Reaktion #2300

ord-dec26e4a500a423b998283ba15ea943b

Reaktionsgleichung

COC(=O)Cc1ccc(C(=O)CCl)cc1
methyl 4-chloroacetylphenylacetate
c1cc(N2CCNCC2)ccn1
1-(4-pyridyl)piperazine
COC(=O)Cc1ccc(C(=O)CN2CCN(c3ccncc3)CC2)cc1
title compound
COC(=O)Cc1ccc(C(=O)CN2CCN(c3ccncc3)CC2)cc1
Methyl 4-[2-[4-(4-pyridyl)piperazin-1-yl]acetyl]-phenylacetate

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeThe supernatent was decanted from the solid
  2. 2
    Sonstigeformed
  3. 3
    Einengenconcentrated in vacuo
  4. 4
    Sonstigepurified by flash chromatography on neutral alumina
  5. 5
    Wascheneluting with dichloromethane

Vorschrift

A solution of methyl 4-chloroacetylphenylacetate (260 mg) in acetonitrile (4 ml) was added dropwise over 15 minutes to a stirred solution of 1-(4-pyridyl)piperazine (375 mg) in acetonitrile (10 ml) and the mixture stirred overnight. The supernatent was decanted from the solid formed, concentrated in vacuo and purified by flash chromatography on neutral alumina, eluting with dichloromethane then 0.25% v/v methanol/dichloromethane and finally 0.5% v/v methanol dichloromethane. Concentration of the fractions in vacuo gave the title compound, 96 mg, as a white crystalline solid: m.p. 127°-129° C.; NMR (d6 DMSO) δ 8.15(2H,d), 7.98(2H,d), 7.41(2H,d), 6.81(2H,d), 3.91(2H,s), 3.78(2H,s), 3.53(3H,s), 3.33(4H,t), 2.64(4H,t); m/e 354(M+H )+ ; calculated for C20H23N3O3 : C, 68.0; H, 6.6; N, 11.9. found: C, 68.2; H, 6.6; N, 11.9%.

Quelle

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