Réaction #1605807

ord-d188d45e572842dc9e350cd84e47f770

Équation de réaction

CN1CCC(OC(=O)Nc2cc(CCCC(=O)OCc3ccccc3)ccc2-c2ccccc2)CC1
Benzyl 4-[3-({[(1-methylpiperidin-4-yl)oxy]carbonyl}amino)-4-phenylphenyl]butyrate
CN1CCC(OC(=O)Nc2cc(CCCC(=O)O)ccc2-c2ccccc2)CC1
4-[3-({[(1-methylpiperidin-4-yl)oxy]carbonyl}amino)-4-phenylphenyl]butyric acid

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    workup.WAITat 50° C. for 6 hours
  2. 2
    FiltrationAfter filtering the reaction solution through celite
  3. 3
    Concentrationthe filtrate was concentrated under reduced pressure

Mode opératoire

Benzyl 4-[3-({[(1-methylpiperidin-4-yl)oxy]carbonyl}amino)-4-phenylphenyl]butyrate (25.8 g, 5.30 mmol) was dissolved in ethyl acetate (250 mL), 10% palladium hydroxide-carbon (5 g) was added thereto, and the mixture was stirred under a hydrogen atmosphere at room temperature for 3 days and, thereafter, at 50° C. for 6 hours. After filtering the reaction solution through celite, the filtrate was concentrated under reduced pressure to obtain 4-[3-({[(1-methylpiperidin-4-yl)oxy]carbonyl}amino)-4-phenylphenyl]butyric acid (21.3 g).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US09072734B2uspto-grants-2015_07