Реакция #1549

ord-c771bb9653f84a339085fb2d456f388e

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Температураto warm
  2. 2
    workup.ADDITIONafter each addition
  3. 3
    ДругоеThe solvent was removed in vacuo
  4. 4
    Промывкаwashed twice with water
  5. 5
    СушкаThe organic layer was dried over MgSO4
  6. 6
    Концентрированиеconcentrated
  7. 7
    Другоеto yield 1.15 g crude solid product

Методика

To an ice cooled solution of 1.5 g (3.8 mmol) 6-chloro-5-methyl-2-phenyl-3-propargyl-4(3H)-pyrimidinone in 4 mL of tetrahydrofuran, was added 22 mL (99 mmol) of 4.5M dimethylamine in ether portionwise (2-4 mL) over a period of 7 days. The reaction mixture was allowed to warm and stir at room temperature after each addition. The progress of the reaction was followed by gas chromatography and proceeded to 80% completion. The solvent was removed in vacuo and the residue was taken up in ether and washed twice with water. The organic layer was dried over MgSO4 and concentrated to yield 1.15 g crude solid product. Flash column chromatography on silica gel (gradient elution 25-30% ethyl acetate-hexane) afforded pure 6-dimethylamino-5-methyl-2-phenyl-3-propargyl-4(3H)-pyrimidinone (compound 23), as a white solid. 1H-NMR (CDCl3) δ 2.2(3H,s); 2.35(1H,t); 3.5(6H,s); 4.6(2H,d); 7.65(3H,m); 7.75(2H,m).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US05726124uspto-grants-1998_03