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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 850921Erstellt: 25. Oktober 2026

Isopropylamine → Indecainide

https://huagongshe.com/reaction/850921

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktIsopropylamineHCID 6363—
Edukt9-(2-Cyanoethyl)-9H-fluorene-9-carboxamideHCID 3018819—
EduktHCID 178418361HCID 178418361—
KatalysatorPalladiumHCID 23938—
ProduktIndecainideHCID 5219560%

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

A mixture of 500 g. of 9-aminocarbonyl-9-(2-cyanoethyl)fluorene, 1500 ml. of isopropylamine and 100 g. of 5% palladium on carbon was placed in a one gallon high pressure hydrogenation bomb. The bomb was pressurized with hydrogen to a pressure of 1500 psi, and the reaction mixture was then stirred at 100° C. for ten hours, and for an additional eight hours at room temperature. The reaction mixture was filtered to remove the hydrogenation catalyst, and the solvent was removed from the filtrate by evaporation under reduced pressure. The residue was dissolved in ethyl acetate, and the solution was extracted several times with 1 N hydrochloric acid. The acidic extracts were combined, made alkaline by the addition of sodium hydroxide, and the alkaline mixture was extracted with fresh ethyl acetate. The organic layer was separated, washed with water and dried. Removal of the solvent by evaporation under reduced pressure provided 9-(3-isopropylaminopropyl)-9-aminocarbonylfluorene as a solid residue. The solid was dissolved in methanol and treated with anhydrous hydrogen chloride. The crystalline product which formed was recrystallized from chloroform to afford 391 g. of 9-(3-isopropylaminopropyl)-9-aminocarbonylfluorene hydrochloride. Yield 60%. m.p. 216.5°-217° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04382093
Quelldatensatzuspto-grants-1983_05
ORD IDord-d0b858b19265490f8cc2a03d9c9b9882
Quellennotizuspto-grants-1983_05