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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1586202Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/1586202

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktHexaneHCID 8058—
Edukt2-(4-Oxopentyl)-1H-isoindole-1,3(2H)-dioneHCID 236270—
Edukt4-(4-Fluorobenzoyl)aminophenylhydrazineHCID 11831684—
LösungsmittelEthanolHCID 702—
ProduktN-[2-methyl-3-(2-phthalimidylethyl)-1H-indol-5-yl]-4-fluoro-benzamideHCID 232904766,6%

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

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%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05942536
Quelldatensatzuspto-grants-1999_08
ORD IDord-819c94266a2841929f7934dcc8ce59c6
Quellennotizuspto-grants-1999_08