Réaction #452429

Équation de réaction

hydrochloric acid

hexane

4-(4-fluorobenzoyl)aminophenylhydrazine

5-phthalimidyl-2-pentanone

hydrochloric acid

→

product

Rendement 6.6%

N-[2-methyl-3-(2-phthalimidylethyl)-1H-indol-5-yl]-4-fluoro-benzamide

Rendement 6.6%

Solvants

ethanol

Conditions de réaction

Traitement

1. 1
   Températureheating
2. 2
   TempératureThe reaction mixture was then cooled to 0° C.
3. 3
   AutreThe solid which formed
4. 4
   Filtrationwas filtered
5. 5
   Lavagewashed with hexane
6. 6
   Autreprovided
7. 7
   Autreafter drying
8. 8
   ConcentrationThe mother liquor was concentrated under reduced pressure
9. 9
   Lavageeluting with 1:1 hexane
10. 10
    workup.ADDITIONFractions containing product
11. 11
    Concentrationconcentrated under reduced pressure

Mode opératoire

To a solution of 5.33 gm (21.7 mMol) 4-(4-fluorobenzoyl)aminophenylhydrazine and 5.03 gm (21.8 mMol) 5-phthalimidyl-2-pentanone in 100 mL ethanol were added 2 mL concentrated hydrochloric acid and the reaction mixture was heated at 80° C. for 14 hours. To the reaction mixture were then added an additional 3 mL concentrated hydrochloric acid and heating continued for an additional 6 hours. The reaction mixture was then cooled to 0° C. and 100 mL hexane were slowly added. The solid which formed was filtered and washed with hexane and provided, after drying, 6.67 gm of the desired compound. The mother liquor was concentrated under reduced pressure and then subjected to silica gel chromatography, eluting with 1:1 hexane:ethyl acetate. Fractions containing product were combined and concentrated under reduced pressure to provide an additional 0.63 gm of product. Overall yield was 7.3 gm (76%).

Source