Реакция #567622

ord-da205d230cc641cd84c46f1bc5610e96

Уравнение реакции

Cc1cccc(-c2c(-c3ccncc3)nc(Cl)n(C)c2=O)c1
2-chloro-3-methyl-5-(3-methylphenyl)-6-(4-pyridyl)-4(3H)-pyrimidinone
CC(C)(CN)C(N)c1ccccc1
3-phenyl-2,2-dimethyl-1,3-propanediamine
Cc1cccc(-c2c(-c3ccncc3)nc(NCC(C)(C)C(N)c3ccccc3)n(C)c2=O)c1.Cl
2-((-3-Amino-2,2-dimethyl-3-phenylpropyl)-amino)-3-methyl-5-(3-methylphenyl)-6-(4-pyridyl)-4(3H)-pyrimidinone hydrochloride

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ДругоеThe solvent was evaporated
  2. 2
    Другоеthe crude product purified by column chromatography on silica gel

Методика

A solution of 2-chloro-3-methyl-5-(3-methylphenyl)-6-(4-pyridyl)-4(3H)-pyrimidinone (228 mg, 0.73 mmol) and 3-phenyl-2,2-dimethyl-1,3-propanediamine (178 mg, 1 mmol) (prepared according to: W. Ten Hoeve and H. Wynberg, Synth. Commun. 24 (15), 2215-2221, 1994) in ethanol (4 ml) was stirred at room temperature for 16 h. The solvent was evaporated and the crude product purified by column chromatography on silica gel. MS (m/z): 454 (M+H)+; C28H31N5O requir. 453.6 (free base).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US06649604B2uspto-grants-2003_11