Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1089918Erstellt: 26. Oktober 2026

Sodium Iodide → 10-(3-diethylamino-propylamino) 5H-pyrido[3',4':4,5]pyrrolo[2,3-g]isoquinoline

https://huagongshe.com/reaction/1089918

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium IodideHCID 5238—
Eduktp-Toluenesulfonic acidHCID 6101—
EduktChlorotrimethylsilaneHCID 6397—
EduktHexamethyldisilazaneHCID 13838—
EduktN,N-Diethyl-1,3-propanediamineHCID 61011—
Edukt10-methoxy 6-methyl 5H-pyrido[3',4':4,5]pyrrolo[2,3-g]isoquinolineHCID 11021716—
LösungsmittelAcetonitrileHCID 6342—
Produkt10-(3-diethylamino-propylamino) 5H-pyrido[3',4':4,5]pyrrolo[2,3-g]isoquinolineHCID 57067349—

Reaktionsschritte

0.87 g (0.0033 mole) of 10-methoxy 6-methyl 5H-pyrido[3',4':4,5]pyrrolo[2,3-g]isoquinoline and 0.495 g (0.003 mole) of sodium iodide are suspended in 25 ml of acetonitrile and 4.2 ml (0.33 mole) of trimethylsilylchloride, and then heated at 40° C. for 17 hours. 10.5 ml (0.050 mole) of hexamethyldisilazane, 0.113 g (6×10-4 mole) of anhydrous p-toluenesulfonic acid and 22.4 ml (0.14 mole) of diethylaminopropylamine are then added. After distillation of the acetonitrile, the mixture is heated at reflux for 20 hours. It is evaporated to dryness under a partial vacuum and the residue is stirred with 20 ml of water and 5 ml of diisopropyl ether for 1 hour. The precipitate obtained is filtered off and dried under vacuum at 50° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05079363
Quelldatensatzuspto-grants-1992_01
ORD IDord-e86c1c5b169b4ebeb61e406073a700ff
Quellennotizuspto-grants-1992_01