Reaktion #2316

ord-e33d3c2da1e849fdb7d26db578a0da09

Reaktionsgleichung

COC(=O)COc1ccc(C(=O)CN2CCN(c3ccncc3)CC2)cc1
product
COC(=O)COc1ccc(C(=O)CN2CCN(c3ccncc3)CC2)cc1
Methyl 4-[2-[4-(4-pyridyl)piperazin-1-yl]acetyl]-phenoxyacetate
N
ammonia
NC(=O)COc1ccc(C(=O)CN2CCN(c3ccncc3)CC2)cc1
title compound
NC(=O)COc1ccc(C(=O)CN2CCN(c3ccncc3)CC2)cc1
4-[2-[4-(4-Pyridyl)piperazin-1-yl]acetyl]phenoxy-acetamide

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigesealed in a pressure bottle
  2. 2
    SonstigeThe orange crystals which formed
  3. 3
    Filtrationafter filtration
  4. 4
    Waschenwashing with a little methanol

Vorschrift

A solution of the product of Example 1 (200 mg) in methanol (10 ml), prepared under argon, was cooled to 4° C. and saturated with dry ammonia gas, then sealed in a pressure bottle and kept for 2 days. The orange crystals which formed, after filtration and washing with a little methanol, gave the title compound, 140 mg: m.p. 247° to 248° C.; NMR (d6DMSO) δ 8.16 (2H, d), 7.99 (2H, d), 7.55 (1H, bs), 7.37 (1H, bs), 7.02 (2H, d), 6.81 (2H, d), 4.54 (2H, s), 3.85 (2H, s), 3.33 (4H, t), 2.60 (4H, t); m/e 355 (M+H)+ ; calculated for C19 H22N4O3 : C, 64.4; H, 6.3; N, 15.8. found: C, 64.4; H, 6.4; N, 15.6%.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05728701uspto-grants-1998_03