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HRID 1194677Erstellt: 26. Oktober 2026

Ici 109,081 → 6-(4-(3-tert.-Butoxycarbonyl-thiazolidin-2-yl-carbonyl-amino)-phenyl)-5-methyl-4,5-dihydro-3(2H)-pyridazinone

https://huagongshe.com/reaction/1194677

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktIci 109,081HCID 161928—
Edukt3-(tert-Butoxycarbonyl)-1,3-thiazolidine-2-carboxylic acidHCID 4644094—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt6-(4-(3-tert.-Butoxycarbonyl-thiazolidin-2-yl-carbonyl-amino)-phenyl)-5-methyl-4,5-dihydro-3(2H)-pyridazinoneHCID 13749452—

Reaktionsschritte

7.5 g (0.032 mole) of 3-tert.-butoxycarbonyl-thiazolidine-2-carboxylic acid and 5.2 g (0.032 mole) of N,N'-carbonyl-diimidazole are heated under reflux in 50 ml of tetrahydrofuran for 15 minutes. After addition of 6.1 g (0.03 mole) of 6-(4-aminophenyl)-5-methyl-4,5-dihydro-3(2H)-pyridazinone, the mixture is stirred at room temperature for 18 hours and concentrated and the residue is crystallised with ethyl acetate.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04816454
Quelldatensatzuspto-grants-1989_03
ORD IDord-037762da13f34779ab8b615cc771aa53
Quellennotizuspto-grants-1989_03