반응 #1755518

ord-4d5d4efd8a634b739b97bb363588779b

반응 방정식

Nc1cccc(C=O)c1
3-aminobenzaldehyde
O=C=Nc1cc(C(F)(F)F)ccc1F
2-fluoro-5-trifluoromethylphenyl isocyanate
O=S(=O)([O-])O.[K+]
potassium hydrogen sulfate
O=Cc1cccc(NC(=O)Nc2cc(C(F)(F)F)ccc2F)c1
aldehyde
수율 57.0%
O=Cc1cccc(NC(=O)Nc2cc(C(F)(F)F)ccc2F)c1
1-(2-fluoro-5-trifluoromethylphenyl)-3-(3-formylphenyl)urea
수율 57.0%

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    workup.ADDITIONis treated in a CEM Discover microwave oven at 100° C. for 10 minutes (power 90)
  2. 2
    온도After cooling
  3. 3
    추출extracted with twice 50 ml of ethyl acetate
  4. 4
    세척The combined organic phases are washed with water
  5. 5
    건조dried over sodium sulfate
  6. 6
    기타evaporated

실험 절차

A mixture of 484 mg of 3-aminobenzaldehyde (4 mmol) (polymerized form) and 290 μl of 2-fluoro-5-trifluoromethylphenyl isocyanate in 4 ml of DCE is treated in a CEM Discover microwave oven at 100° C. for 10 minutes (power 90). After cooling, the mixture is poured into 100 ml of saturated potassium hydrogen sulfate solution and extracted with twice 50 ml of ethyl acetate. The combined organic phases are washed with water, dried over sodium sulfate and evaporated. 740 mg of the expected aldehyde (yield=57%) are obtained in an LC/MS purity of 82%. The crude product is used directly for the following steps. ([M+H]+): 327. RT=4.28 min (acetonitrile/water gradient from 30% to 90%—Method B).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07989439B2uspto-grants-2011_08