Reacción #62022

Ecuación de reacción

5-(4-Isopropyl-piperazine-1-carbonyl)-furan-2-carbaldehyde

Vilsmeier reagent

1-isopropyl-piperizine dihydrochloride

5-formyl-2-furancarboxylic acid

→

desired product

Rendimiento 87.0%

(4-Isopropyl-piperazin-1-yl)-(5-piperidin-1-ylmethyl-furan-2-yl)-methanone

Rendimiento 87.0%

Disolventes

DCM

DCM

Condiciones de reacción

Tratamiento posterior

1. 1
   workup.STIRRINGthe combined mixture was stirred at 0° C. for 30 min
2. 2
   TemperaturaThe mixture was warmed to rt
3. 3
   workup.STIRRINGstirred for another 1.5 h
4. 4
   Filtraciónfiltered
5. 5
   workup.ADDITIONThe filtrate (containing 5-formyl-furan-2-carbonyl chloride)
6. 6
   Temperaturamaintained at 0° C
7. 7
   Temperaturawas warmed to rt
8. 8
   workup.STIRRINGstirred for 30 min
9. 9
   FiltraciónThe reaction mixture was filtered
10. 10
    Temperaturathe filtrate was cooled to 0° C
11. 11
    workup.ADDITIONThis second filtrate was then treated dropwise with the previously prepared solution of 5-formyl-furan-2-carbonyl chloride at 0° C
12. 12
    workup.STIRRINGThe combined mixture was stirred at 0° C. for 30 min
13. 13
    TemperaturaThe reaction mixture was cooled to 0° C.
14. 14
    Filtraciónfiltered
15. 15
    Lavadothe filtrate was washed with H2O (2×15 mL), 0.5 N NaOH (1×15 mL)
16. 16
    OtroThe organic layer was separated
17. 17
    Secadodried over anhydrous Na2SO4
18. 18
    Filtraciónfiltered
19. 19
    Concentraciónconcentrated

Procedimiento

5-(4-Isopropyl-piperazine-1-carbonyl)-furan-2-carbaldehyde. Vilsmeier reagent [(chloromethylene)dimethylammonium chloride, 0.820 g, 6.43 mmol] was suspended in DCM (30 mL) under nitrogen with stirring and cooled to 0° C. To this suspension was added 5-formyl-2-furancarboxylic acid (0.900 g, 6.43 mmol) and the combined mixture was stirred at 0° C. for 30 min. The mixture was warmed to rt, stirred for another 1.5 h, and filtered. The filtrate (containing 5-formyl-furan-2-carbonyl chloride) was set aside and maintained at 0° C. In a second flask, 1-isopropyl-piperizine dihydrochloride (1.28 g, 6.37 mmol) in DCM (15 mL) was cooled to 0° C. The solution was treated with TEA (2.250 g, 22.30 mmol) slowly and then was warmed to rt and stirred for 30 min. The reaction mixture was filtered and the filtrate was cooled to 0° C. This second filtrate was then treated dropwise with the previously prepared solution of 5-formyl-furan-2-carbonyl chloride at 0° C. The combined mixture was stirred at 0° C. for 30 min and then at rt for 1 h. The reaction mixture was cooled to 0° C. and filtered, and the filtrate was washed with H2O (2×15 mL), 0.5 N NaOH (1×15 mL), and satd. aq. NaCl (1×15 mL). The organic layer was separated, dried over anhydrous Na2SO4, filtered, and concentrated to yield the desired product (1.40 g, 87%).

Fuente