Réaction #1509592

ord-09c60ed909ab4da4b35ee6add0eea841

Équation de réaction

CCOC(=O)c1cc(-c2nnnn2C)cc([N+](=O)[O-])c1
3-(1-Methyl-1H-tetrazol-5-yl)-5-nitro-benzoic acid ethyl ester
CCOC(=O)c1cc(N)cc(-c2nnnn2C)c1
title compound
Rendement 72.5%
CCOC(=O)c1cc(N)cc(-c2nnnn2C)c1
3-Amino-5-(1-methyl-1H-tetrazol-5-yl)-benzoic acid ethyl ester
Rendement 72.5%

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Autrewas hydrogenated at 20° C.
  2. 2
    AutreAfter reaction completion
  3. 3
    Filtrationthe mixture was filtered
  4. 4
    Concentrationthe filtrate concentrated in vacuum

Mode opératoire

A solution of 3-(1-Methyl-1H-tetrazol-5-yl)-5-nitro-benzoic acid ethyl ester (6.5 g) in EtOAc:ethanol (1:1, 320 ml) was hydrogenated at 20° C. and 50 psi with 10% Pd/C (750 mg). After reaction completion, the mixture was filtered and the filtrate concentrated in vacuum to give the title compound (4.2 g). Rt=1.21 min (method D).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: USRE045323E1uspto-grants-2015_01