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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 280059Erstellt: 25. Oktober 2026

Ammonia → furo(3,4-b)pyridin-5(7H)-one

https://huagongshe.com/reaction/280059

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAmmoniaHCID 222—
EduktAcetic AnhydrideHCID 7918—
EduktFuro[3,4-b]pyridine-5,7-dioneHCID 69688—
EduktN,N-Diethyl-m-phenetidineHCID 74625—
Edukt1H-Indole, 1-ethyl-2-methyl-HCID 170432—
KatalysatorZincchlorideHCID 3007855—
LösungsmittelAcetic AcidHCID 176—
LösungsmittelWaterHCID 962—
LösungsmittelIsopropanolHCID 3776—
Produktfuro(3,4-b)pyridin-5(7H)-oneHCID 819439258,8%

Reaktionsschritte

20.0 g of quinolinic anhydride, 80 ml of acetic acid, 20.3 g of N-ethyl-2-methylindole and 2.74 g of zinc chloride are stirred at 20° C. for 5 hours. 23.6 g of 3-(N,N-diethylamino)-phenetole and 30 ml of acetic anhydride are then added, after which the reaction mixture is warmed to 50° to 60° C. and stirred at this temperature for 2 hours. After addition of 170 ml of 30% aqueous ammonia and 100 ml of water, the product precipitates as a paste and is isolated. 160 ml of isopropanol are added to the paste and the mixture is refluxed for 1 hour. After cooling, the recrystallised product is filtered off, washed with isopropanol and dried, affording 46.9 g of the isomer-free 4-azaphthalide compound of the formula ##STR15## of melting point 156° to 158° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04587539
Quelldatensatzuspto-grants-1986_05
ORD IDord-96ff3c0d8cde44bca4cbc6c9fb34e7c3
Quellennotizuspto-grants-1986_05