反応 #2298647

ord-d031a43d6fc24256b868b2415fd79acb

反応方程式

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
収率 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
収率 125.7%

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    ろ過the resultant crystalline compound was filtered
  2. 2
    洗浄washed with water
  3. 3
    その他dried

実験手順

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.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: USRE039266E1uspto-grants-2006_09