Reaktion #1455842

ord-69de71fae24144ba8b22328d74832713

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 (10 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: US06573270B1uspto-grants-2003_06