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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2391395Erstellt: 23. Oktober 2026

Tetrahydrofuran → N-{5-[(2-{[(2,2-difluorocyclopropyl)carbonyl]amino]imidazo[1,2-b]pyridazin-6-yl)oxy]-2-methylphenyl}-1,3-dimethyl-1H-pyrazole-5-carboxamide

https://huagongshe.com/de/reaction/2391395

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTetrahydrofuranHCID 8028—
EduktOxalyl chlorideHCID 65578—
Edukt2,2-Difluorocyclopropane-1-carboxylic acidHCID 2782823—
EduktN-{5-[(2-aminoimidazo[1,2-b]pyridazin-6-yl)oxy]-2-methylphenyl)-1,3-dimethyl-1H-pyrazole-5-carboxamide hydrochlorideHCID 57505635—
KatalysatorDimethylformamideHCID 6228—
LösungsmittelDimethylacetamideHCID 31374—
ProduktN-{5-[(2-{[(2,2-difluorocyclopropyl)carbonyl]amino]imidazo[1,2-b]pyridazin-6-yl)oxy]-2-methylphenyl}-1,3-dimethyl-1H-pyrazole-5-carboxamideHCID 5750563473%

Reaktionsschritte

In the same manner as in Example 259 and using 2,2-difluorocyclopropanecarboxylic acid (88 mg, 0.60 mmol), tetrahydrofuran (5 mL), N,N-dimethylformamide (1 drop), oxalyl chloride (74 μL, 0.86 mmol), N-{5-[(2-aminoimidazo[1,2-b]pyridazin-6-yl)oxy]-2-methylphenyl}-1,3-dimethyl-1H-pyrazole-5-carboxamide hydrochloride (250 mg, 0.60 mmol) and N,N-dimethylacetamide (7 mL) as starting materials, the title compound (210 mg, 73%) was obtained as a white solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08273741B2
Quelldatensatzuspto-grants-2012_09
ORD IDord-968e8131afb64e3d92c9b0694979bcea
Quellennotizuspto-grants-2012_09