Hydrochloric Acid → 3-(Methoxymethyl)-7-(alpha,alpha,alpha-trifluoro-m-tolyl)pyrazolo[1,5-a]pyrimidine

HRID 1447907

반응식

HRID 1447907 반응식
[F:1][C:2]([F:21])([F:20])[C:3]1[CH:8]=[CH:7][CH:6]=[C:5]([C:9]2[N:14]3[N:15]=[CH:16][C:17]([CH:18]=[O:19])=[C:13]3[N:12]=[CH:11][CH:10]=2)[CH:4]=1.[BH4-].[Na+].Cl.[CH3:25]O>>[CH3:25][O:19][CH2:18][C:17]1[CH:16]=[N:15][N:14]2[C:9]([C:5]3[CH:4]=[C:3]([C:2]([F:20])([F:1])[F:21])[CH:8]=[CH:7][CH:6]=3)=[CH:10][CH:11]=[N:12][C:13]=12

참가 물질

5

실험 절차

A suspension of 1.35 g. of 7-(α,α,α-trifluoro-m-tolyl)pyrazolo[1,5-a]pyrimidine-3-carboxaldehyde in 90 ml. of absolute methanol is treated with 0.175 g. of sodium borohydride. After stirring for 2 hours at room temperature, excess 1 N aqueous hydrochloric acid is added and the mixture with the methanol is concentrated under reduced pressure. The solid that separates is dissolved in methylene chloride and this solution is washed with a saturated sodium bicarbonate solution and then dried (sodium sulfate). Addition of hexane to this refluxing solution causes the desired compound to crystallize, m.p. 114°-116° C.

후처리

  1. additionA suspension of 1.35 g
  2. concentrationthe mixture with the methanol is concentrated under reduced pressure
  3. dissolutionThe solid that separates is dissolved in methylene chloride
  4. washthis solution is washed with a saturated sodium bicarbonate solution
  5. dry with materialdried (sodium sulfate)
  6. additionAddition of hexane to this refluxing solution
  7. customto crystallize

출처 및 근거

ORD 기록
ord-0e054ec4299f4e18ab1ac7e51f81586c
출처 데이터셋
uspto-grants-1979_12
특허 번호
US04178449

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