Reaktion #2301

ord-77e50f1da1444b07b851d442f07f91b1

Reaktionsgleichung

CCC(=O)c1ccc(OCC(=O)OC)cc1
methyl 4-(2-methylacetyl)phenoxyacetate
c1cc(N2CCNCC2)ccn1
1-(4-pyridyl)piperazine
COC(=O)COc1ccc(C(=O)C(C)N2CCN(c3ccncc3)CC2)cc1
title compound
COC(=O)COc1ccc(C(=O)C(C)N2CCN(c3ccncc3)CC2)cc1
Methyl 4-[2-[4-(4-pyridyl)piperazin-1-yl]-2-methyl-acetyl]phenoxyacetate

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    FiltrationThe mixture was then filtered
  2. 2
    Sonstigethe filtrate evaporated
  3. 3
    Sonstigeto give an oil
  4. 4
    SonstigePurification by flash chromatography
  5. 5
    Wascheneluting first with dichloromethane

Vorschrift

A solution of RS methyl 4-(2-methylacetyl)phenoxyacetate (1.2 g) in acetonitrile (10 ml) was added dropwise over 30 minutes to a stirred solution of 1-(4-pyridyl)piperazine (1.3 g) in acetonitrile (30 ml) and the mixture stirred overnight. The mixture was then filtered and the filtrate evaporated to give an oil. Purification by flash chromatography, eluting first with dichloromethane then successively 2.5%, 3%, 4%, 5% and 10% v/v methanol/dichloromethane gave the title compound, 220 mg as a solid: m.p. 81°-83° C.; NMR (d6DMSO) δ 8.13(2H,d), 8.06(2H,d), 7.02(2H,d), 6.77(2H,d), 4.92(2H,s), 4.33(1H,q), 3.72(3H,s), 3.26(4H,t), 2.63(4H,t), 1.16(3H,d); m/e 384(M+H)+ ; calculated for C21H25N3O4 : C, 65.8; H, 6.6; N, 11.0. found C, 65.7; H, 6.8; N, 10.9%.

Quelle

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