Реакция #2298647

ord-d031a43d6fc24256b868b2415fd79acb

Уравнение реакции

CCCc1nc(C)cc(=O)n1CCOc1ccc(C=O)cc1
4-[2-[4-methyl-2-propyl-6-oxo-1,6-dihydro-1-pyrimidinyl]ethoxy]benzaldehyde
O=C1CSC(=O)N1
thiazolidine-2,4-dione
O=C(O)c1ccccc1
benzoic acid
C1CCNCC1
piperidine
CCCc1nc(C)cc(=O)n1CCOc1ccc(C=C2SC(=O)NC2=O)cc1
title compound
Выход 125.7%
CCCc1nc(C)cc(=O)n1CCOc1ccc(C=C2SC(=O)NC2=O)cc1
5-[4-[2-[4-Methyl-2-propyl-6-oxo-1,6-dihydro-1-pyrimidinyl]ethoxy]phenyl methylene]thiazolidine-2,4-dione
Выход 125.7%

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Фильтрацияthe resultant crystalline compound was filtered
  2. 2
    Промывкаwashed with water
  3. 3
    Другоеdried

Методика

A mixture of 4-[2-[4-methyl-2-propyl-6-oxo-1,6-dihydro-1-pyrimidinyl]ethoxy]benzaldehyde (10 g, 24.5 mmol) (obtained from preparation 1), thiazolidine-2,4-dione (3.5 g, 30 mmol), benzoic acid (388 mg, 3.18 mmol) and piperidine (352 μl, 303 mg, 3.68 mmol) in toluene (50 ml) was refluxed for 1 h with continuous removal of water. The reaction was cooled to room temperature and the resultant crystalline compound was filtered and washed with water and dried to afford the title compound (12.3 g, 99%), mp 240-242° C.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: USRE039266E1uspto-grants-2006_09