saturated sodium bicarbonate solution, dried with anhydrous sodium sulfate. After passing through a short pad of hydrous magnesium silicate with eluent methylene chloride. Concentration of the eluent with addition of n-hexane gives the product, m.p. 141°-143° C.

후처리

  1. customThe reaction mixture is evaporated to dryness
  2. dissolutionthe residue is dissolved in methylene chloride
  3. washwashed with saturated sodium bicarbonate solution
  4. dry with materialdried with anhydrous sodium sulfate
  5. additionConcentration of the eluent with addition of n-hexane
  6. customgives the product, m.p. 141°-143° C.

출처 및 근거

ORD 기록
ord-b6ae1a74f7da4a72b8218ea4820892f8
출처 데이터셋
uspto-grants-1980_11
특허 번호
US04236005

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