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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1874493Erstellt: 27. Oktober 2026

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

https://huagongshe.com/reaction/1874493

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTetrahydrofuranHCID 8028—
EduktThionyl ChlorideHCID 24386—
Edukt1,3-dimethyl-1H-pyrazole-4-carboxylic acidHCID 1273304—
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]-1,3-dimethyl-1H-pyrazole-4-carboxamideHCID 5774920824,3%

Reaktionsschritte

In the same manner as in Example 55 and using 1,3-dimethyl-1H-pyrazole-4-carboxylic acid (58.2 mg, 0.415 mmol), tetrahydrofuran (5 mL), thionyl chloride (71.7 μL, 0.826 mmol), N,N-dimethylformamide (2 drops), N-[6-(3-amino-4-chlorophenoxy)[1,2,4]triazolo[1,5-a]pyridin-2-yl]cyclopropanecarboxamide (129 mg, 0.375 mmol) and N,N-dimethylacetamide (6 mL) as starting materials, the title compound (42.5 mg, 24%) was obtained as a white solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08304557B2
Quelldatensatzuspto-grants-2012_11
ORD IDord-ec0a5d413a524e67894395e6d680fea3
Quellennotizuspto-grants-2012_11