Reaktion #3510

ord-2f0d5340aaf840a58a389a03ef389f8c

Reaktionsgleichung

COc1ccc(-c2cc3cnc(N)nc3nc2Cl)cc1
2-amino-7-chloro-6-(4-methoxyphenyl)-pyrido[2,3-d]pyrimidine
COc1ccc(-c2cc3cnc(N)nc3nc2Cl)cc1
2-Amino-7-chloro-6-(4-methoxyphenyl)-pyrido[2,3-d]-pyrimidine
CN
methylamine
CNc1nc2nc(N)ncc2cc1-c1ccc(OC)cc1
title compound
CNc1nc2nc(N)ncc2cc1-c1ccc(OC)cc1
6-(4-Methoxyphenyl)-N7 -methyl-pyrido[2,3-d]pyrimidine-2,7-diamine

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturwere heated in a bomb on a steam bath for 4 hours
  2. 2
    TemperaturAfter cooling
  3. 3
    Waschenthe suspension was washed out of the bomb with 50 mL of methanol/water (50:50)
  4. 4
    Sonstigethe solvents were evaporated in vacuo
  5. 5
    Filtrationfiltered
  6. 6
    Sonstigecrystallized from ethanol

Vorschrift

A mixture of 3.4 g of 2-amino-7-chloro-6-(4-methoxyphenyl)-pyrido[2,3-d]pyrimidine from Example 12, 40 mL of anhydrous methylamine, and 10 mL of methanol were heated in a bomb on a steam bath for 4 hours. After cooling, the suspension was washed out of the bomb with 50 mL of methanol/water (50:50) and the solvents were evaporated in vacuo. The solid residue was slurried with 50 mL of water, filtered, and crystallized from ethanol to afford 2.2 g of the title compound 6-(4-methoxyphenyl)-N7 -methyl-pyrido[2,3-d]pyrimidine-2,7-diamine, mp 270°-275° C. dec.

Quelle

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