Реакция #967241

ord-5af3bbcee42c41e2b22d58501a91ab67

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Концентрированиеis then concentrated under reduced pressure
  2. 2
    workup.ADDITIONWater and ethyl acetate are added
  3. 3
    workup.STIRRINGthe resulting mixture is thus stirred for 30 minutes
  4. 4
    ДругоеThe precipitate formed
  5. 5
    Фильтрацияis filtered off
  6. 6
    Промывкаrinsed with ethyl ether
  7. 7
    Другоеdried in a rotary evaporator
  8. 8
    ДругоеAfter purification by silica column chromatography as a solid deposit, eluent
  9. 9
    Другоеdichloromethanemethanol 95/05, a solid is obtained which
  10. 10
    ФильтрацияThe solid is filtered off
  11. 11
    Другоеdried

Методика

0.160 ml of pyridine, 240 mg of N-[3-(dimethylamino)propyl]-N′-ethylcarbodiimide hydrochloride and 400 mg of N, N-dimethyl-m-phenylenediamine are added to a solution of 250 mg of sodium [4-(morpholin-4-yl)-6-oxo-1,6-dihydropyrimidin-2-yl]acetate prepared in stage 2 of Example 1 in 4 ml of N,N-dimethylformamide. The reaction mixture is stirred at ambient temperature overnight and is then concentrated under reduced pressure. Water and ethyl acetate are added and the resulting mixture is thus stirred for 30 minutes. The precipitate formed is filtered off, rinsed with ethyl ether and dried in a rotary evaporator. After purification by silica column chromatography as a solid deposit, eluent: dichloromethanemethanol 95/05, a solid is obtained which is taken up in a mixture of dichloromethane, methanol and ethyl ether. The solid is filtered off and dried. 30 mg of N-[3-(dimethylamino)phenyl]-2-[4-(morpholin-4-yl)-6-oxo-1,6-dihydropyrimidin-2-yl]acetamide are obtained in the form of a yellow solid, the characteristics of which are the following:

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US08993565B2uspto-grants-2015_03