Reaktion #3509

ord-86096de2e5674031bab10b49fa871e15

Reaktionsgleichung

COc1ccc(-c2cc3cnc(N=CN(C)C)nc3nc2Cl)cc1
N'-(7-chloro-6-(4-methoxy-phenyl)-pyrido[2,3-d]pyrimidin-2-yl)-N,N-dimethyl-formamidine
COc1ccc(-c2cc3cnc(N=CN(C)C)nc3nc2Cl)cc1
N'-(7-Chloro-6-(4-methoxyphenyl)-pyrido[2,3-d]pyrimidin-2-yl)-N,N-dimethyl-formamidine
COc1ccc(-c2cc3cnc(N)nc3nc2Cl)cc1
title compound
Ausbeute 32.2%
COc1ccc(-c2cc3cnc(N)nc3nc2Cl)cc1
2-Amino-7-chloro-6-(4-methoxyphenyl)-pyrido[2,3-d]-pyrimidine
Ausbeute 32.2%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturwas refluxed for 3 hours
  2. 2
    EinengenThe solution was concentrated in vacuo
  3. 3
    Filtrationthe precipitate collected by filtration
  4. 4
    SonstigeCrystallization from ethanol

Vorschrift

A mixture of 10 g of N'-(7-chloro-6-(4-methoxy-phenyl)-pyrido[2,3-d]pyrimidin-2-yl)-N,N-dimethyl-formamidine from Example 11 and 500 mL of 95% ethanol was refluxed for 3 hours. The solution was concentrated in vacuo and the precipitate collected by filtration. Crystallization from ethanol afforded 2.7 g of the title compound 2-amino-7-chloro-6-(4-methoxyphenyl)-pyrido[2,3-d]pyrimidine, mp 275°-280° C. dec.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05733913uspto-grants-1998_03