Реакция #1605849

Уравнение реакции

chloromethyl 7-(4-(4-(2,3-dichlorophenyl)piperazin-1-yl)butoxy)-2-oxo-3,4-dihydroquinoline-1(2H)-carboxylate

palmitic acid

cesium carbonate

→

palmitoyloxymethyl 7-(4-(4-(2,3-dichlorophenyl)piperazin-1-yl)butoxy)-2-oxo-3,4-dihydroquinoline-1(2H)-carboxylate

Растворители

dimethyl formamide

ethyl acetate

Условия реакции

Обработка

1. 1
   Температураto cool to room temperature
2. 2
   Промывкаwashed with 1:1 water/brine (3×40 mL)
3. 3
   ФильтрацияThe organics were filtered
4. 4
   Другоеto remove a white precipitate
5. 5
   Сушкаthen dried (MgSO4)
6. 6
   Концентрированиеconcentrated
7. 7
   ДругоеThe crude product was purified by column chromatography on silica eluting with 0.5% Et3N/ethyl acetate

Методика

To a solution of chloromethyl 7-(4-(4-(2,3-dichlorophenyl)piperazin-1-yl)butoxy)-2-oxo-3,4-dihydroquinoline-1(2H)-carboxylate (1.16 g, 2.14 mmol) in dimethyl formamide (20 mL) was added palmitic acid (825 mg, 3.22 mmol) and cesium carbonate (524 mg, 1.61 mmol). The reaction was heated to 60° C. for 5 hours then allowed to cool to room temperature. The reaction was diluted with ethyl acetate (20 mL) and washed with 1:1 water/brine (3×40 mL). The organics were filtered to remove a white precipitate then dried (MgSO4) and concentrated. The crude product was purified by column chromatography on silica eluting with 0.5% Et3N/ethyl acetate to give palmitoyloxymethyl 7-(4-(4-(2,3-dichlorophenyl)piperazin-1-yl)butoxy)-2-oxo-3,4-dihydroquinoline-1(2H)-carboxylate, Compound-89 (548 mg, 32% over 2 steps). The material was determined to be 83% pure by LCMS.

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