Reaktion #1149986

ord-4810610c3e7a47a48a5fc640b37872ea

Reaktionsgleichung

[Cl-].[NH4+]
ammonium chloride
CC(=O)OCCOc1nn(C)c(N)c1-c1ccc2c(c1)OCO2
2-{[5-amino-4-(1,3-benzodioxol-5-yl)-1-methyl-1H-pyrazol-3-yl]oxy}ethyl acetate
[Na]
sodium
Cn1nc(OCCO)c(-c2ccc3c(c2)OCO3)c1N
title compound
Ausbeute 97.9%
Cn1nc(OCCO)c(-c2ccc3c(c2)OCO3)c1N
2-{[5-amino-4-(1,3-benzodioxol-5-yl)-1-methyl-1H-pyrazol-3-yl]oxy}-1-ethanol
Ausbeute 97.9%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    ExtraktionThe mixture was extracted with ethyl acetate (3×6 ml)
  2. 2
    TrocknenThe organic fraction was dried over sodium sulfate
  3. 3
    Einengenconcentrated under reduced pressure

Vorschrift

To a solution of 2-{[5-amino-4-(1,3-benzodioxol-5-yl)-1-methyl-1H-pyrazol-3-yl]oxy}ethyl acetate (100 mg) (Preparation 33) in ethanol (6 ml) at room temperature, was added sodium hydroxyde (100 mg). After one hour, the reaction was diluted with water (5 ml) and an aqueous saturated solution of ammonium chloride (10 ml). The mixture was extracted with ethyl acetate (3×6 ml). The organic fraction was dried over sodium sulfate and concentrated under reduced pressure to yield the title compound as a white solid (85 mg).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US06962923B2uspto-grants-2005_11