Reacción #2045050

ord-8f48782a75f947b0928a27e00baa35d7

Ecuación de reacción

O=C(Cl)COCc1ccccc1
Benzyloxyacetyl chloride
COC(=O)CCCCCOc1ccc(N)cc1
6-(4-aminophenoxy)hexanoic acid methyl ester
COC(=O)CCCCCOc1ccc(N)cc1
6-(4-Amino-phenoxy)-hexanoic acid methyl ester
CCN(CC)CC
triethylamine
COC(=O)CCCCCOc1ccc(NC(=O)COCc2ccccc2)cc1
70
Rendimiento 22.2%
COC(=O)CCCCCOc1ccc(NC(=O)COCc2ccccc2)cc1
6-[4-(2-Benzyloxyacetylamino)phenoxy]hexanoic acid methyl ester
Rendimiento 22.2%

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    FiltraciónSolids were filtered off
  2. 2
    workup.DISTILLATIONacetone distilled off
  3. 3
    workup.ADDITIONwater (100 ml) added
  4. 4
    ExtracciónCrude 70 was extracted into chloroform
  5. 5
    Lavadowashed with 5% sodium bicarbonate solution (2×100 ml), water (100 ml)
  6. 6
    Secadodried over sodium sulphate
  7. 7
    workup.DISTILLATIONdistilled
  8. 8
    OtroCrude 70 was purified by column chromatography on silica gel

Procedimiento

Benzyloxyacetyl chloride (25 gm, 135.5 mmol) was added dropwise to a mixture of 6-(4-aminophenoxy)hexanoic acid methyl ester 21 (25 g, 105 mmol) and triethylamine (21.4 g, 211.6 mmol) in acetone (200 ml) at 0° C. and stirred at room temp. for 12 hrs. Solids were filtered off, acetone distilled off and water (100 ml) added. Crude 70 was extracted into chloroform, washed with 5% sodium bicarbonate solution (2×100 ml), water (100 ml), dried over sodium sulphate and distilled. Crude 70 was purified by column chromatography on silica gel using benzene as eluant to get pure 70 (9 g, 22.2%) as a off-white powder. M.p: 46-49° C.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08409559B2uspto-grants-2013_04