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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1874503Erstellt: 24. Oktober 2026

Tetrahydrofuran → N-[2-chloro-5-({2-[(cyclopropylcarbonyl)amino][1,2,4]triazolo[1,5-a]pyridin-6-yl}oxy)phenyl]-1-ethyl-3-methyl-1H-pyrazole-5-carboxamide

https://huagongshe.com/reaction/1874503

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTetrahydrofuranHCID 8028—
EduktThionyl ChlorideHCID 24386—
Edukt1-Ethyl-3-methyl-1H-pyrazole-5-carboxylic acidHCID 2743794—
EduktN-[6-(3-amino-4-chlorophenoxy)[1,2,4]triazolo[1,5-a]pyridin-2-yl]cyclopropanecarboxamideHCID 57749285—
KatalysatorDimethylformamideHCID 6228—
LösungsmittelDimethylacetamideHCID 31374—
ProduktN-[2-chloro-5-({2-[(cyclopropylcarbonyl)amino][1,2,4]triazolo[1,5-a]pyridin-6-yl}oxy)phenyl]-1-ethyl-3-methyl-1H-pyrazole-5-carboxamideHCID 5774933741%

Reaktionsschritte

In the same manner as in Example 55 and using 1-ethyl-3-methyl-1H-pyrazole-5-carboxylic acid (56.2 mg, 0.365 mmol), tetrahydrofuran (5 mL), thionyl chloride (63.3 μL, 0.730 mmol), N,N-dimethylformamide (2 drops), N-[6-(3-amino-4-chlorophenoxy)[1,2,4]triazolo[1,5-a]pyridin-2-yl]cyclopropanecarboxamide (114 mg, 0.332 mmol) and N,N-dimethylacetamide (6 mL) as starting materials, the title compound (65.2 mg, 41%) was obtained as a white solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08304557B2
Quelldatensatzuspto-grants-2012_11
ORD IDord-3d56b9c770b34ff387bb7c1f55594ed7
Quellennotizuspto-grants-2012_11