반응 #45644

ord-2275dce721af45a0b6e38967e634410c

반응 방정식

C[Si](C)(C)C=[N+]=[N-]
trimethylsilyldiazomethane
O
water
F[B-](F)(F)F.[H+]
tetrafluoroboric acid
F[B-](F)(F)F.[H+]
tetrafluoroboric acid
C[Si](C)(C)C=[N+]=[N-]
trimethylsilyldiazomethane
Cc1c(Br)c(F)c2oc(C(C)(C)CO)nc2c1C#N
6-Bromo-7-fluoro-2-(2-hydroxy-1,1-dimethylethyl)-5-methyl-1,3-benzoxazole-4-carbonitrile
COCC(C)(C)c1nc2c(C#N)c(C)c(Br)c(F)c2o1
compound
수율 106.1%
COCC(C)(C)c1nc2c(C#N)c(C)c(Br)c(F)c2o1
6-Bromo-2-[2-methoxy-1,1-dimethylethyl]-7-fluoro-5-methyl-1,3-benzoxazole-4-carbonitrile
수율 106.1%

반응 조건

온도
0°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    workup.ADDITIONwere dropwise added
  2. 2
    workup.STIRRINGby stirring for 19 hours
  3. 3
    온도with heating up to room temperature
  4. 4
    기타After the reaction
  5. 5
    기타the two reaction solutions
  6. 6
    추출followed by extraction with ethyl acetate
  7. 7
    세척washing with saturated brine
  8. 8
    건조The obtained organic layer was dried over anhydrous sodium sulfate
  9. 9
    기타the solvent was evaporated away under reduced pressure
  10. 10
    세척eluted with a mixed solvent of n-hexane/ethyl acetate (10:1

실험 절차

6-Bromo-7-fluoro-2-(2-hydroxy-1,1-dimethylethyl)-5-methyl-1,3-benzoxazole-4-carbonitrile (I-108) (912.6 mg, 2.79 mmol) and (514 mg, 1.57 mmol) were separately dissolved in methylene chloride (9 ml and 5 ml), and aqueous 42% tetrafluoroboric acid solution (420 μl, 2.79 mmol) and (240 μl, 1.57 mmol) were individually added to each, then with cooling with ice, trimethylsilyldiazomethane (2 M hexane solution, 2.8 ml, 5.58 mmol) and (1.6 ml, 3.14 mmol) were dropwise added, followed by stirring at 0° C. for 40 minutes; but since the reaction did not finish, the same amount of aqueous 42% tetrafluoroboric acid solution and trimethylsilyldiazomethane were added, followed by stirring for 19 hours with heating up to room temperature. After the reaction, the two reaction solutions were combined, water was added, followed by extraction with ethyl acetate and washing with saturated brine. The obtained organic layer was dried over anhydrous sodium sulfate, the solvent was evaporated away under reduced pressure. The resulting residue was subjected to silica gel column chromatography, and eluted with a mixed solvent of n-hexane/ethyl acetate (10:1, v/v) to obtain the entitled compound (1.01 g, 68%) as a white solid.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07737166B2uspto-grants-2010_06