반응 #46904

ord-efdd765be6a748e18147c7442f20519c

반응 방정식

NC(=O)c1ccc(O)cc1
4-hydroxybenzamide
O=C(O)Cc1ccccc1Nc1c(Cl)cccc1Cl
diclofenac
Oc1cccc2[nH]nnc12
hydroxybenzotriazole
C(=NC1CCCCC1)=NC1CCCCC1
DCC
NC(=O)c1ccc(OC(=O)Cc2ccccc2Nc2c(Cl)cccc2Cl)cc1
4-carbamoylphenyl 2-[2-(2,6-dichlorophenylamino)-phenyl]acetate
수율 17.0%

반응 조건

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

후처리

  1. 1
    workup.STIRRINGstirred for 1 h at 0° C.
  2. 2
    기타at room temperature
  3. 3
    여과After filtration
  4. 4
    기타the filtrate was evaporated under reduced pressure
  5. 5
    기타the oily residue thus obtained
  6. 6
    세척the organic layer was washed with brine
  7. 7
    건조dried on anhydrous MgSO4
  8. 8
    여과filtered
  9. 9
    기타the solvent evaporated
  10. 10
    세척eluted with CH2Cl2/MeOH (9/1), from which 4-carbamoylphenyl 2-(2-(2,6-dichlorophenylamino)phenyl)acetate (5)
  11. 11
    기타was obtained (212 mg, 17% yield)

실험 절차

To the solution of 1 (diclofenac, 890 mg, 3.0 mmol) in 50 mL of N,N-dimethylformamide, hydroxybenzotriazole (445 mg, 3.3 mmol) and DCC (680 mg, 3.3 mmol) were added with stirring at 0° C. for 1 h. To the reaction mixture 4-hydroxybenzamide (4, 616 mg, 4.5 mmol) was added and stirred for 1 h at 0° C. and 3 hs at room temperature. After filtration, the filtrate was evaporated under reduced pressure and the oily residue thus obtained was dissolved in chloroform; the organic layer was washed with brine, dried on anhydrous MgSO4, filtered and the solvent evaporated. The crude product 5 was loaded on a silica gel open column and eluted with CH2Cl2/MeOH (9/1), from which 4-carbamoylphenyl 2-(2-(2,6-dichlorophenylamino)phenyl)acetate (5) was obtained (212 mg, 17% yield).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07741359B2uspto-grants-2010_06