반응 #312446

ord-2e0c48f276d2478581c796f80821424e

반응 방정식

O=C(O)c1cnn2c(-c3cccc(C(F)(F)F)c3)ccnc12
7-(α,α,α-trifluoro-m-tolyl)pyrazolo[1,5-a]pyrimidine-3-carboxylic acid
B#B
diborane
Cc1cnn2c(-c3cccc(C(F)(F)F)c3)ccnc12
3-Methyl-7-(α,α,α-trifluoro-m-tolyl)pyrazolo[1,5-a]pyrimidine

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    workup.ADDITIONthe mixture is poured onto ice
  2. 2
    추출the product extracted into dichloromethane
  3. 3
    세척The dichloromethane layer is washed with water
  4. 4
    건조dried (MgSO4)
  5. 5
    기타the solvent removed
  6. 6
    기타to give the product of the example

실험 절차

A solution of 0.01 mole of 7-(α,α,α-trifluoro-m-tolyl)pyrazolo[1,5-a]pyrimidine-3-carboxylic acid in tetrahydrofuran is added dropwise to a chilled (0° C.) solution of 0.02 mole of diborane in tetrahydrofuran. After standing overnight the mixture is poured onto ice and the product extracted into dichloromethane. The dichloromethane layer is washed with water, dried (MgSO4) and the solvent removed to give the product of the example.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US04236005uspto-grants-1980_11