Reaktion #78177

ord-1966a47c283b44e685e6d94508d37553

Reaktionsgleichung

CC(c1ccncc1)c1n[nH]c(=O)c2ccccc12
rac 4-[1-(4-pyridyl)ethyl]-1(2H)-phthalazinone
O=P12OP3(=O)OP(=O)(O1)OP(=O)(O2)O3
phosphorus pentoxide
CCN(CC)CC.Cl
triethylamine hydrochloride
Nc1ccc(Cl)cc1
4-chloroaniline
CC(c1ccncc1)c1nnc(Nc2ccc(Cl)cc2)c2ccccc12
title compound
CC(c1ccncc1)c1nnc(Nc2ccc(Cl)cc2)c2ccccc12
rac 1-(4-Chloroanilino) 4-[1-(4-pyridyl)ethyl]phthalazine

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturis heated for 8 h to 205° C
  2. 2
    Waschenwashed successively with sat. Na2CO3 solution, 3× with water and brine
  3. 3
    Waschenthe organic phase (Na2O4) is washed
  4. 4
    Einengenconcentrated by evaporation

Vorschrift

A mixture of 300 mg (1.19 mmol) rac 4-[1-(4-pyridyl)ethyl]-1(2H)-phthalazinone, 683 mg (4.77 mmol) phosphorus pentoxide, 657 mg (4.77 mmol) triethylamine hydrochloride, and 609 mg (4.77 mmol) 4-chloroaniline is heated for 8 h to 205° C. The brown solution is taken up in dichloromethane/methanol 19:1, washed successively with sat. Na2CO3 solution, 3× with water and brine, and the organic phase (Na2O4) is washed and concentrated by evaporation. Chromatography (SiO2; ethyl acetate/CH3OH, 19:1) yields the title compound: m.p.: 132-134° C.; Anal. calc.(C21H17N4Cl.½CH3OH) C, 68.52%; H, 5.08%; N, 14.87%. found. C, 68.4%; H, 5.0%; N, 14.9%.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US06710047B2uspto-grants-2004_03