Reacción #2045026

ord-629d7deee69740c19b82f28d4ed1ae96

Ecuación de reacción

COC(=O)CCCCCOc1ccc(NC(=O)OCCO)cc1
6-[4-(2-Hydroxyethoxycarbonylamino)phenoxy]hexanoic acid methyl ester
COC(=O)CCCCCOc1ccc(NC(=O)OCCO)cc1
6-[4-(2-Hydroxy-ethoxycarbonylamino)-phenoxy]-hexanoic acid methyl ester
COC(=O)CCCCCOc1ccc(N=C=O)cc1
6-(4-Isocyanatophenoxy)hexanoic acid methyl ester
COC(=O)CCCCCOc1ccc(N=C=O)cc1
6-(4-Isocyanato-phenoxy)-hexanoic acid methyl ester
COC(=O)CCCCCOc1ccc(NC(=O)OCCOC(=O)Nc2ccc(OCCCCCC(=O)OC)cc2)cc1
38
Rendimiento 95.0%
COC(=O)CCCCCOc1ccc(NC(=O)OCCOC(=O)Nc2ccc(OCCCCCC(=O)OC)cc2)cc1
6-(4-{2-[4-(5-Methoxycarbonyl-pentyloxy)-phenylcarbamoyloxy]-ethoxycarbonylamino}-phenoxy)-hexanoic acid methyl ester
Rendimiento 95.0%

Disolventes

Condiciones de reacción

Temperatura
60°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    workup.DISTILLATIONToluene was distilled off
  2. 2
    workup.ADDITIONwater (50 ml) was added
  3. 3
    FiltraciónThe solid was filtered
  4. 4
    Otrodried
  5. 5
    Otroto give crude 38, which
  6. 6
    Otrowas purified by column chromatography on silica gel

Procedimiento

To a mixture of 6-[4-(2-Hydroxyethoxycarbonylamino)phenoxy]hexanoic acid methyl ester 37 (5 g, 15.38 mmol) in toluene (50 ml) was added 6-(4-Isocyanatophenoxy)hexanoic acid methyl ester 36 (4 g, 15.2 mmol) at room temperature and heated to 60° C. for 2 hours. Toluene was distilled off and water (50 ml) was added. The solid was filtered and dried to give crude 38, which was purified by column chromatography on silica gel using chloroform as eluant to get pure 38 (8.5 g, 94%) as a white powder. M.p: 118-120.5° C.

Fuente

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