Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1796609Erstellt: 26. Oktober 2026

N-acetylanthranilic acid → 5-Methyl-6-(2-methyl-4-oxo-4H-quinazolin-3-yl)-4-(4-phenoxy-phenylamino)-pyrrolo[1,2-b]pyridazine-3-carbonitrile

https://huagongshe.com/reaction/1796609

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktN-acetylanthranilic acidHCID 6971—
EduktDiisopropylethylamineHCID 81531—
EduktPyBOPHCID 2724699—
Edukt6-Amino-5-methyl-4-(4-phenoxy-phenylamino)-pyrrolo[1,2-b]pyridazine-3-carbonitrile hydrochlorideHCID 22179487—
Lösungsmittel1,2-DichloroethaneHCID 11—
Produkt5-Methyl-6-(2-methyl-4-oxo-4H-quinazolin-3-yl)-4-(4-phenoxy-phenylamino)-pyrrolo[1,2-b]pyridazine-3-carbonitrileHCID 22179517—

Reaktionsschritte

6-Amino-5-methyl-4-(4-phenoxy-phenylamino)-pyrrolo[1,2-b]pyridazine-3-carbonitrile hydrochloride (10.4 mg, 0.027 mmol), 2-acetylamino benzoic acid (7 mg, 0.04 mmol), PyBOP (21 mg, 0.04 mmol) and DIEA (8.6 mg, 0.067 mmol) in 1.2-dichloroethane (0.5 ml) were stirred at RT for 16 hrs. The reaction mixture was concentrated and purified by silica gel flash chromatography to isolate 375 as a yellow film (5.8 mg, 42%). [M+H]+=498.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07030112B2
Quelldatensatzuspto-grants-2006_04
ORD IDord-ec285a38b7bb45b8a73d88a8383359ef
Quellennotizuspto-grants-2006_04